Clinical Trial Details
— Status: Not yet recruiting
Administrative data
| NCT number |
NCT06303076 |
| Other study ID # |
134 |
| Secondary ID |
|
| Status |
Not yet recruiting |
| Phase |
Phase 4
|
| First received |
|
| Last updated |
|
| Start date |
September 2024 |
| Est. completion date |
December 2026 |
Study information
| Verified date |
March 2024 |
| Source |
Sultan Qaboos University |
| Contact |
Mohammed Al Alawi, MD PhD |
| Phone |
+96892281145 |
| Email |
alalawim[@]squ.edu.om |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
The study's primary objective is to evaluate the effectiveness of Tinazidine compared to
Zolpidem in enhancing sleep quality, with secondary objectives including the assessment of
adverse effects, safety profile, and patient tolerance with each treatment. The trial will be
conducted as a double-blind RCT, with participants randomly assigned to receive either
Tinazidine (0.1 mg/Kg/HS) or Zolpidem 10 mg HS, for 12 weeks. Eligible participants, aged
18-60 years, diagnosed with primary insomnia as per DSM-5 criteria, will be recruited from an
outpatient sleep clinic affiliated with Al-Masara Hospital. Data on sleep quality, and side
effects, will be collected using the Sleep Pittsburgh Sleep Quality Index (PSQI), Clinical
Global Impression (CGI), sleep diaries, actigraphy, polysomnography, and regular clinical
interview though OPD follow-up visits. The primary outcome considered was the mean global
PSQI score before and after the treatment. The primary outcome will be measured four times
(baseline, 4 weeks, 8 weeks, and 12 weeks), We considered an attrition rate (dropout/lost
follow-up) of 10%. Therefore, the sample size is 90 subjects (45 in each group). Group
comparisons for mean scores will be conducted using independent samples t-tests, and
within-group comparisons will be assessed using paired samples t-tests. Changes in sleep
quality over time between treatment groups will be evaluated using repeated measures ANOVA.
Associations between categorical variables will be examined using Chi-square tests (including
Fisher's exact or Likelihood ratio tests as appropriate). Statistical significance will be
considered for p-values less than 0.05. All analyses will be performed using IBM SPSS
Statistics (Version 29.0). The findings of this study seek to elucidate the comparative
efficacy and safety profiles of Tizanidine and Zolpidem in treating primary insomnia. The
study aims to offer insights into the effectiveness of Tizanidine versus Zolpidem in
improving sleep quality among patients with primary insomnia. Through the evaluation of
efficacy, adverse effects, and safety profiles. This study aims to inform clinicians and
healthcare practitioners about the optimal treatment choices for individuals with primary
insomnia.
Description:
Efficacy of Tizanidine (0.1 mg/Kg/HS) versus Zolpidem 10 mg HS in Primary Insomnia: Double
Blind Randomized Controlled Trial
Literature review:
Insomnia: Prevalence and Impact
Around 10% of adults have an insomnia disorder, while another 20% experience occasional
insomnia symptoms (1). Women, older adults, and those facing socioeconomic challenges are
more prone to insomnia. Insomnia often persists over time, with a 40% persistence rate over
five years (1). Insomnia is a significant public health concern requiring individual clinical
care and broad population-level interventions to improve sleep health (1).
The Individual and Public Health Ramifications of Insomnia
On an individual level, insomnia has significant repercussions on daily life, including
impaired daytime function, emotional distress, reduced productivity, increased healthcare
utilization, and heightened accident risk (2). Along with physiological hyperarousal,
cardiometabolic morbidities such as hypertension, and diabetes, neurocognitive impairment
such as short-term memory impairment, and psychological impairment such as depression, and
anxiety (2)(3). Additionally, untreated insomnia tends not to improve over time (3).
On a public level, insomnia impacts various aspects of society. It contributes to an
increased economic burden through decreased work productivity and higher healthcare costs due
to increased healthcare service utilization (4). Additionally, insomnia heightens the risk of
accidents, including traffic accidents, jeopardizing public safety (4). Its association with
mental health disorders adds to the healthcare burden of managing these conditions, while the
increased risk of chronic medical diseases further strains healthcare systems (5). Given that
the untreated economic costs of insomnia far exceed that of treated insomnia (4), efforts
should be focused on developing clinical trials aimed at assessing the cost-benefit, and
cost-effectiveness of various insomnia therapies.
Defining Primary Insomnia According to DSM-5 Criteria
Primary insomnia, as defined in the DSM-5 criteria (6), refers to a sleep disorder
characterized by difficulty initiating or maintaining sleep, or experiencing non-restorative
sleep, for at least one month. Individuals with primary insomnia often report significant
distress or impairment in social, occupational, or other important areas of functioning due
to their sleep difficulties. The DSM-5 criteria further specify that insomnia is not better
explained by another sleep disorder, such as narcolepsy, or circadian rhythm sleep disorder,
etc., and not due to another mental disorder. Additionally, the diagnosis of primary insomnia
requires that the sleep disturbance does not occur due to the physiological effect of a
medical condition or substance use (6).
Current FDA-Approved Medications for Insomnia
Current FDA-approved medications for insomnia include benzodiazepines, such as Triazolam, and
Temazepam, as well as non-benzodiazepines (Z drug) such as zolpidem, and zaleplon.
Additionally, melatonin agonist ramelteon, tricyclic antidepressant doxepin, and orexin
antagonists such as suvorexant are also among the approved options for managing insomnia (7).
Zolpidem was the first Z drug to be developed. In studies investigating zolpidem adverse
events that arose during treatment, such as drowsiness, nausea, dizziness, nightmares, and
agitation, have led to the discontinuation of the zolpidem (7). Additionally, some patients
experienced anterograde amnesia (7). Moreover, concerns about the frequent use of
benzodiazepine for insomnia include the risk of dependence, drug-seeking behavior, and abuse
in the context of inadequate medical supervision (8). Evaluating any new pharmacological
treatments against conventional benzodiazepine and z-drugs intake is crucial, as there is
limited data on the benefit-to-risk ratio of such treatment strategies, necessitating
head-to-head trials.
Therapeutic Applications of Tizanidine
Tizanidine, a centrally acting alpha-2 agonist, is commonly prescribed to manage spasticity
induced by conditions such as multiple sclerosis, stroke, and spinal cord injury. Beyond its
labeled indications, it finds off-label use in alleviating chronic neck and back pain as well
as chronic migraines (9).
Clinical Trials of Tizanidine in the Context of Insomnia
Tizanidine has shown promise in previous studies for its efficacy in sleep disturbances. In a
study where 24 subjects with Myofascial pain syndrome received tizanidine, which was titrated
up to 12 mg over 3 weeks and maintained for 2 weeks. the study results showed Pain intensity
and disability decreased significantly from baseline at weeks 3 and 5 and after washout (P <
.001). Pressure threshold and sleep improved for all study periods (P < .001). The Sleep in
this study was assessed via a visual analog scale (VAS) (10).
In a randomized controlled clinical trial assessing the efficacy of adding either tizanidine
or cyclobenzaprine in treating jaw pain, 45 patients diagnosed with myofascial pain were
randomly assigned to three groups: a placebo group, a tizanidine group (4 mg), and a
cyclobenzaprine group (10 mg). Patients were assessed for changes in pain intensity using the
modified Severity Symptoms Index and changes in sleep quality using the Pittsburgh Sleep
Quality Index. Results showed that all three groups experienced a reduction in pain symptoms
and an improvement in sleep quality when comparing pretreatment and treatment scores (11).
An open-label dose-titration study investigated the effectiveness and tolerability of
tizanidine hydrochloride tablets in preventing chronic daily headaches. The dosage was
gradually increased from 2 mg at bedtime to a median daily dose of 14 mg (mean 13.5; SD 4.3;
range 4 to 20), divided over three doses per day by the fourth week of treatment. Significant
improvements were observed in overall headache status, mood, sleep, quality of life (P <
.00001), as well as sexual function (P = .0075), and the Beck Depression Inventory-II scores
(P = .00073). Mild-to-moderate adverse events reported by 10% of patients included
somnolence, asthenia, and dry mouth. Three patients discontinued treatment due to somnolence,
dry mouth, or constipation. Additionally, one patient experienced elevated liver enzymes
which normalized after discontinuing the medication (12).
Adverse Effects and Pharmacokinetic Considerations of Tizanidine
Adverse reactions associated with tizanidine include hypotension, bradycardia, or excessive
sedation requiring gradual dose reduction or stopping therapy (9). Given its extensive
hepatic metabolism, tizanidine's pharmacokinetics can be significantly altered in patients
with hepatic impairment. Thus, special attention must be given to the dosing and monitoring
of tizanidine in such individuals to mitigate risks (9). Similarly, patients with renal
impairment, particularly those with a creatinine clearance below 25 mL/min, require careful
management when using tizanidine. Initiation at lower doses, along with close monitoring of
therapeutic response, is recommended (9). Any decision to prescribe tizanidine during
pregnancy should involve a thorough risk-benefit assessment to ensure the safety of both the
mother and the fetus. Moreover, considering tizanidine's lipid-soluble nature, potential
transfer into breast milk raises concerns regarding its use during lactation (9). Smoking has
been identified as a factor that reduces tizanidine's plasma concentration and exposure, as
observed in studies such as Al-Ghazawi et al. (13)
Following oral administration of tizanidine, the peak plasma concentrations occurred 1 hour
after with a half-life of approximately 2 hours. (14). The doses employed in the present
study constitute an initial dose of 2 mg HS, and it will be titrated up by 2 mg every 4 days,
as per response and tolerability, up to a maximum dose of 0.1 mg/kg/HS administered before
bedtime. This proposed dose was found effective in a clinical trial assessing the effects of
tizanidine for refractory sleep disturbance in disabled children with spastic quadriplegia.
The clinical trial included 21 children diagnosed with spastic quadriplegia and experiencing
severe sleep disturbances. All these children exhibited abnormalities in both falling asleep
and staying asleep. Tizanidine was administered at a dosage ranging from 0.1 to 0.2
mg/kg/day, divided into two or three doses. If daytime drowsiness was significant, tizanidine
administration was limited to just before bedtime. Improvement in sleep induction and/or
maintenance was observed in 13 patients (61.9%). Moreover, the families of the patients
expressed satisfaction with the treatment (15).
The objective of this study was to compare in a double-blind design the subjective hypnotic
efficacy and safety of Tizanidine (0.1 mg/kg/day), and a Zolpidem 10 mg HS over 12 weeks in
adult patients with primary insomnia.
Study Objectives
Primary Objective:
To evaluate the efficacy of Tizanidine compared to Zolpidem in improving sleep quality among
patients with primary insomnia.
Secondary Objectives:
- To assess the safety and side effect profile of Tizanidine.
- To compare patient tolerance and satisfaction between Tizanidine and Zolpidem
treatments.
Hypotheses
Main Hypothesis:
Tizanidine is effective in the treatment of primary insomnia, offering a better safety
profile with fewer side effects.
Secondary Hypotheses:
- Patients treated with Tizanidine will report fewer side effects compared to those
treated with Zolpidem.
- Tizanidine will demonstrate higher patient tolerance and satisfaction in the treatment
of primary insomnia.
Methodology
Study Design:
This study will be conducted as a double-blind, randomized controlled trial. Participants
will be randomly assigned to receive either Tizanidine or Zolpidem for 12 weeks.
The trial design is a parallel-group randomized controlled trial. Participants will be
randomly assigned to either one of the two treatment groups: the Tizanidine group or the
Zolpidem group. This design allows for the comparison of the efficacy and safety of
Tizanidine versus Zolpidem in the treatment of primary insomnia. The allocation ratio will be
1:1, ensuring an equal distribution of participants between the two treatment arms.
Trial setting:
The data were collected at the outpatient sleep clinic affiliated with Al-Masarah Hospital,
Muscat, Oman.
Randomization:
The method used to generate the random allocation sequence:
The random allocation sequence was generated using a computerized random number generator.
The type of randomization:
Simple randomization was employed, where each participant had an equal chance of being
assigned to either the tizanidine group or the Zolpidem group.
Study procedures:
Study medications:
- Tizanidine Group:
- At all evenings and mornings during the treatment period at home, participants will
be asked to document the sleep diaries and to wear the actigraphy. Sleep diaries
are collected by the research assistant every week.
- Every 4 weeks the patients will be asked to complete the questionnaires (Pittsburgh
Sleep Quality Index (PSQI), and another self-report of suspected adverse drug
reaction form).
- At baseline, then in the 6th week, and 12th week of the treatment, the participants
will be asked to attend the OPD for a clinical assessment by a specialist
psychiatrist researcher. The Clinical Global Impression (CGI) scale (severity of
illness, global improvement, and efficacy index) assessed by the researcher
- Throughout the study, compliance was monitored by the research assistant calling
the patients every other day in the morning.
- Safety was assessed by adverse events (spontaneously reported by participants to
the research assistant and/or assessed/observed by the researcher during the
clinical follow-up visit in 6th week, and 12th week of the study) and vital signs
(heart rate and blood pressure) at baseline, in 6th week, and 12th week of the
treatment.
- Polysomnography (PSG) at baseline and within one week of the end of the trial will
be carried out.
- At the end of the study period, a medical checkup by a medical officer will be
carried out. In the medical check-up, a medical history will be carried out, a
physical examination (including ECG) and laboratory evaluation will be performed
within 1 week of the end of the study treatment.
- Zolpidem Group:
- At all evenings and mornings during the treatment period at home, participants will
be asked to document the sleep diaries and to wear the actigraphy.
- Every 4 weeks the patients will be asked to complete the questionnaires (Pittsburgh
Sleep Quality Index (PSQI), and another self-report of suspected adverse drug
reaction form).
- At baseline, then in the 6th week, and 12th week of the treatment, the participants
will be asked to attend the OPD for a clinical assessment by a specialist
psychiatrist researcher. The Clinical Global Impression (CGI) scale (severity of
illness, global improvement, and efficacy index) assessed by the researcher
- Throughout the study, compliance was monitored by the research assistant calling
the patients every other day in the morning.
- Safety was assessed by adverse events (spontaneously reported by participants to
the research assistant and/or assessed/observed by the researcher during the
clinical follow-up visit in 6th week, and 12th week of the study) and vital signs
(heart rate and blood pressure) at baseline, in 6th week, and 12th week of the
treatment.
- Polysomnography (PSG) at baseline and within one week of the end of the trial will
be carried out.
- At the end of the study period, a medical checkup by a medical officer will be
carried out. In the medical check-up, a medical history will be carried out, a
physical examination (including ECG) and laboratory evaluation will be performed
within 1 week of the end of the study treatment.
- Administration: Both medications will be administered orally, 30 minutes before bedtime.
Outcome Measures:
1. - Primary Outcome: Improvement in sleep quality, measured using the Pittsburgh Sleep
Quality Index (PSQI).
2. - Secondary Outcomes: Frequency and severity of side effects, and patient satisfaction
(assessed through a self-report of suspected adverse drug reaction form).
Data Collection Methods:
- Sleep diaries and actigraphy will be used to collect data on sleep patterns every
morning, and every night.
- Standardized questionnaires at the 4th week, 8th week, and 12th week of the study
include the Pittsburgh Sleep Quality Index (PSQI), and a self-report of suspected
adverse drug reaction form.
- Clinical follow-up visits during the 4th week of intervention, 8th week of intervention,
and the 12th week of intervention will be scheduled to monitor progress and gather
subjective assessments.
- Polysomnography (PSG) at baseline and within one week of the end of the trial will be
carried out.
Actigraphy
This is a method used to monitor activity and sleep-wake patterns over the study period. It
involves wearing a small, wrist-worn device called an actigraph, which contains sensors that
detect movement and record activity levels continuously.
Sleep diaries
These are self-reported records in which participants will be asked to track various aspects
of their sleep-wake patterns over the study period. individuals are typically asked to fill
out sleep diaries first thing in the morning, immediately upon waking up. The diaries will
involve recording information about bedtime, wake-up time, sleep onset latency (time taken to
fall asleep), wake after sleep onset (time spent awake during the sleep period), and any
nighttime awakenings.
Polysomnography (PSG)
Polysomnography, a diagnostic examination employed during sleep, gathers physiological data
through various sensors including electroencephalogram (EEG), electrooculogram (EOG),
electromyogram (EMG), electrocardiogram (ECG), pulse oximetry, airflow, and respiratory
effort.
Pittsburgh Sleep Quality Index (PSQI)
The Pittsburgh Sleep Quality Index (PSQI) is a self-administered questionnaire designed to
evaluate sleep quality within one month. It comprises 19 specific items organized into seven
components, ultimately generating a single global score. It is a widely used and validated
instrument for assessing sleep quality in research and clinical settings. It has been
extensively validated in various populations and has demonstrated good psychometric
properties (17), including reliability and validity in the Arabic version (18). This scale is
copyrighted and is owned by the University of Pittsburgh and may be reprinted & used without
charge only for non-commercial research and educational purposes.
Clinical Global Impression
Self-report of suspected adverse drug reaction form
Patients will be asked to fill out a pre-determined suspected adverse drug reaction form once
a side-effect is suspected. Moreover, the research assistant will be utilizing a suspected
side-effect form and will be conducting an interview another day to assess the patient for
any suspected side-effects.
Sample size
The sample size was estimated based on the anticipated difference (effect size) in the
primary outcome between the two treatments (Tizanidine Vs Zolpidem) for the primary insomnia
patients. The primary outcome considered was the mean global PSQI score before and after the
treatment. We anticipated a medium effect size (Cohen's f = 0.25, Repeated measures ANOVA)
for the primary outcome. The type I error alpha was set at 5%, and the power was set at 80%.
The primary outcome will be measured four times (baseline, 4 weeks, 8 weeks, and 12 weeks),
and the anticipated correlation among repeated outcome measures was 0.5. We also considered
an attrition rate (dropout/lost follow up) of 10%. Therefore, the final sample size became 90
subjects (45 in each group). The calculation was done in G*Power version 3.1.9.7.
Data Analysis
Continuous variables will be presented as mean, median, standard deviation, and interquartile
range, whereas categorical variables will be presented as frequency and percentage.
Comparison of mean scores between two independent groups will be assessed using the
independent samples t-test, whereas comparison of paired mean scores within the groups will
be assessed using the paired samples t-test. A repeated measures ANOVA will be applied to
evaluate the changes over time in the sleep quality between the two treatment groups.
Association between two categorical variables will be assessed using a Chi-square test
(Fisher's exact/Likelihood ratio). A P-value less than 0.05 will be considered statistically
significant. All the analysis will be carried out in IBM SPSS Statistics (IBM Corp. Released
2022. IBM SPSS Statistics for Windows, Version 29.0. Armonk, NY: IBM Corp).
Ethical Considerations
Informed Consent:
In the informed consent process, all potential participants will receive detailed information
about the study. A designated researcher from the study team will verbally explain the study
in a language that is understandable to the participants. This discussion will take place in
the outpatient sleep clinic and will be witnessed by another researcher to ensure
transparency and accuracy. Any questions or concerns raised by the participants will be
addressed at this time. Suppose the participant agrees to participate in the study. In that
case, they will be provided with a comprehensive information and consent sheet outlining the
study's purpose, procedures, potential risks and benefits, confidentiality measures, and
their rights as participants. Subsequently, the participant will be asked to sign the consent
form. Both the researcher who explained the study and the witnessing researcher will also
sign the form to acknowledge the participant's informed consent.
Confidentiality:
All data collected throughout the study will be anonymized to remove any personally
identifiable information. Additionally, measures will be implemented to ensure the secure
storage of data. Access to study information will be restricted to authorized research
personnel only, and data will be stored on a password-protected computer.
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