Mechanisms of Sleep Disruption Hyperalgesia

Pain Clinical Trial

— ESP2  

Official title:

Mechanisms of Sleep Disruption Hyperalgesia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01794689
• Other study ID #: NA_00071465
• Secondary ID: 1R01DA032922-01
• Status: Completed
• Phase: N/A
• Start date: May 2013
• Est. completion date: March 12, 2019

Study information

• Verified date: August 2019
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Twenty percent of Americans suffer from chronic pain. Sleep disturbance is similarly prevalent and among the most common and disabling neurobehavioral problems associated with chronic pain. This research is designed to evaluate the effects of disrupted sleep patterns on mood, inflammation, the perception of pain, and pain relief. This study will help researchers understand the relationship between sleep and pain, and how sleep disturbance might influence chronic pain conditions.

Description:

This research is being conducted in order to evaluate the effects of disrupted sleep patterns on mood, inflammation, the perception of pain, and pain relief. This study will help researchers understand the relationship between sleep and pain, and how sleep disturbance might influence chronic pain conditions. Healthy participants will undergo baseline sleep and sleep disruption conditions. Following undisturbed sleep and sleep disruption conditions, sensitivity to pain and analgesic response (via morphine or placebo administration) will be assessed using a heat-capsaicin pain model.

This study will be conducted in 2 major parts—3 screening visits (2 outpatient and 1 inpatient) and 2 experimental inpatient visits. Part 1 of the study will involve a 1-week screening period. This will involve two separate screening visits lasting about 2 hours each. At Screening Visit 1, participants will complete questionnaires, an interview, and undergo toxicology screening. At Screening Visit 2, participants will complete questionnaires, undergo a physical exam, and be familiarized with pain testing procedures. At Screening Visit 3, participants will undergo an inpatient sleep study.

Part 2 will involve two different inpatient admissions. The two admissions will be separated by at least two weeks. During each of the admissions, participants' sleep will be studied at night. The first admission will begin immediately following the overnight sleep study in Screening Visit 3. One of the admissions will be for one night and the other admission will be for three nights. For the one night admission, participants will sleep undisturbed for an 8-hour period. For the three night admission, participants will undergo sleep disruption for two nights in a row. On the third night, participants will be allowed to sleep undisturbed for 8 hours for recovery.

During both inpatient admissions, pain testing procedures will be completed that will last approximately 5 hours during the day. During testing, small amounts of blood will be drawn for analysis. Participants will be randomly assigned to two groups. Group A will be given a standard dose of morphine during pain testing. Group B will be given a placebo during pain testing.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: March 12, 2019
• Est. primary completion date: January 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 48 Years

Eligibility

Inclusion Criteria:

• Healthy

• Age 18-48

• Meets Research Diagnostic Criteria for Normal Sleepers

• Stable sleep phase within 21:00 and 08:00

• Total sleep time between 6.5 and 8.5 hours per night

• Sleep efficiency =85%

• Epworth Sleepiness Scale Score <10

• Non-smoker/non-nicotine users

• Low Caffeine Users (=2 cups per day)

Exclusion Criteria:

• Body Mass Index =35

• Lifetime history of chronic pain (>6 months)

• Acute pain

• Significant medical or psychiatric morbidity within 6 months

• Lifetime history of bipolar disorder, psychotic disorder, serious recurrent major depression, serious post-traumatic stress disorder, or seizure disorder

• Respiratory, hepatic, renal, or cardiac conditions that would contraindicate opioid use

• Lifetime history of alcohol or substance abuse or dependence

• Lifetime history of opioid use >36 doses or >7 days of consecutive use

• Prior adverse reaction to general anesthetics, opioids, or capsaicin

• Clinically significant abnormal complete blood count or comprehensive metabolic profile

• Positive toxicology screen for opioids or recreational drugs

• Pregnant or lactating women

• Significant pre-admission psychological distress (T-scores >64 on the Brief Symptom Inventory Global Scales)

• Significant lifetime history of serious head injury that is determined to influence pain processing or sleep systems

Related Conditions & MeSH terms

• Hyperalgesia
• Pain
• Sleep Deprivation

Intervention

Drug:
• Morphine
0.08mg/kg will be administered to participants randomly assigned to receive the drug via IV bolus during each quantitative sensory testing session (after one night of uninterrupted sleep and after 2 nights of forced awakenings).
• Saline Placebo
Saline Placebo will administered to participants randomly assigned to receive the placebo via IV bolus during each quantitative sensory testing session (after one night of uninterrupted sleep and after 2 nights of forced awakenings).

Behavioral:
• Forced Awakenings
Participants will be awakened each hour during an 8 hour sleep opportunity period. One of the awakenings is for 60 minutes and randomly determined. The other 7 awakenings are for 20 minutes each, and are randomly scheduled to occur in either the first second or third tertile of each hour. The maximum total sleep time a participant will receive is 280 minutes.
• Uninterrupted Sleep
Participants will receive an 8 hour period of undisturbed sleep

Locations

Country	Name	City	State
United States	Johns Hopkins University Bayview Medical Center	Baltimore	Maryland

Sponsors (2)

Lead Sponsor	Collaborator
Johns Hopkins University	National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Total Sleep Time	The degree of sleep deprivation will be assessed by total sleep time (TST) in minutes during the uninterrupted sleep condition compared to the forced awakenings conditions.	Next day during quantitative sensory testing after 2 nights of forced awakenings or uninterrupted sleep.
Primary	Spinal Sensitization as Assessed by Area of Secondary Hyperalgesia (2HA) After Two Nights of Uninterrupted Sleep and Two Nights of 8 Forced Awakenings	The area of secondary hyperalgesia (2HA) to mechanical stimulation was quantified by stimulating along eight linear paths near the capsaicin treated site using a 15 gram nonpainful von Frey filament. Stimulation occurred until the participant reported a change in sensation from which a border was marked on the skin. The degree of 2HA was assessed by measuring the total surface area (mm^2) of the marked borders. Data were collapsed by group to analyze the effects of FA vs US, irrespective of randomization group. Our Primary Secondary Hyperalgesia outcome was measured prior to injection of either morphine or placebo.	Next day during quantitative sensory testing after 2 nights of forced awakenings or uninterrupted sleep
Secondary	Opioid Analgesia as Assessed by Analgesia Index (Seconds)	After 2 nights of forced awakenings and after two nights of uninterrupted sleep, opioid analgesia will be assessed by an analgesia index. The analgesia index is calculated using withdrawal latency during cold pressor testing (lasting maximum of 300 seconds). Cold Pressor Testing is done before and after morphine or placebo injection. The difference in withdrawal time before and after morphine or placebo injection is the analgesia index with a minimum score of -300 seconds and maximum score of 300 seconds. These data were log transformed. Mean analgesia index was then calculated for each group. Higher means represent greater analgesia.	Next day after 2 nights of forced awakenings or uninterrupted sleep
Secondary	Mean Change in Percentage of Peripheral Blood Mononuclear Cells Expressing Interleukin-6 After LPS Stimulation	After 2 nights of forced awakenings, and two nights of uninterrupted sleep, blood is drawn (approximately every 60 minutes) during quantitative sensory testing; 4 hours pre-morphine/placebo administration and 2 hours post-morphine/placebo administration to examine markers of inflammation. Two blood samples for each participant are analyzed at 7 separate time points. The marker of inflammation assessed is the number of peripheral blood mononuclear cells expressing Interleukin-6 (IL-6), and the outcome measure represents the mean change in IL-6 levels pre and post stimulation with lipopolysaccharide (LPS). Cellular IL-6 expression was was quantified via flow cytometry.	Next day after 2 nights of forced awakenings or uninterrupted sleep, every 60 minutes up to 7 hours