Ketamine and Midazolam Infusions for CRPS: Feasibility Study

Complex Regional Pain Syndromes Clinical Trial

Official title:

Feasibility Study Comparing a Ketamine and Midazolam Infusion to a Midazolam-Only Infusion for Complex Regional Pain Syndrome

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT05945147
• Other study ID #: 66661
• Status: Withdrawn
• Phase: Phase 2
• Start date: January 1, 2024
• Est. completion date: May 31, 2024

Study information

• Verified date: February 2024
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will assess the feasibility of administering ketamine plus midazolam or midazolam alone, when infused over 5 days in an outpatient setting, to adults with complex regional pain syndrome (CRPS).

Description:

Subanesthetic ketamine infusions are a potentially impactful treatment for chronic refractory pain, but the acute psychoactive effects of ketamine complicate successful masking in randomized trials. Multi-day ketamine infusions have produced long-lasting, but not permanent, remission of symptoms in complex regional pain syndrome (CRPS), a chronic and often debilitating neuropathic pain condition that can affect one or more limbs. In this feasibility study, 4 adults with CRPS will be randomized to receive either ketamine and midazolam or midazolam-only, infused over 5 days in an outpatient setting. The objectives of this feasibility study are: 1. Assess whether the recruitment and retention rate observed in this feasibility study can support a larger clinical trial. 2. Evaluate whether participants can adhere to study procedures. 3. Determine whether midazolam, when given alone as an intravenous (IV) infusion, can be used as an active placebo that is well-tolerated, practical, and believable compared to a ketamine plus midazolam infusion. 4. Gather preliminary data on clinically-relevant outcomes for CRPS.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: May 31, 2024
• Est. primary completion date: April 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

• Age 18 to 65 years
• Meets the International Association for the Study of Pain (IASP) diagnostic criteria for complex regional pain syndrome (CRPS)
• Primary complaint of CRPS-attributable pain for =3 months
• Average pain intensity of =3/10 over the last month
• Can read and comprehend English-language questionnaires
• Can receive text messages by phone
• Can identify a responsible adult who can provide transportation to and from infusion site for 5 consecutive days (Mon-Fri)

Related Conditions & MeSH terms

• Complex Regional Pain Syndromes
• Reflex Sympathetic Dystrophy
• Syndrome

Intervention

Drug:
• Ketamine
An escalating dose of ketamine (0.15 to 0.4 mg/kg/hr) will be administered as 4-hour infusions over 5 consecutive days
• Midazolam
A constant dose of midazolam (0.04 mg/kg/hr) will be administered as 4-hour infusions over 5 consecutive days
• Normal Saline
An escalating dose of normal saline (0.15 to 0.4 mg/kg/hr) will be administered as 4-hour infusions over 5 consecutive days

Locations

Country	Name	City	State
United States	Stanford University	Stanford	California

Sponsors (1)

Lead Sponsor	Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number and proportion of patients who can undergo the steps of recruitment, informed consent, enrollment, and randomization	Out of all patients identified as potentially eligible for the study based on chart review, we will measure the number and proportion who can undergo the steps of recruitment, informed consent, enrollment, and randomization during a 2-month period.	2 months after the study opens for enrollment
Primary	Number and proportion of randomized participants who remain in the study until the last follow-up timepoint	Out of all patients who were randomized to a treatment group, we will measure the number and proportion who remain in the study until their last follow-up timepoint.	8 weeks after receiving intervention
Primary	Change in participant masking	Participants will be asked to guess their assigned treatment in a forced binary choice and to rate their level of confidence on a scale from 0 to 100%.	Daily during intervention administration (5 days), and once at 8 weeks after receiving intervention
Primary	Change in participant masking	Participants will be asked to guess their assigned treatment in a forced binary choice and to rate their level of confidence on a scale from 0 to 100%.	During intervention administration
Primary	Change in investigator masking	Investigators administering and monitoring the drug infusions will be asked to guess the participant's assigned treatment in a forced binary choice and to rate their level of confidence on a scale from 0 to 100%.	8 weeks after receiving intervention
Primary	Change in investigator masking	Investigators administering and monitoring the drug infusions will be asked to guess the participant's assigned treatment in a forced binary choice and to rate their level of confidence on a scale from 0 to 100%.	During intervention administration
Primary	Number and types of adverse events	Adverse events will be elicited from the participant in a brief, open-ended structured interview.	8 weeks after receiving intervention
Secondary	Pain intensity	A numerical rating scale ranging from 0 (no pain) to 10 (worst pain imaginable) over the past 24 hours will be used to assess pain intensity.	Baseline, daily during treatment (5 days), and daily for 8 weeks after treatment
Secondary	Treatment expectancies	The 6-item Healing Encounters and Attitudes Lists (HEAL) Short Form for Treatment Expectancy will be used to assess self-reported expectations about the study treatment. Participants are asked to rate their agreement with brief statements such as, "This treatment will be successful" and "I am confident in this treatment".	Baseline, and daily during treatment (5 days)
Secondary	Pain interference	The 6-item PROMIS Pain Interference Short Form assesses the extent to which pain hinders engagement with social, cognitive, emotional, physical, and recreational activities. Items are self-rated on a 5-point scale ranging from 1 ("Not at all") to 5 ("Very Much"). Raw score totals are converted to standardized T-scores, with a higher T-score representing greater pain interference.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Physical function	The 6-item PROMIS Physical Function Short Form assesses the ability to carry out physical tasks and activities in one's daily life. Items are self-rated on a 5-point scale ranging from 1 ("Unable to do") to 5 ("Without any difficulty"). Raw score totals are converted to standardized T-scores, with a higher T-score representing better physical function.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Depression (PROMIS)	The 6-item PROMIS Depression Short Form assesses the severity of depressive symptoms experienced by an individual. Items are self-rated on a 5-point scale ranging from 1 ("Never") to 5 ("Always"). Raw score totals are converted to standardized T-scores, with a higher T-score representing greater depression symptom severity.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Depression (PHQ-9)	The 9-item PHQ-9 will be used as an additional indicator for changes in depression symptom severity, and to monitor for any risk of acute suicidality during the trial (item #9: "Thoughts that you would be better off dead, or of hurting yourself"). Items are self-rated on a 4-point scale ranging from 0 ("Not at all") to 3 ("Nearly every day"). Higher total scores indicate greater depression symptom severity.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Anxiety	The 6-item PROMIS Anxiety Short Form assesses the severity of anxiety symptoms experienced by an individual. Items are self-rated on a 5-point scale ranging from 1 ("Never") to 5 ("Always"). Raw score totals are converted to standardized T-scores, with a higher T-score representing greater anxiety symptom severity.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Sleep disturbance	The 6-item PROMIS Sleep Disturbance Short Form assesses the severity of sleep-related issues, such as trouble falling asleep, staying asleep, and experiencing non-restorative sleep. Items are self-rated on a 5-point scale ranging from 1 ("Not at all") to 5 ("Very Much"). Raw score totals are converted to standardized T-scores, with a higher T-score representing greater sleep disturbance.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Pain catastrophizing	The 13-item Pain Catastrophizing Scale assesses the extent to which an individual engages in magnifying, rumination, and helplessness thoughts related to their pain experience. Items are self-rated on a 5-point scale ranging from 0 ("Not at all") to 4 ("All the time"). Higher total scores indicates higher levels of pain catastrophizing.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Chronic pain acceptance	The 8-item Chronic Pain Acceptance Questionnaire assesses one's level of acceptance and willingness to engage in valued activities despite the presence of chronic pain. Items are self-rated on a 7-point scale ranging from 0 ("Never true") to 6 ("Always true"). Higher total scores indicate greater levels of chronic pain acceptance.	Baseline, and weekly for 8 weeks after the end of treatment
Secondary	Patient global impression of change	The Patient Global Impression of Change scale assesses the patient's perception of change in their overall health status resulting from a specific treatment. The single-item scale is self-rated on a 7-point scale ranging from 1 ("Very much improved") to 7 ("Very much worse").	Weekly for 8 weeks after the end of treatment
Secondary	Number of painful body regions	The CHOIR Body Map is a visual tool that allows individuals to indicate the location(s) of their pain on a human body outline.	Baseline, and weekly for 8 weeks after the end of treatment