Effect of Gabapentin and Tizanidine on Insomnia in Chronic Pain Patients: A Randomized, Double-blind, Placebo-controlled Crossover Trial.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 9
- 试验地点
- 1
- 主要终点
- Sleep quality
研究概览
简要总结
This is a double-blind, placebo-controlled, randomized, crossover trial aimed at assessing the effect of gabapentin and tizanidine, two pain medications, on insomnia in chronic pain patients.
详细描述
Chronic pain and insomnia are highly prevalent conditions affecting 10-25% and 6-10% of the general population, respectively. Importantly, these two conditions frequently co-occur, with 50-80% of chronic pain patients reporting sleep disturbances. Identifying medication that alleviates pain and insomnia simultaneously may help reduce risks associated with polypharmacy, including drug-drug interactions.
In this double-blind, placebo-controlled, randomized, crossover trial, gabapentin and tizanidine, two drugs which are respectively commonly used to treat neuropathic and musculoskeletal pain, will be compared to each other and to placebo in their ability to alleviate insomnia in chronic pain patients.
In each week, patients will receive 3-night (Friday-Sunday) trials each of placebo, gabapentin or tizanidine in a randomized, double-blind order and will monitor their insomnia using the Athens Insomnia Scale (AIS) questionnaire (adapted to fit the time frame of this trial). The primary outcome consists of the difference in mean AIS scores between the 3 treatments at the primary time point, which is Monday of each week (after 3 nights of drug intake).
Patients will also monitor their sleepiness, pain relief and overall improvement as secondary variants using the Stanford Sleepiness Scale (SSS), Visual Analog Scale (VAS), and Patient's Global Impression of Change (PGIC) questionnaires respectively.
Scores on the Monday preceding the first treatment will serve as baseline and the period between treatments (i.e. Monday-Thursday nights) will serve as a 4-day washout period between treatments.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
Each participant will have an identification number and randomization of drug sequence allocation will be performed a priori using a random number generator by the study pharmacist. The 3 treatments will be identically encapsulated by the study pharmacist. The study pharmacist will place the drug capsules in identical sealed plastic bags labeled "Treatment 1" through "Treatment 3".
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Any ethnicity
- •Must be able to communicate in English
- •Must have access to email and be able to respond to REDCap questionnaires in English
- •Has a chronic pain condition (≥ 3 months of pain)
- •Reports sleep disturbance and scores ≥ 6 on AIS questionnaire
- •Ability to provide informed consent
排除标准
- •Pregnancy
- •Breastfeeding
- •Has diagnosis of chronic kidney disease
- •Has known QT prolongation >500 msec on prior EKG
- •Inability to complete daily questionnaires
- •Allergy to, or intolerance of, any of tizanidine or gabapentin
- •Shift workers
- •Anticipated travel across multiple time zones (jetlag) during the duration of the trial
- •Circadian misalignment
- •Prior syncope experience and/or fear of blood/needles (if a blood draw is required)
研究组 & 干预措施
Tizanidine 2mg
Friday night: 1 capsule Saturday night: 2 capsules Sunday night: Subject chooses 1-2 capsules
干预措施: Tizanidine (Drug)
Gabapentin 300mg
Friday night: 1 capsule Saturday night: 2 capsules Sunday night: Subject chooses 1-2 capsules
干预措施: Gabapentin (Drug)
Placebo
Friday night: 1 capsule Saturday night: 2 capsules Sunday night: Subject chooses 1-2 capsules
干预措施: Placebo (Drug)
结局指标
主要结局
Sleep quality
时间窗: Monday after 3 nights of drug intake
Comparison of group means for Athens Insomnia Scale scores between the 3 treatment groups placebo, gabapentin and tizanidine. Total Athens Insomnia Scale score ranges from 0 to 24. The higher the score, the more severe the insomnia symptoms experienced by the patient.
次要结局
- Alertness(Monday after 3 nights of drug intake)
- Overall improvement(Monday after 3 nights of drug intake)
- Pain Intensity(Monday after 3 nights of drug intake)
- Categorical assessment of insomnia improvement(Monday after 3 nights of drug intake)
研究者
Nathaniel Schuster
Assistant Profesor
University of California, San Diego
