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临床试验/NCT02198521
NCT02198521撤回不适用

Staged Bilateral Carpal Tunnel Release: Which Side Hurts More?

Massachusetts General Hospital1 个研究点 分布在 1 个国家开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Overall Pain Intensity

研究概览

简要总结

Title Staged Bilateral Carpal Tunnel Release: Which Side Hurts More? Primary null hypothesis Patients undergoing staged bilateral open Carpal Tunnel Release (CTR) have no difference in overall pain intensity of pain between sides.

Secondary null hypotheses

  • There is no correlation in overall pain intensity after open CTR surgery and distal sensory latency, distal motor latency, electromyography (EMG), demographics, occupation, avocation, relevant comorbidities, dominance, left vs. right, Pain Self-Efficacy, Patient Reported Outcomes Measurement Information System (PROMIS) Upper Extremity or PROMIS depression when both surgeries are performed within 6 months.
  • There is no difference in satisfaction with treatment at the time of suture removal after the first and second open CTR surgery when both are performed within 6 months..

IRB: 2009-p-001-019 ClinicalTrials.gov: Not mandatory, (b/o observational) Authors: Drijkoningen, Braun, Ring Journal: To be discussed Design: Prospective cohort study Background Many hand surgeons note that patients undergoing staged bilateral open carpal tunnel release often experience more pain with the second side. The investigator felt this was an easily testable hypothesis worthy of study.

Subjects

Eligibility:

Inclusion:

  • Age 18 or older
  • Idiopathic carpal tunnel syndrome
  • No prior surgery for carpal tunnel syndrome

Exclude:

  • Pregnant women
  • Not fluent in English

Response Variables:

  • 11-point ordinal measure of overall pain intensity during and after surgery measured at the time of suture removal.
  • 11-point ordinal measure of satisfaction with treatment
  • PROMIS upper extremity

Explanatory Variables:

  • Distal Sensory Latency (DSL)
  • Distal Motor Latency (DML)
  • EMG changes
  • Demographics: age, sex, race, occupation, avocation
  • Time limit between two surgeries < 6 months
  • Relevant comorbidities: Trapeziometacarpal (TMC) arthrosis, ulnar neuropathy, trigger finger
  • Involved hand (Dominance, Side)
  • First side vs. second side surgery
  • PROMIS Pain Interference Computer Adaptive Testing (CAT)
  • Pain Self Efficacy Questionnaire (PSEQ-2)
  • PROMIS Depression

Methods The investigator and study staff will invite all adult patients (age 18 and older) presenting to the Orthopaedic Hand and Upper Extremity Service Department at Massachusetts General Hospital (MGH) with bilateral carpal tunnel syndrome planning staged bilateral carpal tunnel release.

Analysis Power analysis An a priori power analysis for matched pairs was performed. To detect the difference between two dependent means an effect size of 0.5 at alpha of 0.05 and 80% power, a total sample size of 34 patients is needed.As the investigator expects to have patients who will be lost to follow-up the investigators will count 10% extra, a total of 38 patients will be needed.

Univariate analysis: Variables will be presented with frequencies and percentages for categorical variables and as mean with standard deviation or median with interquartile range for respectively normal or non-normal distributed continuous variables. Normality of continuous distributed variables will be tested a paired T-Test.

Bivariate and multivariable analysis will be performed and subsequently all variables with a probability < 0.10 in bivariate analysis will be inserted in a backward, stepwise, multivariable linear regression analysis to assess their ability to explain variation in outcome. The 11 point Likert Pain scale score is considered significant when there is a difference of more than 1.4 points (2.8 SD*0.5 effect size)on a scale from 1-10.[9]

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or older
  • Idiopathic carpal tunnel syndrome
  • No prior surgery for carpal tunnel syndrome

排除标准

  • Pregnant women
  • Not fluent in English

结局指标

主要结局

Overall Pain Intensity

时间窗: 2 weeks after surgery within 6 month timeframe

The overall pain intensity is measured on an 11-point ordinal measure of overall pain intensity after surgery measured at the time of suture removal.

次要结局

  • Electromyogram Results(Before Surgery)
  • Overall Satisfaction(2 weeks after surgery within a 6 month timeframe)
  • Patient Reported Outcome for Upper Extremity Function(2 weeks after surgery within 6 month timeframe)
  • Hand Dominance and Side of Surgery(2 weeks after surgery)
  • Patient Reported Pain Interference(2 weeks after surgery within 6 month timeframe)
  • Demographics(2 weeks after first surgery)
  • Comorbidities(2 weeks after surgery)
  • Patient Self Efficacy Questionnaire(2 weeks after surgery within 6 month timeframe)
  • Patient Reported Depression(2 weeks after surgery within 6 month timeframe)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David C. Ring, MD

MD/PhD

Massachusetts General Hospital

研究点 (1)

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