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The researcher and principal investigator working on this study left the institution.
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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
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:
Exclude:
Response Variables:
Explanatory Variables:
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]
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Bilateral Carpal Tunnel Syndrome (CTS) |
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| Measure | Description | Time Frame |
|---|---|---|
| Overall Pain Intensity | 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. | 2 weeks after surgery within 6 month timeframe |
| Measure | Description | Time Frame |
|---|---|---|
| Overall Satisfaction | 11-point ordinal measure of satisfaction with treatment measured 2 weeks after surgery during suture removal | 2 weeks after surgery within a 6 month timeframe |
| Patient Reported Outcome for Upper Extremity Function |
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Inclusion Criteria:
Exclusion Criteria:
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Bilateral CTS patients undergoing bilateral carpal tunnel release
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | United States |
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| ID | Term |
|---|---|
| D002349 | Carpal Tunnel Syndrome |
| D010146 | Pain |
| ID | Term |
|---|---|
| D020423 | Median Neuropathy |
| D020422 | Mononeuropathies |
| D010523 | Peripheral Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
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PROMIS upper extremity
| 2 weeks after surgery within 6 month timeframe |
| Electromyogram Results | EMG DSL and DML | Before Surgery |
| Demographics | Age, sex, race, occupation, avocation | 2 weeks after first surgery |
| Comorbidities | Relevant comorbidities: TMC Arthrosis, ulnar neuropathy, trigger finger | 2 weeks after surgery |
| Hand Dominance and Side of Surgery | 2 weeks after surgery |
| Patient Reported Pain Interference | PROMIS Pain Interference (CAT) | 2 weeks after surgery within 6 month timeframe |
| Patient Self Efficacy Questionnaire | PSEQ-2 | 2 weeks after surgery within 6 month timeframe |
| Patient Reported Depression | PROMIS Depression | 2 weeks after surgery within 6 month timeframe |
| D009422 | Nervous System Diseases |
| D009408 | Nerve Compression Syndromes |
| D012090 | Cumulative Trauma Disorders |
| D013180 | Sprains and Strains |
| D014947 | Wounds and Injuries |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |