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Carpal Tunnel SyndromeNCT02198521

Staged Bilateral Carpal Tunnel Release: Which Side Hurts More?

An observational study of Carpal Tunnel Syndrome and Pain, run by Massachusetts General Hospital at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Carpal Tunnel Syndrome, Pain
How many people
0 participants
Where
1 siteUnited States
Study dates
Jul 2014to Sep 2016
How long will I take part?
6 Months
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Bilateral CTS patients undergoing bilateral carpal tunnel release

Who may be able to join

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

Who cannot join

  • Pregnant women
  • Not fluent in English

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Massachusetts General Hospital

    Boston, Massachusetts, 02114

Other trials in United States

About this study

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

Read more
  • 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]

Keywords
Patients undergoing staged bilateral open Carpal Tunnel Release (CTR) have no difference in overall pain intensity of pain between sides.
Medical subject headings
Carpal Tunnel Syndrome, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02198521
Study groupRoleWhat they receive
Bilateral Carpal Tunnel Syndrome (CTS)Not described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: 2 weeks after surgery within 6 month timeframe

Secondary outcomes (9)
  1. Overall Satisfaction

    11-point ordinal measure of satisfaction with treatment measured 2 weeks after surgery during suture removal

    Measured: 2 weeks after surgery within a 6 month timeframe

  2. Patient Reported Outcome for Upper Extremity Function

    PROMIS upper extremity

    Measured: 2 weeks after surgery within 6 month timeframe

  3. Electromyogram Results

    EMG DSL and DML

    Measured: Before Surgery

  4. Demographics

    Age, sex, race, occupation, avocation

    Measured: 2 weeks after first surgery

  5. Comorbidities

    Relevant comorbidities: TMC Arthrosis, ulnar neuropathy, trigger finger

    Measured: 2 weeks after surgery

  6. Hand Dominance and Side of Surgery

    Measured: 2 weeks after surgery

  7. Patient Reported Pain Interference

    PROMIS Pain Interference (CAT)

    Measured: 2 weeks after surgery within 6 month timeframe

  8. Patient Self Efficacy Questionnaire

    PSEQ-2

    Measured: 2 weeks after surgery within 6 month timeframe

  9. Patient Reported Depression

    PROMIS Depression

    Measured: 2 weeks after surgery within 6 month timeframe

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jul 2014 (estimated)
  2. Study startJul 2014
  3. Primary completionSep 2016
  4. Study completionSep 2016

Why it stopped: The researcher and principal investigator working on this study left the institution.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
0 participants (actual)
Target duration
6 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT02198521
Sponsor's protocol ID
2009P001019 AME 339
Status last verified
Feb 2017
First submitted
10 Jun 2014
Last updated
3 Feb 2017
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Carpal Tunnel Syndrome and Pain, run by Massachusetts General Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 3 Feb 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall Pain Intensity (time frame: 2 weeks after surgery within 6 month timeframe). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2017.

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