A Single-portal Endoscopic Approach Through Subcutaneous Tunnel for Carpal Tunnel Release
Primary Purpose
Carpal Tunnel Syndrome
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
a single-portal palm approach
Sponsored by
About this trial
This is an interventional treatment trial for Carpal Tunnel Syndrome focused on measuring Carpal tunnel syndrome, carpal tunnel release, pain, nerve compression syndromes
Eligibility Criteria
Inclusion Criteria:
- A confirmed diagnosis of carpal tunnel syndrome based on Evidence for Surgical Treatment issued by the British Society for Surgery of the Hand
- Symptoms of carpal tunnel syndrome had lasted>2 months or inadequate responses to the non-surgical treatments≥3 months
- moderate to severe symptoms.
Exclusion Criteria:
- mild symptoms or prior injuries to the extremity
- bilateral wrists involved, a combined nerve compression, gout, diabetes or chronic renal failure.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
single-portal group
Arm Description
The patients in single-portal group were treated with single-portal palm approach
Outcomes
Primary Outcome Measures
The sensibility of the pulps of thumb, index finger, and middle finger (mm)
static 2-point discrimination (2PD) test is used for testing the sensibility of the pulps of digits. The range of normal value is 3 mm--5 mm, and higher scores mean a worse outcome
Severity of symptoms and functional status
The Levine Questionnaire is regarded as a valuable assessment of severity of symptoms and functional status in carpal tunnel syndrome. It is self-administered and is in two sections. The symptoms severity scale is 11 questions and evaluates symptoms regarding severity, frequency, time and kind. The functional status scale is eight questions and evaluates how the syndrome affects daily life.Each question had five ordinal response categories ranging from 1 (no symptoms) to 5 (very severe symptoms). Responses to individual items were averaged to yield an overall score for each scale.
Secondary Outcome Measures
Full Information
NCT ID
NCT05094778
First Posted
October 2, 2021
Last Updated
October 15, 2021
Sponsor
Shenzhen People's Hospital
Collaborators
Hebei Medical University Third Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05094778
Brief Title
A Single-portal Endoscopic Approach Through Subcutaneous Tunnel for Carpal Tunnel Release
Official Title
A Single-portal Endoscopic Approach Through Subcutaneous Tunnel for Carpal Tunnel Release
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
January 5, 2012 (Actual)
Primary Completion Date
June 15, 2021 (Actual)
Study Completion Date
August 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shenzhen People's Hospital
Collaborators
Hebei Medical University Third Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Traditional endoscopic release directly accesses the carpal tunnel and thus carries a higher risk of nerve irritability, even nerve injury. Based on our anatomical study, the investigators developed a new endoscopic technique through a single-portal palm approach that passes superficially to palmar aponeurosis, and cut the full transverse carpal ligament. The investigators will compared the technique with the standard dual-portal endoscopic technique.
Detailed Description
Conduct a multi-center, comparison clinical trial according to clinical Trial Reporting Standards (CONSORT). Patients in the single-portal group were treated with a single-portal palm approach that passes superficially to palmar aponeurosis and cut the full transverse carpal ligament. The comparison group were treated with Chow endoscopic technique. In order to assess efficiency of single-portal palm approach, the investigators will compared the technique with the standard dual-portal endoscopic technique. The study was approved by Shenzhen People's Hospital and informed consent was signed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carpal Tunnel Syndrome
Keywords
Carpal tunnel syndrome, carpal tunnel release, pain, nerve compression syndromes
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
192 (Actual)
8. Arms, Groups, and Interventions
Arm Title
single-portal group
Arm Type
Other
Arm Description
The patients in single-portal group were treated with single-portal palm approach
Intervention Type
Procedure
Intervention Name(s)
a single-portal palm approach
Intervention Description
a single-portal palm approach that passes superficially to palmar aponeurosis, and cut the full transverse carpal ligament.
Primary Outcome Measure Information:
Title
The sensibility of the pulps of thumb, index finger, and middle finger (mm)
Description
static 2-point discrimination (2PD) test is used for testing the sensibility of the pulps of digits. The range of normal value is 3 mm--5 mm, and higher scores mean a worse outcome
Time Frame
3 years
Title
Severity of symptoms and functional status
Description
The Levine Questionnaire is regarded as a valuable assessment of severity of symptoms and functional status in carpal tunnel syndrome. It is self-administered and is in two sections. The symptoms severity scale is 11 questions and evaluates symptoms regarding severity, frequency, time and kind. The functional status scale is eight questions and evaluates how the syndrome affects daily life.Each question had five ordinal response categories ranging from 1 (no symptoms) to 5 (very severe symptoms). Responses to individual items were averaged to yield an overall score for each scale.
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
A confirmed diagnosis of carpal tunnel syndrome based on Evidence for Surgical Treatment issued by the British Society for Surgery of the Hand
Symptoms of carpal tunnel syndrome had lasted>2 months or inadequate responses to the non-surgical treatments≥3 months
moderate to severe symptoms.
Exclusion Criteria:
mild symptoms or prior injuries to the extremity
bilateral wrists involved, a combined nerve compression, gout, diabetes or chronic renal failure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yongqing Zhuang
Organizational Affiliation
Shenzhen People's Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
30015499
Citation
Shi Q, Bobos P, Lalone EA, Warren L, MacDermid JC. Comparison of the Short-Term and Long-Term Effects of Surgery and Nonsurgical Intervention in Treating Carpal Tunnel Syndrome: A Systematic Review and Meta-Analysis. Hand (N Y). 2020 Jan;15(1):13-22. doi: 10.1177/1558944718787892. Epub 2018 Jul 17.
Results Reference
result
Learn more about this trial
A Single-portal Endoscopic Approach Through Subcutaneous Tunnel for Carpal Tunnel Release
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