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Consecutive Series Outcomes Review of Patients Undergoing a New Single Portal Technique for Endoscopic Carpal Tunnel Release

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified April 2013 by Rothman Institute Orthopaedics.
Recruitment status was:  Active, not recruiting
Sponsor:
Information provided by:
Rothman Institute Orthopaedics
ClinicalTrials.gov Identifier:
NCT00968123
First received: August 27, 2009
Last updated: April 8, 2013
Last verified: April 2013
  Purpose

The Purpose of this study is to report a new single portal endoscopic release technique and the sequence of the first 50 patients who underwent this release.

This will be a chart review of the demographics, outcomes, and complications of a sequential series of patients undergoing a Seg-Way Endoscopic carpal tunnel release (ECTR).


Condition
Carpal Tunnel

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: Consecutive Series Outcomes Review of Patients Undergoing a New Single Portal Technique for Endoscopic Carpal Tunnel Release

Resource links provided by NLM:


Further study details as provided by Rothman Institute Orthopaedics:

Primary Outcome Measures:
  • Functional outcomes following carpal tunnel release

Secondary Outcome Measures:
  • Complications and return to work data will also be reviewed

  Eligibility

Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Sampling Method:   Probability Sample
Study Population
This is a consecutive series, retrospective review of the first 50 patients who have undergone carpal tunnel release surgery using a new single portal endocopic technique.
Criteria

Inclusion Criteria:

  • This will be a chart review of the first 50 patients who have had surgery using the single portal technique
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00968123

Locations
United States, Pennsylvania
Rothman Institute
Philadelphia, Pennsylvania, United States, 19107
Sponsors and Collaborators
Rothman Institute Orthopaedics
  More Information

Responsible Party: Charles Leinberry, MD, Rothman Institute
ClinicalTrials.gov Identifier: NCT00968123     History of Changes
Other Study ID Numbers: RIUCLEI 09-02
Study First Received: August 27, 2009
Last Updated: April 8, 2013

Additional relevant MeSH terms:
Carpal Tunnel Syndrome
Median Neuropathy
Mononeuropathies
Peripheral Nervous System Diseases
Neuromuscular Diseases
Nervous System Diseases
Nerve Compression Syndromes
Cumulative Trauma Disorders
Sprains and Strains
Wounds and Injuries

ClinicalTrials.gov processed this record on September 20, 2017