Correlation Between EPB Entrapment Test and Ultrasound Wrist Findings in Patients With deQuervain's Disease

January 19, 2023 updated by: Vijayaraja Elangovan, Velammal Medical College Hospital and Research Institute

The goal of this observational study is to learn about the correlation between EPB entrapment test and ultrasound wrist findings in patients with deQuervain's disease The main questions it aims to answer are:

  • if correlation exist between EPB entrapment test and ultrasound wrist findings in patients with deQuervain's disease ?
  • if the the correlation aid in deciding management of patients with deQuervain's disease Participants will be subjected to
  • EPB entrapment test
  • ultrasound examination of wrist

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

39

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • India
    • Tamil Nadu
      • Madurai, Tamil Nadu, India, 625009
        • Velammal medical college hospital and research institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

all adults >18 years of age with positive Finkelsteins test are included

Description

Inclusion Criteria:

  • Age >18
  • Radial side wrist pain
  • Finkelstein test positive
  • Failure of non surgical treatment

Exclusion Criteria:

• Patients who underwent Previous surgical release

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
EPB entrapment test
Time Frame: 1 day
comparing the pain elicited during resisted thumb MCP joint abduction and resisted thumb MCP joint extension
1 day
Ultrasound examination of wrist
Time Frame: 1 day
musculoskeletal ultrasound of affected wrist is done for examining the anatomical variations of first extensor compartment
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Velammal Medical College Hospital and Research Institute

Investigators

  • Study Director: Srinivasan Rajappa, MS, DNB, Sri Ramachandra Institute of Higher Education and Research
  • Study Chair: Vijayaraja Elangovan, MS, Velammal medical college hospital and research institute
  • Principal Investigator: Gokul Kumar Jeganathan, MBBS, Velammal medical college hospital and research

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2020

Primary Completion (Actual)

July 8, 2022

Study Completion (Actual)

July 8, 2022

Study Registration Dates

First Submitted

January 8, 2023

First Submitted That Met QC Criteria

January 19, 2023

First Posted (Actual)

January 20, 2023

Study Record Updates

Last Update Posted (Actual)

January 20, 2023

Last Update Submitted That Met QC Criteria

January 19, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • VMCIEC/27/2022

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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