Ultrasound Features of Trigger Finger

Ultrasound Features of Trigger Finger: A Comparative Study With Healthy Volunteers

Our aim in this study; to compare the ultrasound findings seen in trigger finger patients with healthy volunteers. Thus, ultrasound findings associated with trigger finger development will be documented

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

A1 pulley thickness, flexor tendon thickness, and presence of nodules at the MCP joint level of the trigger finger patients will be recorded. The same measurements will be made in age- and sex-matched healthy volunteers, followed by comparison and analysis.

Study Type

Observational

Enrollment (Actual)

60

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

      • Ankara, Turkey
        • Gaziler FTR EAH

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

Yes

Sampling Method

Non-Probability Sample

Study Population

A total of 30 patients with trigger finger and 30 age and BMI-matched healthy controls

Description

Inclusion Criteria:

  • Aged over 18 years
  • To have trigger finger (for patient group)
  • Not to have trigger finger (for healthy group)

Exclusion Criteria:

  • Aged under 18
  • Wound or infection in the imaging area

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: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Healthy individuals
Thickness of flexor tendon and A1 pulley at MCP joint level
Trigger Finger Patients
Thickness of flexor tendon and A1 pulley at MCP joint level

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Thickness of flexor tendon
Time Frame: through study completion, an average of one and a half months
Thickness of flexor tendon at MCP joint level
through study completion, an average of one and a half months
Thickness of A1 pulley
Time Frame: through study completion, an average of one and a half months
Thickness of A1 pulley at MCP joint level
through study completion, an average of one and a half months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Presence of nodules
Time Frame: through study completion, an average of one and a half months
Presence of nodule in flexor tendon
through study completion, an average of one and a half months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Yasin Demir, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

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)

January 14, 2023

Primary Completion (Actual)

June 15, 2023

Study Completion (Actual)

August 7, 2023

Study Registration Dates

First Submitted

December 29, 2022

First Submitted That Met QC Criteria

December 29, 2022

First Posted (Actual)

January 9, 2023

Study Record Updates

Last Update Posted (Actual)

August 14, 2023

Last Update Submitted That Met QC Criteria

August 11, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 31 (Other Identifier: IASO Thessalias)

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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