- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05675488
Ultrasound Features of Trigger Finger
August 11, 2023 updated by: Yasin Demir, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
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
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
-
-
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Ankara, Turkey
- Gaziler FTR EAH
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-
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
Additional Relevant MeSH Terms
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.
Clinical Trials on Trigger Finger
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Stanford UniversityTerminatedTrigger Finger | Trigger Finger Disorder | Trigger Thumb | Trigger Digit | Trigger Thumb, Left Thumb | Trigger Thumb, Right Thumb | Trigger Finger, Ring Finger | Trigger Finger, Index Finger | Trigger Finger, Middle Finger | Trigger Finger, Little Finger | Trigger Thumb, Unspecified Thumb | Trigger Finger, Unspecified...United States
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