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NCT04122313 · ClinicalTrials.gov registry record
Post-contracture Release Radiation for Dupuytren's Disease
A clinical trial of Dupuytren Contracture and Dupuytren's Disease, sponsored by University of Minnesota.
- Recruiting
- Registry status
- 50
- Enrollment target
- 1
- Study location
NCT04122313: Recruiting study of Dupuytren Contracture and Dupuytren's Disease, sponsored by University of Minnesota.
NCT04122313 is a study of Dupuytren Contracture and Dupuytren's Disease that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 50 participants, below the 86-participant average among 4 other Dupuytren Contracture trials with a reported enrollment target (42% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04122313, a study of Dupuytren Contracture and Dupuytren's Disease, is actively recruiting participants, sponsored by University of Minnesota.
- RECRUITING
- Registry status
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
To determine if the clinical impression of clinicians, ie that patients are improving with the current treatment pathway for Dupuytren's (contracture release followed by radiation), can be substantiated with scientific evidence.
Primary Outcome
The primary study endpoint is the patient's self-reported function which will be assessed using the validated Southampton Dupuytren's Scoring System (SDSS) questionnaire. The SDSS is a 5 item questionnaire with item scores ranging from 0 (no problem) to 4 (severe problem). Total scores are a sum of the 5 item scores with a total score range of 0 to 20. High scores indicate greater impairment due to the disease.
Conditions Studied
Interventions
- OTHER Evaluation of Dupuytren's Disease Treatment
Study Locations (1)
Minnesota
- University of Minnesota - Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2019-05-31 |
| Est. Completion | 2029-03-01 |
What NCT04122313 shows while recruiting
NCT04122313 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 86-participant average among 4 other Dupuytren Contracture trials with a reported enrollment target (42% lower).
The record links to 10 conditions, with Dupuytren Contracture appearing as the primary indexed condition, and to 1 intervention - of which Evaluation of Dupuytren's Disease Treatment is the first listed.
NCT04122313 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT04122313 about?
NCT04122313 is a clinical study titled "Post-contracture Release Radiation for Dupuytren's Disease". To determine if the clinical impression of clinicians, ie that patients are improving with the current treatment pathway for Dupuytren's (contracture release followed by radiation), can be substantiated with scientific evidence.
What is the current status of trial NCT04122313?
This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2019-05-31. Estimated completion is 2029-03-01.
What conditions does trial NCT04122313 study?
This clinical trial studies the following conditions: Dupuytren Contracture, Dupuytren's Disease, Dupuytren Disease of Palm and Finger, Dupuytren Disease of Finger, Dupuytrens Contracture of Both Hands.
What interventions are being tested in trial NCT04122313?
The interventions under investigation include: Evaluation of Dupuytren's Disease Treatment (OTHER).
Who is sponsoring clinical trial NCT04122313?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04122313 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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