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NCT03155854 · ClinicalTrials.gov registry record · NA
The Effects of Prophylactic Limited Palmar Fasciectomy on Surgical Outcomes and Scarring
A NA study of Dupuytren Contracture, sponsored by Mayo Clinic.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT03155854 is a NA study of Dupuytren Contracture that is actively recruiting participants, run by Mayo Clinic. 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.
The verdict
NCT03155854, a NA study of Dupuytren Contracture, is actively recruiting participants, sponsored by Mayo Clinic.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
Research is instrumental for improving medical care and the patient experience. Finding new surgical techniques can create better outcomes and minimize recovery time and complications for patients. Some patients undergoing trigger finger surgery with a pre-existing Dupuytren's cord may develop a thickened surgical scar after surgery, which can cause discomfort, difficulty with moving or using, and other complications in the affected finger(s) or hand. The investigator is investigating a surgical technique to minimize these potential complications and scarring after surgery. Subjects are being asked to take part in this research study because they have been diagnosed with trigger finger and pretendinous Dupuytren's cord and have decided to undergo surgery rather than try medical treatment.
Conditions Studied
Interventions
- PROCEDURE Pretendinous cord excision
- PROCEDURE Division/manipulation of the cord
Study Locations (1)
Minnesota
- Mayo Clinic - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2016-09 |
| Est. Completion | 2026-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03155854
The ClinicalTrials.gov registry entry for NCT03155854 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 86-participant average among 4 other Dupuytren Contracture trials with a reported enrollment target (42% lower). The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Dupuytren Contracture appearing as the primary indexed condition, and to 2 interventions - of which Pretendinous cord excision is the first listed.
NCT03155854 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT03155854 about?
NCT03155854 is a clinical study titled "The Effects of Prophylactic Limited Palmar Fasciectomy on Surgical Outcomes and Scarring". Research is instrumental for improving medical care and the patient experience. Finding new surgical techniques can create better outcomes and minimize recovery time and complications for patients. Some patients undergoing trigger finger surgery with a pre-existing Dupuytren's cord may develop a thi...
What is the current status of trial NCT03155854?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2016-09. Estimated completion is 2026-12.
What conditions does trial NCT03155854 study?
This clinical trial studies the following conditions: Dupuytren Contracture.
What interventions are being tested in trial NCT03155854?
The interventions under investigation include: Pretendinous cord excision (PROCEDURE), Division/manipulation of the cord (PROCEDURE).
Who is sponsoring clinical trial NCT03155854?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03155854 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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Read our methodology - how this data is sourced, computed, and verified.
Related
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