Surgical technique to reduce scarring in trigger finger patients with Dupuytren's cord
The Effects of Prophylactic Limited Palmar Fasciectomy on Surgical Outcomes and Scarring for Dupuytren's Contracture Patients With Pretendinous Cord - Prospective Randomized Clinical Study (Pilot)
NA · Mayo Clinic · NCT03155854
This study is testing a new surgical method to help people with trigger finger and Dupuytren's cord heal better with less scarring after surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Mayo Clinic (other) |
| Locations | 1 site (Rochester, Minnesota) |
| Trial ID | NCT03155854 on ClinicalTrials.gov |
What this trial studies
This study investigates a new surgical approach for patients diagnosed with trigger finger who also have a Dupuytren's cord. The focus is on minimizing complications and scarring that can arise from traditional surgical methods. By excising the pretendinous cord, the study aims to alleviate tension and reduce the risk of adverse outcomes such as thickened scars and loss of motion. Patients who have opted for surgery after failing non-operative treatments will be included in the study.
Who should consider this trial
Good fit: Ideal candidates are adults diagnosed with trigger finger and a co-existing pretendinous Dupuytren's cord who have chosen surgical intervention.
Not a fit: Patients under 18 years of age will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved surgical outcomes and reduced scarring for patients undergoing trigger finger surgery.
How similar studies have performed: While similar surgical techniques have been explored, this specific approach to managing Dupuytren's cord in trigger finger surgery is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Potential candidates for the study will be selected based upon clinical diagnosis of trigger finger with co-existing pretendinous cord. All potential subjects will have either failed non operative treatment or elected surgical treatment. Exclusion Criteria: * \<18 years of age
Where this trial is running
Rochester, Minnesota
- Mayo Clinic — Rochester, Minnesota, United States (RECRUITING)
Study contacts
- Principal investigator: Sanjeev Kakar, MD — Mayo Clinic
- Study coordinator: Sanjeev Kakar, MD
- Email: Kakar.Sanjeev@mayo.edu
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Dupuytren Contracture