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Percutaneous Needle Fasciotomy +/- Corticosteroid Injection for Dupuytren's Contracture

Launched by REGIONSHOSPITALET SILKEBORG · Jun 27, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Percutaneous Needle Fasciotomy Corticosteroid Randomized Controlled Trial

ClinConnect Summary

This clinical trial is studying a treatment for Dupuytren's contracture, a condition that causes the fingers to bend toward the palm due to thickened tissue. Researchers want to compare two approaches: one that uses a special needle to loosen the tight tissue (called percutaneous needle fasciotomy) and another that combines this procedure with a corticosteroid injection. The goal is to see which method is more effective in helping people regain movement in their fingers.

To participate in this study, individuals should be between 16 and 99 years old and have Dupuytren's contracture that causes at least 20 degrees of bending in their finger joints. Participants will undergo the treatment, and their progress will be monitored. It's important to note that certain conditions may prevent someone from joining, such as previous hand surgeries or certain medical issues. Overall, this trial aims to find better ways to treat Dupuytren's contracture and improve patients' quality of life.

Gender

ALL

Eligibility criteria

  • Sufficient correction of metacarpophalangeal (MCP) joint during the PNF treatment, defined as \<20° passive extension deficit (PED), is a prerequisite for inclusion.
  • Inclusion Criteria:
  • Dupuytren contracture (DC) of ≥ 20° PED in MCP joint measured with a goniometer
  • DC of either II-V finger
  • Well-defined/palpable cord
  • Exclusion Criteria:
  • Legally incapacitated
  • Previous study inclusion with another finger ray
  • Isolated proximal interphalangeal (PIP) or distal interphalangeal (DIP) joint contracture, defined as MCP joint contracture \< 20° PED regardless of the deficit in the PIP or DIP joint
  • Previous hand surgery of the affected finger for any reason
  • Known allergy to the study medication
  • Anticoagulant therapy (Acetylsalicylic acid is NOT an exclusion criterion)
  • Pregnant or lactation
  • Insulin dependent diabetes mellitus
  • Ongoing systemic infection or local infection at the site of the procedure
  • Rheumatoid arthritis
  • Amyloidosis or mucopolysaccharidosis
  • Unable to communicate, cooperate or participate in follow-up

About Regionshospitalet Silkeborg

Regionshospitalet Silkeborg is a leading healthcare institution in Denmark, dedicated to providing high-quality medical care and advancing clinical research. As a prominent sponsor of clinical trials, the hospital focuses on innovative treatments and therapies, aiming to enhance patient outcomes and contribute to the scientific community. With a multidisciplinary team of experienced healthcare professionals and researchers, Regionshospitalet Silkeborg is committed to ensuring rigorous study protocols and ethical standards, fostering collaboration, and driving advancements in medical knowledge and practice.

Locations

Silkeborg, , Denmark

Patients applied

0 patients applied

Trial Officials

Jeppe Lange, MD, PhD

Study Director

Regionshospitalet Horsens

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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