Safety and Efficacy of Delayed Manipulation After Xiaflex Treatment in Subjects With Dupuytren's Contracture
Stopped early · Phase 4
Conditions studied: Dupuytren's Disease
In brief
The purpose of this study is to determine if of manipulation of digits following collagenase injection for treatment of Dupuytren's contracture is effected by the amount of time between injection and manipulation.
Key facts
- Study ID
- NCT01226121
- Run by
- Indiana Hand to Shoulder Center
- People needed
- 37
- Starts
- 2010-12-01
- Expected to finish
- 2012-12-01
- Last updated by the study team
- 2014-06-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adult subjects (> 18 years) of either gender with an metacarpophalangeal joint contracture and a palpable cord of > 20 degrees of a digit (excluding the thumb) due to Dupuytren's contracture
You may not qualify if…
- Any subject who has had prior surgical, percutaneous needle aponeurotomy or Xiaflex treatment for Dupuytren's contracture.
- Any subject using anti-coagulant therapy other than low dose aspirin (up to 150mg/day).
- Any subject in the opinion of the MD investigators with chronic, severe or terminal medical illness which would make them unsuitable for study participation.
- Any subject with known allergy to Xiaflex (Clostridial collagenase).
- Any subject who cannot conform to the study visit schedule
Where it is running
- Indiana Hand to Shoulder Center — Indianaplis, Indiana, United States
- Stony Brook University — Stony Brook, New York, United States
Full record on ClinicalTrials.gov
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