Clinical Trials Directory

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UnknownNCT02301078

Short-term Function and Pain After Treatment for Dupuytren's Disease

Comparing Short-term Function and Pain After Treatment With Collagenase Clostridium Histolyticum or Percutaneous Needle Aponeurotomy for Dupuytren's Disease

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Sunnybrook Health Sciences Centre · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate short-term pain and function associated with percutaneous needle aponeurotomy (PNA) and injections of the enzyme collagenase clostridium histolyticum in patients with Dupuytren's disease. Scores on outcome measures will be compared between groups to determine whether treatments differ in terms of hand function and pain during the early post-treatment period.

Detailed description

Percutaneous needle aponeurotomy (PNA) and injections of the enzyme collagenase clostridium histolyticum are two non-invasive treatment options for patients with Dupuytren's disease. While PNA has been offered for decades, injectable collagenase is relatively new. The effectiveness of each treatment has been compared in the literature; however, recovery, in terms of pain and short-term function has not been formally evaluated. The objective of this study is to objectively compare short-term function and pain outcomes associated with each of these two procedures in patients presenting with untreated Dupuytren's disease.

Conditions

Interventions

TypeNameDescription
PROCEDUREPercutaneous Needle Aponeurotomysingle procedure (day 0)
DRUGCollagenase clostridium histolyticumXiaflex injection into palpable cords (day 0), physical manipulation (day 7)

Timeline

Start date
2014-07-01
Primary completion
2017-10-01
Completion
2017-11-01
First posted
2014-11-25
Last updated
2016-12-06

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02301078. Inclusion in this directory is not an endorsement.