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Injectable Collagenase and Percutaneous Needle Fasciotomy for Dupuytren's Contracture

Primary Purpose

Dupuytrens Contracture

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Xiapex
Percutaneous needle fasciotomy
Sponsored by
Jeppe Lange, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dupuytrens Contracture

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • DC affecting PIP joint with Passive Extension Deficit (PED) more than 20 degrees
  • Clearly defined strings

Exclusion Criteria:

  • Allergies to used medication
  • International Normalised Ratio more than 2.0
  • Pregnancy and breastfeeding
  • Previous treatment for DC in affected finger
  • Former inclusion in the study with another string
  • Activity in disease at time of study
  • PED more than 20 degrees for Metacarpophalangeal or Distal Interphalangeal joint in affected digit

Sites / Locations

  • Center for Planned surgery - Regionalhospital Silkeborg

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Collagenase injection

Percutaneous needle fasciotomy

Arm Description

Injection of collagenase obtained from Clostridium Histolyticum in contracture string

PNF ad modum Lermusiaux and Debeyre

Outcomes

Primary Outcome Measures

Clinical improvement
Clinical improvement is defined as a contracture reduction 50% or more from baseline.

Secondary Outcome Measures

Full Information

First Posted
February 18, 2012
Last Updated
October 3, 2016
Sponsor
Jeppe Lange, MD
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1. Study Identification

Unique Protocol Identification Number
NCT01538017
Brief Title
Injectable Collagenase and Percutaneous Needle Fasciotomy for Dupuytren's Contracture
Official Title
Comparing Injectable Collagenase (CI) and Percutaneous Needle Fasciotomy (PNF) for Dupuytren's Contracture (DC) Affecting Proximal Interphalangeal Joints (PIP). A Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jeppe Lange, MD

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Comparing injectable collagenase and percutaneous needle fasciotomy for Dupuytren's contracture affecting proximal interphalangeal joints. An open label, medico-independent randomized controlled trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dupuytrens Contracture

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Collagenase injection
Arm Type
Active Comparator
Arm Description
Injection of collagenase obtained from Clostridium Histolyticum in contracture string
Arm Title
Percutaneous needle fasciotomy
Arm Type
Active Comparator
Arm Description
PNF ad modum Lermusiaux and Debeyre
Intervention Type
Drug
Intervention Name(s)
Xiapex
Other Intervention Name(s)
XIAPEX® - Pfizer UK
Intervention Description
Collagenase Clostridium Histolyticum
Intervention Type
Procedure
Intervention Name(s)
Percutaneous needle fasciotomy
Intervention Description
Percutaneous needle fasciotomy ad modum Lermusiaux and Debeyre
Primary Outcome Measure Information:
Title
Clinical improvement
Description
Clinical improvement is defined as a contracture reduction 50% or more from baseline.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: DC affecting PIP joint with Passive Extension Deficit (PED) more than 20 degrees Clearly defined strings Exclusion Criteria: Allergies to used medication International Normalised Ratio more than 2.0 Pregnancy and breastfeeding Previous treatment for DC in affected finger Former inclusion in the study with another string Activity in disease at time of study PED more than 20 degrees for Metacarpophalangeal or Distal Interphalangeal joint in affected digit
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeppe Lange, M.D.
Organizational Affiliation
Regionshospitalet Silkeborg
Official's Role
Study Director
Facility Information:
Facility Name
Center for Planned surgery - Regionalhospital Silkeborg
City
Silkeborg
ZIP/Postal Code
8600
Country
Denmark

12. IPD Sharing Statement

Learn more about this trial

Injectable Collagenase and Percutaneous Needle Fasciotomy for Dupuytren's Contracture

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