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Fasciectomy vs Collagenase Injection in Recurrent Dupuytren Disease

Primary Purpose

Dupuytren Disease of Finger

Status
Active
Phase
Phase 4
Locations
Sweden
Study Type
Interventional
Intervention
Fasciectomy
Collagenase Clostridium Histolyticum
Sponsored by
Region Skane
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dupuytren Disease of Finger

Eligibility Criteria

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

Inclusion Criteria:

  • Seeking treatment for recurrence of Dupuytren´s contracture in at least one finger.
  • Passive extension deficit of 30 degrees or greater in the metacarpophalangeal and/or proximal interphalangeal joint in a finger previously treated with surgical fasciectomy, collagenase injections, or needle fasciotomy.
  • Palpable cord in the palm and/or affected finger causing the recurrent contracture.
  • No Surgery, collagenase injection or needle fasciotomy in the finger with recurrent contracture in the past 12 months.

Exclusion Criteria:

  • Medical comorbidities that constitute a contraindication for surgical fasciectomy or collagenase injection.
  • Signs of nerve or vascular injury in the affected finger.
  • Osteoarthritis in the metacarpophalangeal and/or proximal interphalangeal joint joint in the affected finger
  • Complications after the previous treatment, such as infection or complex regional pain syndrome (CRPS).
  • Previous trauma or other surgery involving the affected finger.
  • More than 2 previous surgeries, collagenase injections or needle fasciotomies in the affected finger.
  • Examining surgeon deems further fasciectomy inappropriate or potentially associated with very high complication risk, for example in severe contracture and/or severe scarring after the previous surgeries and considers salvage procedures (such as amputation) as the more appropriate treatment.
  • Patient refusal to participate

Sites / Locations

  • Department of Orthopedics Hässleholm-Kristianstad

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Surgical fasciectomy

Collagenase Clostridium Histolyticum

Arm Description

Fasciectomy according to usual care (surgery), implying excision of Dupuytren's cords and tissues to release the finger joint contractures

Injection of 0.8 mg collagenase clostridium histolyticum into multiple spots in the Dupuytren cords followed by finger manipulation 1-2 days later to release the finger joint contractures

Outcomes

Primary Outcome Measures

Total active extension deficit (metacarpophalangeal plus proximal interphalangeal joints)
Extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Proportion of patients with worsening in total active extension deficit ≥20 degrees
Extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)

Secondary Outcome Measures

11-item disabilities of the arm, shoulder and hand (QuickDASH) score
A patient-reported outcome measure of activity limitations related to upper extremity disorders, with total score range from 0 (best) to 100 (worst)
EuroQoL 5-dimensions (EQ-5D) Index
Health-status and quality-of-life patient-reported measure, consists of 5 items, a single weighted score, the EQ-5D index, is calculated from the 5 dimensions, ranging from -0.594 (worst) to 1.0 (perfect health)
Pain score
Visual analog scale of pain in the treated hand, score range from 0 (best) to 100 (worst)
Satisfaction score
Visual analog scale of patient satisfaction with treatment outcome, score range from 0 (best) to 100 (worst)
Adverse events
All observed and reported adverse events will be recorded on a standard form. Serious adverse events include nerve, artery or tendon damage, deep infection, complex regional pain syndrome and any complications requiring surgery or hospital admission.
Costs
Total treatment cost, direct (medications, surgery, materials, visits etc) and indirect (sick leave related to the treatment)
Total active motion
Sum of active range of motion of metacarpophalangeal, proximal intephalangeal and distal interphalangeal joints of the treated finger
Total active extension deficit (metacarpophalangeal plus proximal interphalangeal joints)
Active extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Proportion of patients with worsening in total active extension deficit ≥20 degrees
Extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Palmar pain score
2-item scale inquiring about pain in the palm and related activity limitations, total score range 0 (best) to 100 (worst)
Cold intolerance symptom severity score
6-item scale inquiring about symptoms of cold intolerance, total score range 4 (best) to 100 (worst)
Total passive extension deficit (metacarpophalangeal plus proximal interphalangeal joints)
Passive extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)

Full Information

First Posted
January 14, 2018
Last Updated
October 24, 2022
Sponsor
Region Skane
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1. Study Identification

Unique Protocol Identification Number
NCT03406338
Brief Title
Fasciectomy vs Collagenase Injection in Recurrent Dupuytren Disease
Official Title
Surgical Fasciectomy Versus Collagenase Injection in Treating Recurrent Dupuytren Disease: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 20, 2018 (Actual)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
September 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Region Skane

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This randomized controlled trial will compare the outcome of surgery (fasciectomy) with that of local injection of Collagenase Clostridium Histolyticum in patients with recurrent finger joint contracture after previous treatment with Surgery, collagenase injection or needle fasciotomy. Half of the participants will be treated with surgery while the other half will receive collagenase injection.
Detailed Description
No definitive cure for Dupuytren disease (DD) currently exists and recurrence of finger contractures after treatment is common. Surgical fasciectomy is considered the standard treatment method for patients with recurrence. However, the procedure is associated with a high incidence of complications. Injection of Collagenase Clostridium Histolyticum into Dypuytren cords causing the contracture is a non-surgical treatment for DD and has been shown to be a safe and effective method. Most studies regarding collagenase injection have involved first-time treatment. Efficacy of collagenase injection in patients with recurrent DD, beyond the immediate effect, has not yet been determined. This randomized trial will compare the outcome of surgical fasciectomy and collagenase injection in treating patients with finger joints contracture due to recurrent DD. The study is a single-center randomized controlled trial. Patients referred to an orthopedic department are screened for eligibility. The inclusion criteria are recurrence of DD in one or more fingers after previous treatment with fasciectomy, collagenase injection or needle fasciotomy, a passive extension deficit ≥30 degrees in the metacarpophalangeal (MCP) and/or proximal interphalangeal (PIP) joint in a previously treated finger, and a palpable cord believed to cause the recurrent contracture. A total of 56 patients will be randomized (computer-generated randomization list, stratified according to type of previous treatment and affected finger), to either surgical fasciectomy or collagenase injection. A blinded hand therapist will measure range of motion (including active and passive extension deficit) at baseline and 3 months, 12 months, 24 months and 60 months after treatment. The primary outcomes are the total active extension deficit (MCP plus PIP) at 3 months and the proportion of patients with contracture worsening ≥20 degrees in the treated finger joint at 2 years compared to 3 months. The secondary outcomes include total passive extension deficit, the 11-item disabilities of the arm, shoulder and hand (QuickDASH) score, EuroQol 5-dimensions (EQ-5D) index, cold intolerance symptom severity score, palmar pain score, pain visual analog scale (VAS) score, satisfaction VAS score, adverse events and costs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dupuytren Disease of Finger

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized parallel Group, ratio 1:1.
Masking
Outcomes Assessor
Masking Description
Before examination the patients will wear thin gloves in the treated hands to conceal possible surgical scars so the examiner will be blinded to the group allocation.
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgical fasciectomy
Arm Type
Active Comparator
Arm Description
Fasciectomy according to usual care (surgery), implying excision of Dupuytren's cords and tissues to release the finger joint contractures
Arm Title
Collagenase Clostridium Histolyticum
Arm Type
Experimental
Arm Description
Injection of 0.8 mg collagenase clostridium histolyticum into multiple spots in the Dupuytren cords followed by finger manipulation 1-2 days later to release the finger joint contractures
Intervention Type
Procedure
Intervention Name(s)
Fasciectomy
Other Intervention Name(s)
Surgery
Intervention Description
Surgical excision of Dupuytren cords causing finger joint contractures. Surgery done under regional or general anesthesia. Additional procedures (such as capsulotomy or skin graft) done if surgeon deemed necessary.
Intervention Type
Drug
Intervention Name(s)
Collagenase Clostridium Histolyticum
Other Intervention Name(s)
Non-surgical treatment
Intervention Description
Injection of Collagenase into the Dupuytren cord after local anesthesia (nerve block) followed 24-48 hours later by finger manipulation after local anesthesia
Primary Outcome Measure Information:
Title
Total active extension deficit (metacarpophalangeal plus proximal interphalangeal joints)
Description
Extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Time Frame
Change from baseline to 3 months
Title
Proportion of patients with worsening in total active extension deficit ≥20 degrees
Description
Extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Time Frame
24 months compared to 3 months
Secondary Outcome Measure Information:
Title
11-item disabilities of the arm, shoulder and hand (QuickDASH) score
Description
A patient-reported outcome measure of activity limitations related to upper extremity disorders, with total score range from 0 (best) to 100 (worst)
Time Frame
Change over time from from baseline, 3 weeks, 6 weeks, 3 months, 12 months, 24 months and 60 months
Title
EuroQoL 5-dimensions (EQ-5D) Index
Description
Health-status and quality-of-life patient-reported measure, consists of 5 items, a single weighted score, the EQ-5D index, is calculated from the 5 dimensions, ranging from -0.594 (worst) to 1.0 (perfect health)
Time Frame
Change over time from from baseline, 3 weeks, 6 weeks, 3 months, 12 months, 24 months and 60 months
Title
Pain score
Description
Visual analog scale of pain in the treated hand, score range from 0 (best) to 100 (worst)
Time Frame
Change over time from from baseline, 3 weeks, 6 weeks, 3 months, 12 months, 24 months and 60 months
Title
Satisfaction score
Description
Visual analog scale of patient satisfaction with treatment outcome, score range from 0 (best) to 100 (worst)
Time Frame
3 weeks, 6 weeks, 3 months, 12 months, 24 months and 60 months
Title
Adverse events
Description
All observed and reported adverse events will be recorded on a standard form. Serious adverse events include nerve, artery or tendon damage, deep infection, complex regional pain syndrome and any complications requiring surgery or hospital admission.
Time Frame
Anytime during 24 months after treatment
Title
Costs
Description
Total treatment cost, direct (medications, surgery, materials, visits etc) and indirect (sick leave related to the treatment)
Time Frame
From baseline through 24 months
Title
Total active motion
Description
Sum of active range of motion of metacarpophalangeal, proximal intephalangeal and distal interphalangeal joints of the treated finger
Time Frame
Change from baseline to 3 months, 12 months, 24 months and 60 months
Title
Total active extension deficit (metacarpophalangeal plus proximal interphalangeal joints)
Description
Active extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Time Frame
Change from baseline to 12 months, 24 months and 60 months
Title
Proportion of patients with worsening in total active extension deficit ≥20 degrees
Description
Extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Time Frame
60 months compared to 3 months
Title
Palmar pain score
Description
2-item scale inquiring about pain in the palm and related activity limitations, total score range 0 (best) to 100 (worst)
Time Frame
Change over time from baseline to 3 weeks, 6 weeks, 3 months, 12 months, 24 months and 60 months.
Title
Cold intolerance symptom severity score
Description
6-item scale inquiring about symptoms of cold intolerance, total score range 4 (best) to 100 (worst)
Time Frame
Change from baseline to 3 weeks, 6 weeks, 3 months, 12 months, 24 months and 60 months.
Title
Total passive extension deficit (metacarpophalangeal plus proximal interphalangeal joints)
Description
Passive extension deficit of the metacarpophalangeal and interphalangeal joints of the treated finger measured with hand-held goniometer (0 degrees indicates no extension deficit)
Time Frame
Change from baseline to 24 months and 60 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Seeking treatment for recurrence of Dupuytren´s contracture in at least one finger. Passive extension deficit of 30 degrees or greater in the metacarpophalangeal and/or proximal interphalangeal joint in a finger previously treated with surgical fasciectomy, collagenase injections, or needle fasciotomy. Palpable cord in the palm and/or affected finger causing the recurrent contracture. No Surgery, collagenase injection or needle fasciotomy in the finger with recurrent contracture in the past 12 months. Exclusion Criteria: Medical comorbidities that constitute a contraindication for surgical fasciectomy or collagenase injection. Signs of nerve or vascular injury in the affected finger. Osteoarthritis in the metacarpophalangeal and/or proximal interphalangeal joint joint in the affected finger Complications after the previous treatment, such as infection or complex regional pain syndrome (CRPS). Previous trauma or other surgery involving the affected finger. More than 2 previous surgeries, collagenase injections or needle fasciotomies in the affected finger. Examining surgeon deems further fasciectomy inappropriate or potentially associated with very high complication risk, for example in severe contracture and/or severe scarring after the previous surgeries and considers salvage procedures (such as amputation) as the more appropriate treatment. Patient refusal to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isam Atroshi, MD, PhD
Organizational Affiliation
Lund University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Orthopedics Hässleholm-Kristianstad
City
Hässleholm
ZIP/Postal Code
SE 28125
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30808670
Citation
Nordenskjold J, Lauritzson A, Walden M, Kopylov P, Atroshi I. Surgical fasciectomy versus collagenase injection in treating recurrent Dupuytren disease: study protocol of a randomised controlled trial. BMJ Open. 2019 Feb 25;9(2):e024424. doi: 10.1136/bmjopen-2018-024424.
Results Reference
derived

Learn more about this trial

Fasciectomy vs Collagenase Injection in Recurrent Dupuytren Disease

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