Clinical trial

A Multi-Center, Randomized Controlled Trial Comparing The Clinical Effectiveness and Cost-Effectiveness of Collagenase Injection (Xiaflex) and Palmar Fasciectomy in the Management of Dupuytren's Disease

Name
PSI 2016-03
Description
This is a prospective, multi-centre, pragmatic randomized controlled trial to compare both the clinical effectiveness and cost-effectiveness of collagenase injections (CI) versus limited palmar fasciectomy (LPF) to determine if collagenase is a superior treatment in terms of improved quality of life and reducing recurrence of the disease without serious complications. Since collagenase injections are costly it is also important to know if this novel intervention is cost-effective from the patient, Ministry of Health and societal perspectives.
Trial arms
Trial start
2017-07-08
Estimated PCD
2021-12-17
Trial end
2021-12-17
Status
Completed
Phase
Early phase I
Treatment
collagenase injection
injection
Arms:
collagenase injection
Other names:
enzyme, collagenase clostridium histolyticum, xiaflex
limited palmar fasciectomy
surgery
Arms:
limited palmar fasciectomy
Size
22
Primary endpoint
Health-related Quality of Life (HRQL) Using the Michigan Hand Outcomes Questionnaire (MHQ)
1 year
Eligibility criteria
Inclusion Criteria: 1. Canadian Citizen 2. 18 years of age or older 3. Dupuytren's contracture of the metacarpophalangeal (MCP) joint or of the proximal interphalangeal (PIP) joint with a fixed flexion contracture of 20º or greater in at least 1 finger (not the thumb) 4. Demonstrated inability to simultaneously place the affected finger and palm flat on a table 5. Able to understand and communicate in English Exclusion Criteria: 1. Previous treatment of the primary joint within 90 days of study inclusion 2. Patients undergoing any concomitant procedure on the same hand (e.g. carpal tunnel release, stenosing tenosynovitis release) 3. Persistent extension deficit from a previous surgery of the same digit 4. Any chronic muscular or neuromuscular disorder affecting wrist or hand 5. Patient generally unfit for surgery 6. Patient with specific treatment preference 7. Bleeding disorder or recent stroke 8. Allergy to collagenase 9. Collagenase treatment or treatment with any investigational drug within 30 days of study inclusion 10. Use of a tetracycline derivative within 14 days of first dose of study drug (because tetracycline derivatives may inhibit the collagenolytic activity of mammalian collagenase homologs \[i.e., matrix metalloproteinases\]) 11. Pregnant or breast feeding patients 12. Patients who do not have insurance coverage for collagenase injections 13. Patients who are unable to provide informed consent or are unable to complete quality of life questionnaires due to mental capacity or neuro-psychological problems.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 22, 'type': 'ACTUAL'}}
Updated at
2023-07-18

1 organization

1 product

1 indication