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Dupuytren´s Disease Study. Primary Disease, MCP Joint, Xiapex, PNF

A Randomized Controlled Trial (RCT) Comparing Clostridium Histolyticum With Needle Aponeurotomy.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02647619
Enrollment
80
Registered
2016-01-06
Start date
2013-10-31
Completion date
2022-04-30
Last updated
2022-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dupuytren Contracture

Keywords

Primary Dd disase, MCP joint

Brief summary

Aim: Clinical RCT comparing functional results and recurrence rate following enzymatic treatment vs. needle aponeurotomy. Materials and methods: 30° or more contracture of only one metacarpophalangeal (MCP) joint contracture of one of the three ulnar digits and less than 20° for the adjacent proximal interphalangeal (PIP) joint. Patients with primary disease of the hand. Total of 80 patients needed to detect difference of 13.5°. 1\) Needle aponeurotomy 2) Clostridium Histolyticum treatment. Clinical follow ups 1,4 weeks, 16 weeks and 1,2 and 5 years. Functional outcome scores: URAM, Quick Dash, EQ5D, brief MHQ, VAS pain and VAS patient satisfaction. Total passive extension contracture reduction, recurrence rate and registration of complications.

Detailed description

Open surgery (fascieectomy) has traditionally been considered the gold standard of treatment for Dupytren´s disease (Dd) despite considerable risk of complications. There is an increasing interest in Scandinavia in the treatment of Dd with Clostridium Histolyticum (Xiapex ®, Auxillium). However the enzyme is expensive and long-term effects are not well documented. More studies are needed to analyze both short and long term clinical outcome as well as cost-benefit analysis. The treatment arm of Xiapex in this study follows the recommendation as by the producer. The other treatment of Dd contracture in this study is needle fasiotomy/aponeurotomy. We use multiple perforation technigue with 26 G needle needle, with as little local anesthesia (xylocin w adrenaline) as needed during contionus extension of the finger untill successfully extended. The two procedures leave little scar tissue lessening the challenges posed by the reoperations. Recurrence rate of contracture following different treatments of Dupuytren's disease differs widely in the literature, and the rate is influenced by multiple factors.

Interventions

DRUGXiapex

Injection of collagenase of primary dupytren cord

26 G needle multiple perforation tecqnique with local anesthetic

Sponsors

University Hospital, Akershus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Primary Dd disease (no earlier treatment for this condition of the hand involved) * Single digit involvement, one of the three ulnar digits * Average norwegian language skills. * MCPJ contracture of 30 degrees or more and less than 20 degree involvement of the adjacent PIPJ * Minimum 18 y.o.

Exclusion criteria

* Involvement of 2 fingers/joints * Earlier treatment for Dd disease of the same hand, affection of addjecent PIPJ of 20 degrees or mor * Pregnancy * Ongoing treatment with platelet inhibitors * Treatment with tetracycline 2 weeks prior to treatment date * Poor norwegian language skills * Participation in other studies 4 weeks prior or after treatment date * Need to treat of both hands

Design outcomes

Primary

MeasureTime frame
Reduction in Total Passive Extension Deficit5 years

Secondary

MeasureTime frameDescription
EQ5D (Euroqol 5 Dimensions)5 years
Brief MHQ (Michigan Hand Questionare)5 years
URAM (Unité Rhumatologique des Affections de la Main)5 years
Jamar grip strength1,4,26 weeks and one year.
Quick Dash (Disabilities of the shoulder and Hand)5 years
VAS (Visual analogue sale) satisfaction1,4,26 weeks. 1,2 and 5 years0 is not satisfied, 10 maximum satisfied
Complications1,4,weeks One yearAE,SAE,SUSAR
Recurrence1,4,26 weeks. 1,2 and 5 yearsdef. 30 degrees of treated MCP joint, or 20 or more degrees of adjecent PIPJ
VAS (Visual analogue scale) pain1,4,26 weeks and one year0 is no pain, 10 maximum pain

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026