CClinicalTrials.gg
Active, not recruitingNCT03192020DETECTUpdated Apr 29, 2026

Trial Comparing Treatment Strategies in Dupuytren's Contracture

A Phase 4 interventional study of Percutaneous needle fasciotomy (PNF) and Collagenase Clostridium Histolyticum (CCH) 2.9 MG/ML [Xiaflex] in Dupuytren Contracture, sponsored by Tampere University. Active, not recruiting at 6 sites in Finland. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-04-29.

Sponsored by Tampere University · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
302
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Trial is a prospective, randomized, controlled, outcome assessor-blinded, three armed parallel 1:1:1, multicenter trial. The research objective is to determine, which treatment strategy 1) primary percutaneous needle fasciotomy (PNF) followed by surgical limited fasciectomy (LF) in patients who do not respond to PNF, 2) primary collagenase clostridium histolyticym (CCH) followed by LF in patients who do not respond to CCH or 3) LF as the primary (and secondary) treatment modality is the most cost-effective in treating Dupuytren´s contracture. Short- and long-term results will be published.

Read the detailed description

Dupuytren's contracture (DC) is a fibroproliferative disorder of the palmar fascia, which in time leads to flexion contracture in one or more fingers. Etiology of the disease is still unknown, but it strongly seems that genetic factors play a major role. DC is associated most commonly with Caucasian population groups from Northern Europe. The estimated global prevalence among whites is 3% to 6% and increases with age. Men women ratio is 7:1. There is no definitive cure for DC. The treatment aims at relieving the symptoms by releasing the contracture by percutaneous or operative techniques.

The investigators planned a prospective, randomized, controlled, outcome assessor-blinded, three armed parallel 1:1:1, multicenter trial comparing the cost-effectiveness of 1) collagenase clostridium histolyticum followed by limited fasciectomy in non-responsive cases, 2) percutaneous needle fasciotomy followed by limited fasciectomy in non-responsive cases and 3) primary limited fasciectomy in short- and long-term follow-up in DC.

Protocol is approved by Tampere university hospital institutional review board and Finnish Medicine Agency (Fimea). All patients will give written informed consent. The results of the trial will be disseminated as published articles in peer-reviewed journals.

Treatment of Duputren's contracture aims at reducing the functional deficit caused by the contracture. Recurrence is almost inevitable if the follow-up is long enough. Therefore, the investigators aim to analyze the effectiveness of three different treatment strategies in long-term follow-up, in addition to short-term follow-up, which include multiple interventions rather than just single intervention. The investigators chose a pragmatic primary outcome, which comprises both objective and subjective standpoint and reflects the needs of the patients as well as goals of the healthcare system. Furthermore, our short-term results give good high quality level evidence of effectiveness of all the three treatments and long-term follow-up a good perspective to the cost-effectiveness of the strategies.

02

Conditions studied

  • Dupuytren Contracture

Keywords

  • Hand
  • Xiapex
  • Xiaflex
  • Clostridium histolyticum collagenase
  • Needle
  • Surgery
  • Aponeurectomy
  • Aponeurotomy
  • Fasciotomy
  • Fasciectomy
  • Dupuytren's disease
  • Dupuytren's contracture
  • Contracture
  • Connective tissue disease
03

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • patients with ≥20° passive extension deficit in metacarpophalangeal (MPJ) or proximal interphalangeal joint (PIPJ), or TPED ≥30° in MPJ and PIPJ of finger/fingers II-V
  • age > 18 years
  • palpable cord
  • provision of informed consent
  • ability to fill the Finnish versions of questionnaires.

Exclusion criteria

Exclusion Criteria:

  • recurrent contracture in the finger to be treated
  • neurologic condition causing the loss of function of the finger to be treated
  • contraindication for collagenase clostridium histolyticym (Xiapex/Xiaflex ®)
  • pregnant or breast feeding
  • total passive extension deficit > 135° (Tubiana stage 4) in finger to be treated
  • rheumatoid arthritis
  • previous fracture in finger to be treated, which affects range of motion of MPJ or PIPJ
  • age > 80 years
04

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
302 participants (actual)

Study arms

  • Experimental
    Percutaneous needle fasciotomy (PNF)

    PNF is a treatment in which the Dupuytren's contracture cord causing the contracture is not excised, but only divided with a hypodermic needle.

    Procedure: Percutaneous needle fasciotomy (PNF) · Procedure: Limited fasciectomy (LF)

  • Experimental
    Collagenase clostridium histolyticum (CCH)

    Generic name of the drug is collagenase clostridium histolyticum. Dosage form is injectable powder, dosage 0.58 mg and frequency is one injection in four weeks up to three times. One injection is performed normally at least to three different places in the cord.

    Drug: Collagenase Clostridium Histolyticum (CCH) 2.9 MG/ML [Xiaflex] · Procedure: Limited fasciectomy (LF)

  • Active comparator
    Limited fasciectomy (LF)

    In LF, the thickened part of the palmar fascia causing the contracture is excised through skin incision.

    Procedure: Limited fasciectomy (LF)

Interventions

  • ProcedurePercutaneous needle fasciotomy (PNF)

    The division of the cord can be made under local anesthesia in the clinic and takes only a few minutes to perform. It can be performed whenever the cord is palpable. There are only puncture wounds left, and hence, the patient can start normal use of the hand the day after the procedure. If patient seeks for a treatment and the recurrence of the disease can not be treated by the PNF or patient is not willing to new PNF patient will be treated with LF.

    Also known as: Percutaneous needle aponeurotomy

  • DrugCollagenase Clostridium Histolyticum (CCH) 2.9 MG/ML [Xiaflex]

    CCH chemically dissolves type I collagen of which the cord is composed of. It is injected inside the cord at least three different places in the outpatient clinic and the cord can be ruptured by gently force after one to three days. If patient seeks for a treatment and the recurrence of the disease can not be treated by the CCH or patient is not willing to new CCH patient will be treated with LF.

    Also known as: [Xiapex]

  • ProcedureLimited fasciectomy (LF)

    LF is performed in general or regional anesthesia in operating room. Constricting cords will be excised under direct vision. LF has been the dominant technique of surgical treatment. If patient seeks for a treatment the recurrence of the disease will be treated with LF as long as needed.

    Also known as: Limited aponeurectomy

05

What researchers measure

Primary outcomes

  1. Rate of success

    Success is a composite outcome comprising of 1) at least 50% contracture release from the recruitment and 2) patient is in patient accepted symptom state (PASS). PASS is defined by question: "Would you be satisfied and not in need for any other treatment if the functional impairment caused by the contracture would remain the same as it is today for the rest of your life?". Primary time point is five years' follow-up visit.

    Time frame: 5 year follow-ups

Secondary outcomes

  1. QuickDASH

    QuickDASH questionnaire is a validated upper extremity specific questionnaire consisting of 11 tasks/questions about the functional capacity and the pain.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  2. Perceived hand function

    Perceived hand function will be assessed pre- and postoperatively by VAS scale.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  3. Global rating

    Global rating to treatment effect will be evaluated by question: "How would you rate the function of your hand compared to the situation before the treatment?". The options are in 5-step Likert scale from (-2) Much worse to (+2) Much better: This question is also used as anchor question in the MCII analysis in which +1 and +2 are considered to present meaningful improvement to the patient.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  4. EQ-5D-3L

    EQ-5D-3L is a generic instrument for assessing quality of life comprising 5 dimensions and VAS for health level.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  5. Rate of Patient Accepted Symptom State

    PASS is a relevant patient-centered outcome measurement, which reflects the overall state in which patients consider themselves as being well. It is a state of the symptoms between complete remission and subjective dissatisfaction with the symptoms.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  6. Rate of patients achieving clinically significant improvement

    Percentage of patients achieving clinically significant improvement (50% better PED) will be assessed.

    Time frame: 10 year follow-up

  7. Rate of patients achieving full contracture release

    Percentage of patients achieving full contracture release (PED 0°-5°) will be assessed.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  8. Willingness to undergo same treatment

    Patient satisfaction with the treatment will be assessed by a simple "yes" or "no" question: "Would you prefer the same treatment again, if the result would be the same as it is now?"

    Time frame: 3 months and 2 year follow-ups

  9. Major adverse events

    In the trial will be reported major adverse events, which include: tendon rupture, nerve injury, arterial injury, CRPS and infection, skin rupture or hematoma that needs hospitalization/revision surgery.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  10. Extension deficits

    The total passive extension deficit (TPED) and passive extension deficit (PED) of metacarpophalangeal (MPJ) and proximal interphalangeal (PIPJ) joints are used in almost all of the DC studies. Most of the studies used the PED as their primary outcome. In this trial, the TPED and PED of MPJ and PIPJ are used as secondary outcomes.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  11. Total maximum flexion

    Patients are seeking help for their extension deficit in DC but in the end flexion of the fingers is more important for the hand function. Our treatments should not jeopardize finger flexion in an effort to reduce the extension deficit.

    Time frame: 3 months, 2, 5 and 10 year follow-ups

  12. Expenses

    The costs are assessed by allocating previously estimated costs for interventions to each of the treatment arm.

    Time frame: 2, 5 and 10 year follow-ups

  13. Progression of the disease

    Recurrence or extension is treated if the patient contacts the study center and requires new treatment (ie, patient is not in the PASS anymore) and at least 20° flexion contracture is observed in one of the joints. Progression of disease is measured and reported in three levels: (1) rate of reinterventions in the arm due to recurrence or extension of the disease (clinically relevant progression); (2) costs of reinterventions (impact of progression); and (3) change in TPED in those patients who do not require further treatments (clinically irrelevant progression).

    Time frame: 2, 5 and 10 year follow-ups

  14. Recurrence of the disease

    In this study recurrence is defined when patient considers not being in PASS anymore and seeks for further treatment, and has at least 20° contracture.

    Time frame: 2, 5 and 10 year follow-ups

  15. Extension of the disease

    Extension means that the disease will be activated in other rays than treated after the treatment.

    Time frame: 2, 5 and 10 year follow-ups

  16. Progression-free-survival

    Progression-free-survival will be counted to each arm as mean time.

    Time frame: 2, 5 and 10 year follow-ups

  17. Favored treatment modality questionnaire

    Favored treatment modality will be asked from patients who undergo several treatment modalities (i.e. LF after CCH or PNF). Outcome will be assessed by question: "If you presented with a contracture for the first time now, would you prefer needle fasciotomy/injectable drug as the primary treatment or would prefer having surgery at first place?"

    Time frame: 2, 5 and 10 year follow-ups

  18. Rate of success

    Success is a composite outcome comprising of 1) at least 50% contracture release from the recruitment and 2) patient is in patient accepted symptom state (PASS). PASS is defined by question: "Would you be satisfied and not in need for any other treatment if the functional impairment caused by the contracture would remain the same as it is today for the rest of your life?". Primary time point is five years' follow-up visit.

    Time frame: 3 months, 2 and 10 year follow-ups

06

Study locations

6 sites
  • Central Hospital of Central Finland
    Jyväskylä, Central Finland 40620, Finland
  • Oulu University hospital
    Oulu, North Ostrobothnia 90220, Finland
  • Kuopio University hospital
    Kuopio, Northern Savonia 70029, Finland
  • Tampere University Hospital
    Tampere, Pirkanmaa 33521, Finland
  • Turku University Hospital
    Turku, Southwest Finland 20521, Finland
  • Helsinki University hospital
    Helsinki, Uusimaa 00029, Finland
07

References and documents

Publications

  • Raisanen MP, Karjalainen T, Goransson H, Reito A, Kautiainen H, Malmivaara A, Leppanen OV. DupuytrEn Treatment EffeCtiveness Trial (DETECT): a protocol for prospective, randomised, controlled, outcome assessor-blinded, three-armed parallel 1:1:1, multicentre trial comparing the effectiveness and cost of collagenase clostridium histolyticum, percutaneous needle fasciotomy and limited fasciectomy as short-term and long-term treatment strategies in Dupuytren's contracture. BMJ Open. 2018 Mar 28;8(3):e019054. doi: 10.1136/bmjopen-2017-019054. PubMed 29599391 ↗
  • Raisanen MP, Leppanen OV, Soikkeli J, Reito A, Malmivaara A, Buchbinder R, Kautiainen H, Kaivorinne A, Stjernberg-Salmela S, Lappalainen M, Luokkala T, Ponkko A, Taskinen HS, Paakkonen M, Jaatinen K, Juurakko J, Karjalainen VL, Karjalainen T. Surgery, Needle Fasciotomy, or Collagenase Injection for Dupuytren Contracture : A Randomized Controlled Trial. Ann Intern Med. 2024 Mar;177(3):280-290. doi: 10.7326/M23-1485. Epub 2024 Feb 13. PubMed 38346307 ↗
  • Karjalainen VL, Soikkeli J, Raisanen MP, Leppanen OV, Reito A, Stjernberg-Salmela S, Buchbinder R, Karjalainen T. Progression of Dupuytren Contracture: A Randomized Controlled Trial Comparing Surgery, Needle Fasciotomy, and Collagenase Injection. Plast Reconstr Surg. 2026 Jul 1;158(1):101-112. doi: 10.1097/PRS.0000000000012666. Epub 2025 Dec 4. PubMed 41334972 ↗

Study documents

  • Informed consent form · Mar 29, 2017

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — All the IPD will be shared with other researchers by request.

Supporting information: Study protocol, Sap, Icf, Analytic code

08

Registry details

Key details

Study ID
NCT03192020
Lead sponsor
Tampere University
Collaborators
Central Finland Hospital District, Helsinki University Central Hospital, Turku University Hospital, Tampere University Hospital, Kuopio University Hospital, Oulu University Hospital, Medcare Oy, Finnish Institute for Health and Welfare, Orton Orthopaedic Hospital
Responsible party
Olli Leppänen (M.D., Ph.D., Tampere University) — Principal investigator
First posted
Jun 19, 2017
Start date
Sep 15, 2017
Primary completion
May 31, 2026 (estimated)
Completion
May 31, 2031 (estimated)
Last update
Apr 29, 2026

Study contacts

Mikko P Räisänen, M.D.
principal investigator · Tampere University Hospital
Harry J Göransson, M.D., Ph.D., adjunct professor
principal investigator · Tampere University Hospital
Aleksi RP Reito, M.D., Ph.D., adjunct professor
principal investigator · Central Finland Hospital District
Hannu Kautiainen, MSc
principal investigator · Medcare Ltd
Antti OV Malmivaara, M.D., Ph.D., adjunct professor
principal investigator · Finnish Institute for Health and Welfare

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion