Dupuytren's Disease and Extracorporeal Shockwave Therapy (DupuyShock-2010) (DupuyShock)
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|ClinicalTrials.gov Identifier: NCT01184586|
Recruitment Status : Unknown
Verified December 2011 by Karsten Knobloch, Hannover Medical School.
Recruitment status was: Recruiting
First Posted : August 19, 2010
Last Update Posted : December 2, 2011
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Dupuytren's disease is a progressive disease due to unknown causal agents or genetics.
Dupuytren's disease contains nodules and cords in the fascia as the epicenter of disease progression. Nodules contain whorls of collagen bundles and are densely packed with contractile fibroblasts and myofibroblasts. These highly contractile cells are linked to the fascia matrix through transmembrane integrin receptors. The cytoplasmic tail domains of the alpha beta integrin receptors provide a structural link between extracellular matrix and the actomyosin cytoskeleton.
Complications of surgical partial or total aponeurectomy in Dupuytren's disease are reported in up to 10% of cases . Often, surgical complications lead to compromised flexion limiting grasping function of the involved hand . A recent 20-year-review of the literature included 41 clinical trials with complication rates reported from 3.6%to 39.1% . 16% major complications occurred with 3% digital nerve injuries, digital artery injuries in 2%, infections in 2%, and complex regional pain syndrome in 6%. Besides selective or total aponeurectomy, soft-tissue distraction has been suggested using either pneumatic devices or external fixateur .
Non-invasive options include percutaneous fasciotomy or collagenase injection. The latter has been tested in a randomized-controlled trial published in the New England Journal of Medicine with 308 patients enrolled (NCT00528606) . Collagenase clostridium histolyticum significantly reduced contractures and improved the range of motion in joints affected by advanced Dupuytren's disease. In the long-term the cords at the level of the proximal interphalangeal joint appear to more recurrent than at the metacarpophalangeal joint after collagenase injection with an eight year follow-up .
In early stage Dupuytren's contracture, radiotherapy has been suggested to limit disease progression. A cohort study of 135 patients with 208 hands involved received orthovoltage radiotherapy with a total dose of 30Gray separated by a six to eight week interval . After a follow-up of 13 years nodules and cords remained stable in 59%, improved in 10% and progressed in 31%.
Beside Dupuytren's disease, there are a number of further less common fibromatosis, such as knuckle pads, M. Ledderhose , of the plantar fascia and peyronie disease at the penis. The latter has been treated by extracorporeal shockwave therapy. A randomized-controlled trial using 2000 focused shock waves reduced pain significantly and improved erectile function and quality of life . About half of the patients in one series of 44 patients had a significant reduction in angulation following shockwave therapy .
|Condition or disease||Intervention/treatment||Phase|
|Dupuytren Contracture||Device: Intervention - ESWT Storz Duolith high energy Device: CONTROL SHAM-ESWT Storz Duolith [0.01mJ/mm2]||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||60 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Outcomes Assessor)|
|Official Title:||Dupuytren's Disease and Extracorporeal Shockwave Therapy (DupuyShock-2010) - a Randomized Trial|
|Study Start Date :||November 2011|
|Estimated Primary Completion Date :||December 2012|
|Estimated Study Completion Date :||December 2012|
Active Comparator: Intervention arm - ESWT Storz Duolith high energy
Three weekly sessions of extracorporeal shockwave therapy with focussed shock waves (STORZ DUOLITH, 1000 impulses, 0.55-0,8mJ/mm2)
Device: Intervention - ESWT Storz Duolith high energy
Three weekly sessions of extracorporeal shockwave therapy with focussed shock waves (2000 impulses, 0,35-1,25mJ/mm2)
Sham Comparator: Control - SHAM ESWT STORZ DUOLITH [0.01mJ/mm2]
Three weekly sessions of sham extracorporeal shock wave with modified probe without shockwave transduction (1000 impulses)
Device: CONTROL SHAM-ESWT Storz Duolith [0.01mJ/mm2]
Three weekly sessions of sham extracorporeal shock wave (2000 impulses, 0,01mJ/mm2)
- Score of Michigan Hand Outcome Questionnaire (MHQ) [0=poor, 100= perfect] [ Time Frame: 12 weeks ]The MHQ is a side-specific questionnaire with 25 unilateral and 12 bilateral questions, including hand function, work performance, and cosmetic appearance. It generates a score from 0 (poor) to 100 (no disability at all). The MHQ is responsive to clinical change. We have performed a validated standardized language adoption of the English MHQ into German, published in Plastic Reconstructive Surgery (Knobloch K et al. PRS 2010 in press).
- DASH Score [0=perfect, no impairment, 100=worst] [ Time Frame: 12 weeks ]The DASH is a 30-item patient-reported questionnaire with two adjuncts, DASH-Sport (4 items) and DASH-Work (4-items). Notably, the validation of the aformentioned DASH score included patients suffering from Dupuytren's disease. Longitudinal construct validity has been assessed in patients including those with Dupuytren's disease and the responsiveness is moderate (effect size 0,5). The DASH questionnaire has a good validity with the subscale of SF-36 . The test-retest reliability of the DASH questionnaire has been found to be excellent (ICC = 0.96) .
- Range of motion [ROM°] [ Time Frame: 12 weeks ]Range of motion (ROM) measured in [°] using a goniometer
- Grip strength [JAMAR] [ Time Frame: 12 weeks ]Hand grip strength [kg] using a JAMAR dynanometer in three repetitions on each hand with elbow totally extended (0° flexion) and 90° flexion
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|Ages Eligible for Study:||18 Years to 80 Years (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Eligible patients are patients aged 18 or over and 80 or younger
- Dupuytren's disease of stage 1-4 involving one or more fingers or the palm only
- Exclusion criteria are suspected or evident pregnancy
- no Dupuytren's disease
- evident ulcerations
- no informed consent
- age under 18 years or above 80 years.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01184586
|Contact: Karsten Knobloch, MD||0049511532 ext email@example.com|
|Contact: Marie Kuehn||0049511532 ext 8864||Marie.Kuehn@stud.mh-hannover.de|
|Hannover Medical School, Plastic, Hand and Reconstructive Surgery||Recruiting|
|Hannover, Germany, 30625|
|Contact: Karsten Knobloch, MD, FACS 00495115328864 firstname.lastname@example.org|
|Principal Investigator: Karsten Knobloch, MD|
|Principal Investigator:||Karsten Knobloch, MD||Hannover Medical School, Germany|
|Study Chair:||Peter M Vogt, MD, PhD||Hannover Medical School, Germany|
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
|Responsible Party:||Karsten Knobloch, Prof. Dr. Karsten Knobloch, FACS, Hannover Medical School|
|Other Study ID Numbers:||
|First Posted:||August 19, 2010 Key Record Dates|
|Last Update Posted:||December 2, 2011|
|Last Verified:||December 2011|
Neoplasms, Fibrous Tissue
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Connective Tissue Diseases