Effectiveness of Night Splinting After Percutaneous Needle Fasciotomy in Dupuytren's Contracture
Study Details
Study Description
Brief Summary
Dupuytren's contracture (DC) is associated with progressive finger flexion and extension deficit caused by fibrosis in the palm and digits. Treatment options include minimally invasive procedures such as percutaneous needle fasciotomy (PNF) and collagenase clostridium histolyticum injections as well as open fasciectomy. PNF has recently become more popular in Sweden because it is an office-based procedure which is relatively easy to perform without the usual risks and costs of open surgery.
After treatment with PNF patients usually continue with supervised rehabilitation, which includes physical therapy and night splinting. Whether night splinting is beneficial in terms of reducing recurrence of DC is currently debated.
This study aims to investigate whether night splinting after performed PNF helps to reduce recurrence rate or not. Patients who meet the inclusion criteria will be randomized into two groups: The first group will be treated as usual with physical therapy and night splinting after PNF. The second group will be treated with physical therapy without night splinting after PNF. Follow up includes physical examination regarding active range of motion, sensation and grip strength at procedure day and 2 weeks, 3, 12 and 36 months later as well as questionnaires regarding hand function, pain and quality of life at procedure day and 3, 12 and 36 months later. Patients who are randomized into the second group (no night splinting) will also be examined 3 weeks after PNF for observation in case of an early impairment regarding extension deficit.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| No Intervention: Treatment with night splint after percutaneous needle fasciotomy
|
|
| Experimental: No treatment with night splint after percutaneous needle fasciotomy
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Other: No night splint
Instead of the usual treatment with a night splint for three months after percutaneous needle fasciotomy patients do not receive treatment with a night splint.
|
Outcome Measures
Primary Outcome Measures
- Reduction of finger joint contracture [at 1 year follow up]
Finger joint movement in order to extend the finger measured in degrees with a goniometer before and after treatment.
Secondary Outcome Measures
- Improvement of active finger flexion [before and after treatment, at 2 weeks, 3, 12 and 36 months follow-up]
Finger joint movement in order to flex the finger measured in degrees with a goniometer before and after treatment.
- Improvement of grip strength [before and after treatment, at 2 weeks, 3, 12 and 36 months follow-up]
The ability to grip with the hand measured with the Jamar hand dynamometer in kg before and after treatment.
- Pain assessed by a numeric rating scale (NRS) [before treatment, at 3, 12 and 36 months follow-up]
Report of pain in the treated finger using a numeric rating scale from 0 to 10, where 0 is equivalent to no pain at all and 10 is equivalent to the highest thinkable pain level.
- Quality of life assessed by EQ-5D [before treatment, at 3, 12 and 36 months follow-up]
Quality of life is measured by the EQ-5D questionnaire. This questionnaire is developed by the EuroQuol Group and measures 5 health dimensions: mobility, self care, usual activities, pain and discomfort, as well as anxiety and depression. The answers are transferred into an EQ-5D index from 0 to 1, where 0 is equivalent with the worst health state and 1 is equivalent with the best health state.
- Dupuytren-disease-associated disability assessed by URAM [before treatment, at 3, 12 and 36 months follow-up]
The URAM (Unité Rhumatologique des Affections de la Main) scale is a 9-item questionnaire for functional assessment in Dupuytren's disease with a range from 0-45 points, where 0 is equivalent with the best functional outcome and 45 is equivalent with the worst functional outcome.
- Semmes-Weinstein monofilament test [before treatment, at 3, 12 and 36 months follow-up]
Semmes-Weinstein monofilament test is a semi-quantitative test for sensory loss. Filaments in different sizes are used to put a different amount of pressure onto the skin. Depending on which filament size the patient is able to detect sensory loss can be investigated.
- Study specific questionnaire concerning the patient's medical history [before treatment, at 3, 12 and 36 months follow-up]
In this questionnaire the patient answers questions about present conditions such as diabetes and smoking, therapy with pain medication for the hand, how long the patient has been diagnosed with Dupuytren'd disease, if both hands are affected and if there is a positive family history.
Eligibility Criteria
Criteria
Inclusion Criteria:
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18 years of age and older,
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Palpable Dupuytren strand with passive extension deficit according to stadium 1 and 2 of the classification of Tubiana in one or two fingers excluding the thumb, defined as at least 30 degrees in the MCP joint and/or at least 20 degrees in the PIP joint and a maximum of 75 degrees in the MCP or PIP joint
Exclusion Criteria:
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Multiple, invasive or wide strands in the palm,
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Skin irritation,
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Strand localization in the digit only,
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Digital nerve injury,
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Any former treatment for Dupuytren's contracture in the same digit,
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Thumb contracture,
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Stadium 3 and 4 according to the classification of Tubiana
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Falu Lasarett | Falun | Dalarna | Sweden | 79182 |
| 2 | Akademiska Sjukhuset | Uppsala | Uppsala Län | Sweden | 75185 |
| 3 | Universitetssjukhuset Örebro | Örebro | Örebro Län | Sweden | 70185 |
Sponsors and Collaborators
- Uppsala University
Investigators
- Principal Investigator: Stephan Wilbrand, MD, PhD, Uppsala University
Study Documents (Full-Text)
More Information
Publications
None provided.- 2021-01331