No registrations found.
ID
Source
Brief title
Health condition
Secondary/ recurrent Dupuytren's disease
Sponsors and support
Intervention
Outcome measures
Primary outcome
1. Convalescence (in days): VAS, 6 questions (diary);
2. Contracture reduction (in degrees): range motion (in degrees), boyes measure (in cm.), pictures.
Secondary outcome
1. Intervention (Register the anaesthetics drugs administered and vital signs during surgery, no protocol is used; Register the therapy used for PIP joint);
2. Hand sensibility and complications due to intervention: semmes weinstein ( 5 filaments (2.83; 3.61; 4.31; 4.56; 6.65)), volume (in cm.), DASH;
3. Patient satisfaction (VAS scale);
4. MRI and Echo (selection of the intervention group).
Background summary
Dupuytren’s disease (DD) is a benign, progressive, fibroproliferative disorder that results in the development of abnormal scar-like tissue in the palmar fascia of the hand. Extension to the digits causes progressive digital flexion contracture[1, 2]. In 2006, Dupuytren’s disease was diagnosed 7048 times in the Netherlands. In total, 5843 DD operations were performed that year (Prismant Informatie Expertise). The treatment of DD mainly consists of surgery. Accepted options for managing diseased skin and fascia are (1) limited fasciectomy, (2) segmental fasciectomy (3) fasciotomy (4) dermofasciectomy. Limited fasciectomy and, if necessary, limited dermofasciectomy are the most often-used techniques[3]. With this technique, full recovery of hand function generally takes 2-3 months. In collaboration with the Miami Hand Center (Roger K. Khouri, MD), we developed a technique in which percutaneous release of fibrotic cords is refined in combination with subdermal fat grafting. Subdermal dissection of the cord is performed by making multiple superficial nicks along the entire cord. The cord then chops, disintegrates and separates from the dermis. This space is filled with fat grafts. This technique should have a shorter convalescence because it is less invasive compared with the conventional techniques. Aim of our study is to compare in patients with a secondary Dupuytren’s contracture the effect of a new percutaneous and lipofilling technique with standard fasciectomy surgery on convalescence, contracture correction and recurrence rate. We will use the VAS and DASH score and hand function test to measure the recovery of the hand function. This study may provide an insight into a better treatment option for patients with Dupuytren’s contractures and it may lower the costs of treatment by shortening the convalescence.
1. Townley, W.A., et al., Dupuytren's contracture unfolded. Bmj, 2006. 332(7538): p. 397-400.
2. Thurston, A.J., Dupuytren's disease. J Bone Joint Surg Br, 2003. 85(4): p. 469-77.
3. McFarlane, R., D.A. McGrouther, and M.H. Flint, eds. Dupuytren's Disease. 1990, Churchill Livingstone: Edinburgh.
Study objective
The percutaneous and lipofilling technique has a shorter convalescence.
Study design
1. Pre operative: range of motion, VAS, DASH, Semmes & Weinstein, diary, pictures, volume measure, grip force;
2. 2 weeks post operative: range of motion, VAS, Semmes & Weinstein, diary, pictures;
3. 3 weeks post operative: range of motion, VAS, Semmes & Weinstein, diary, volume measure, grip force;
4. 6 months post operative: range of motion, VAS, DASH, Semmes & Weinstein, patient satisfaction, diary, pictures;
5. 1 year post operative: range of motion, VAS, patient satisfaction.
Intervention
1. Intervention: Percutaneous lipofilling technique;
2. Control: (Dermo) fasciectomy surgery.
S.E.R. Hovius
Erasmus Medical Center
Department of Plastic Surgery and Hand Surgery
Room HS 505
Rotterdam 3000 CA
The Netherlands
+31 (0)10 703 3407
s.e.r.hovius@erasmusmc.nl
S.E.R. Hovius
Erasmus Medical Center
Department of Plastic Surgery and Hand Surgery
Room HS 505
Rotterdam 3000 CA
The Netherlands
+31 (0)10 703 3407
s.e.r.hovius@erasmusmc.nl
Inclusion criteria
1. Males and females;
2. Age;
3. Secondary Dupuytren's contracture;
4. PIP> 30º / MCP > 20º;
5. One or more affected diatheses;
6. ASA criteria I, II, and III.
Exclusion criteria
1. > 2 times surgery on affected ray;
2. congenital/trauma in past that affects the affected ray in a way that there is no 0 value;
3. Use of blood thinners that can not be stopped for surgery;
4. ASA IV and V;
5. severe CRPS in the past.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL2098 |
NTR-old | NTR2215 |
Other | Erasmus MC, Rotterdam : MEC 2009-437 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |