The study is designed to evaluate the effectiveness of conservative treatment in reducing complications when treating acute Achilles tendon rupture.
ID
Bron
Verkorte titel
Aandoening
Acute Achilles tendon rupture
Ondersteuning
Divisie Heelkunde
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Complications of treatment.
Achtergrond van het onderzoek
Background:
We present the design of an open randomized multi-centre study on surgical versus conservative treatment of acute Achilles tendon ruptures. The study is designed to evaluate the effectiveness of conservative treatment in reducing complications when treating acute Achilles tendon rupture.<
Methods/Design:
At least 72 patients with acute Achilles tendon rupture will be randomized to minimally invasive surgical repair followed by functional rehabilitation using tape bandage or conservative treatment followed by functional rehabilitation with use of a functional bracing system. Both treatment arms use a 7 weeks post-rupture rehabilitation protocol. Four hospitals in the Netherlands will participate. Primary end-point will be reduction in complications other than re-rupture, notably infection, disturbed wound healing and disturbed sensibility in the sural nerve area, adhesions and thrombosis. Secondary end-point will be re-rupturing, time off work, sporting activity post rupture and patient satisfaction. Patient follow-up will be 12 month.
Doel van het onderzoek
The study is designed to evaluate the effectiveness of conservative treatment in reducing complications when treating acute Achilles tendon rupture.
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
Patients with acute Achilles tendon rupture will be randomized to minimally invasive surgical repair followed by functional rehabilitation using tape bandage or conservative treatment followed by functional rehabilitation with use of a functional bracing system.
Publiek
R. Metz
Utrecht 3582 KE
The Netherlands
+31 (0)30 2566024
metz_r@hotmail.com
Wetenschappelijk
R. Metz
Utrecht 3582 KE
The Netherlands
+31 (0)30 2566024
metz_r@hotmail.com
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Primary spontaneous Achilles tendon rupture;
2. Treatment starts within 72 hours after rupture;
3. Diagnoses by physical examination: palpable gap and calf muscle squeeze test positive for tendon rupture;
4. Age 18-65 years;
5. Informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Re-rupture / bilateral rupture / open rupture;
2. Combination with fracture of foot or ankle;
3. Former application (injection) of local corticosteroids in tendon area;
4. Contra-indications for surgery;
5. Physical or mental handicaps that do not allow functional treatment or otherwise interfere with the ability to follow-up on the study protocol.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
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Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL720 |
NTR-old | NTR730 |
Ander register | : N/A |
ISRCTN | ISRCTN50141196 |