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Achilles Tendon Rupture clinical trials

View clinical trials related to Achilles Tendon Rupture.

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NCT ID: NCT01622179 Unknown status - Clinical trials for Achilles Tendon Rupture

Outcome of Two Different Suture Methods for Achilles Tendon Rupture

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to estimate the effective of two suture methods in the treatment of Achilles rupture.

NCT ID: NCT01298024 Completed - Clinical trials for Achilles Tendon Rupture

A Pilot Study on Exercise After Achilles Tendon Rupture

NEMEX-ATR
Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose is to study the effect of early NEuroMuscular EXercise (NEMEX) versus conventional treatment (late exercise) in patients with acute non-operative achilles tendon rupture (ATR).

NCT ID: NCT01265004 Completed - Microcirculation Clinical Trials

Identification of Microcirculation After Surgical Treatment of Rupture of the Achilles Tendon

MicroASR
Start date: December 2010
Phase: N/A
Study type: Observational

This project investigates microcirculation in skin and tendon after a rupture of the Achilles tendon. Three different treatments are compared: stitches of the tendon, fibrin-glue and the combination of both.

NCT ID: NCT01237613 Terminated - Clinical trials for Achilles Tendon Rupture

Prospective Study on Artelon® Tissue Reinforcement in Repair of Chronic Ruptures and Re-ruptures of the Achilles Tendon

Start date: November 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the surgical and clinical outcome of Artelon® Tissue Reinforcement in repair of chronic ruptures or re-ruptures of the Achilles tendon, with regard to lower leg and foot function, pain and quality of life.

NCT ID: NCT01063465 Recruiting - Clinical trials for Achilles Tendon Rupture

Measurement of Mechanical Properties of the Healing Achilles Tendon With or Without Early Weightbearing

Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to measure the mechanical properties of healing Achilles tendons in humans after early controlled weightbearing, compared with a control group in a randomized, single-blinded trial. The mechanical properties are measured using radiostereophotogrammetic x-rays (RSA). Hypothesis: Early weightbearing improves mechanical properties of the healing Achilles tendon.

NCT ID: NCT00537784 Completed - Clinical trials for Achilles Tendon Rupture

Platelet Concentrate in Achilles Tendon Repair

Start date: September 2007
Phase: N/A
Study type: Interventional

People operated for a rupture of the Achilles tendon receive a concentrate of their own platelets injected into the operated area. The study is randomized and single-blinded, with 20 treated patients and 20 controls, who get no injection. The primary endpoint is a mechanical property of the tendon after 12 weeks (modulus of elasticity), as measured by a special type of radiography. This radiography uses 0.8 mm metal markers, which are injected into the tendon. The tendon is mechanically loaded during radiography and its strain can be measured as increased distance between the markers. Other mechanical variables at 6, 12 and 52 weeks are secondary variables, as well as a validated patient-administrated questionaire at 1 year.

NCT ID: NCT00489749 Completed - Clinical trials for Achilles Tendon Rupture

A Study Comparing Protected Early Weightbearing Versus Non-Weightbearing After Surgery for Achilles Tendon Rupture

Start date: October 2003
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the effect of protected early weightbearing (PEWB) compared to non-weightbearing (NWB) after surgery for an Achilles tendon rupture (ATR) on health related quality of life (HRQL) in the initial six week period after surgery, functional recovery over time, return to work and activity and complications. We hypothesized that PEWB following ATR repair would result in: i) improved HRQL in the initial postoperative period, ii), a quicker recovery of HRQL, strength and endurance, iii) earlier return to work and sport, and iv) no increase in complications, such as re-rupture compared to NWB.

NCT ID: NCT00284648 Completed - Clinical trials for Achilles Tendon Rupture

Operative Versus Non-operative Treatment of Achilles Tendon Rupture

Start date: December 2000
Phase: N/A
Study type: Interventional

This study is intended to determine whether the optimal treatment of acute Achilles tendon ruptures is surgical repair or functional bracing. Our hypotheses are surgical repair will: 1) Result in a clinically relevant decrease in re-rupture rate and 2) Result in a clinically relevant improvement in disease specific quality of life and 3) A clinically relevant improvement in functional outcome measures