Achilles Tendon Rupture Clinical Trial
Official title:
Mechanical Properties in Conservative Treated Achilles Tendon Ruptures With or Without Early Controlled Loading
The purpose of this study is to measure the mechanical properties of the tendon after conservative treated Achilles tendon ruptures with or without early controlled loading. This is done in a randomized trial and the mechanical properties are measured using roentgen stereometric analysis (RSA). The hypothesis is that early weightbearing improves mechanical properties of conservative treated Achilles tendon ruptures without causing elongation of the tendon.
Treatment of Achilles tendon ruptures includes surgical repair or immobilization in an orthosis, followed by prolonged rehabilitation. Improved rehabilitation regimens still display imperfect recovery, with deficits such as persistent end-range muscle weakness, tendon elongation and incomplete return to pre-injury activity level. The underlying mechanisms are unknown, but are likely to involve molecular and cellular aspects of the early healing processes. Animal experiments have shown that short episodes of vigorous loading during tendon healing create a stronger tendon, and lead to less elongation than continuous loading. Early controlled training has also been shown to improve the material properties of surgically repaired tendons. However, more and more clinics now turn away from surgery and towards conservative treatment, while studies on rehabilitation mainly concern sutured tendons. It is therefore also important to understand how to best rehabilitate conservatively treated patients. The aim is to investigate the effect of early controlled loading on conservatively treated Achilles tendon ruptures. The patients (age 18-60 years of age) are treated conservatively by receiving a removable foam walker boot at the emergency department. The patients are thereafter called by the principal investigator and are asked if they want to participate in the study. Patients who are interested in participating in the study receive oral and in written information about the study of the principal investigator of the study (Pernilla Eliasson). After 2 weeks, the rupture is localized by ultrasound and 4 tantalum beads are implanted percutaneously in the proximal and distal part of the tendon. These beads are used for measurements of the mechanical properties of the tendon by using RSA. The patients are thereafter randomized to early controlled loading or control. All patients wear the foam walker boot for 7 weeks. Full weight-bearing is allowed as tolerated from the beginning. Both groups perform motion exercises outside the boot with 20 repetitions, 3 times per day as of 14 days after rupture. The patients in the early loading group are provided with a special training pedal where pedal resistance can be increased during the treatment period. The patients will use this pedal twice a day starting 2 weeks after rupture. After the initial 7 weeks, the patients are referred to physical therapists uninvolved in this research, but with the instruction to follow the regional rehabilitation guidelines for Achilles tendon ruptures. Mechanical properties of the tendon will be estimated by measuring tendon length, cross-sectional area (CSA) and stiffness at week 7, 19 and 52. The elastic modulus of the tendon at 19 weeks it the primary variable of this study. At week 7, both the elastic and plastic deformation will be measured. Tendon CSA will be evaluated using computer tomography (CT). Tendon elongation will be evaluated by RSA at week 2, 7, 19 and 52. Calf muscle circumference, passive and active range of motion in the ankle joint and a heel-raise test will be performed at week 19 and 52. The overall function will be assessed by the Achilles Tendon Rupture Score at 19 and 52 weeks. Complications and re-ruptures will be registered. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00537784 -
Platelet Concentrate in Achilles Tendon Repair
|
N/A | |
Recruiting |
NCT04663542 -
The Efficacy of Different Immobilization Times After Achilles Tendon Rupture Surgery
|
N/A | |
Withdrawn |
NCT04492059 -
Use of Blood Flow Restriction Therapy in Perioperative Rehabilitation Following Achilles Tendon Rupture
|
N/A | |
Recruiting |
NCT03259204 -
Swedish Multicenter Trial of Outpatient Prevention of Leg Clots
|
N/A | |
Completed |
NCT00489749 -
A Study Comparing Protected Early Weightbearing Versus Non-Weightbearing After Surgery for Achilles Tendon Rupture
|
N/A | |
Active, not recruiting |
NCT03525964 -
Individualized Treatment of Acute Achilles Tendon Rupture
|
N/A | |
Completed |
NCT02018224 -
Achilles Tendon Rupture, Comparison Two Different Operative Techniques. Prospective Randomized Controlled Trial. 14 Years Follow-up.
|
N/A | |
Completed |
NCT04121377 -
Feasibility of an Early Progressive Strength Exercise Programme for Acute Achilles Tendon Rupture
|
N/A | |
Active, not recruiting |
NCT02318472 -
Early Mobilization After Achilles Tendon Rupture
|
N/A | |
Terminated |
NCT01237613 -
Prospective Study on Artelon® Tissue Reinforcement in Repair of Chronic Ruptures and Re-ruptures of the Achilles Tendon
|
N/A | |
Recruiting |
NCT06254794 -
Effect of BFR Rehab After Achilles Tendon Rupture
|
N/A | |
Recruiting |
NCT06009978 -
Effect of Additional Treatment With NMES After Achilles Tendon Rupture
|
N/A | |
Enrolling by invitation |
NCT05614908 -
Outcome After Conservatively Treated Achilles Tendon Rupture
|
||
Completed |
NCT03931486 -
Detection of Bacterial DNA and Collagen Metabolism in Acutely Ruptured Achilles Tendons
|
||
Recruiting |
NCT05683080 -
Impact of Achilles Tendon Rupture on the Achilles Tendon and Calf Muscles
|
||
Recruiting |
NCT05717270 -
Two-layer Suturing of Achilles Tendon Ruptures
|
||
Completed |
NCT04263493 -
Delayed Loading Following Repair of a Ruptured Achilles Tendon
|
N/A | |
Not yet recruiting |
NCT05676632 -
Impact of Achilles Tendon Ruptures: Cross-Sectional Analysis
|
||
Recruiting |
NCT04912154 -
The Efficacy of Different Rehabilitation Protocols After Achilles Tendon Rupture Surgery
|
N/A | |
Recruiting |
NCT05304819 -
PMCF Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair
|