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Clinical Trials/NCT03887585
NCT03887585
Unknown
Not Applicable

Modified Percutaneous Achilles Tendon Lengthening by Triple Hemisection for Achilles Tendon Contracture

Southwest Hospital, China1 site in 1 country25 target enrollmentJanuary 1, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Achilles Tendon Contracture
Sponsor
Southwest Hospital, China
Enrollment
25
Locations
1
Primary Endpoint
Changes in the American Orthopaedic Foot & Ankle Society (AOFAS) scores
Last Updated
7 years ago

Overview

Brief Summary

This study aims to evaluate the efficacy and safety of this new therapeutic method, which is based on the percutaneous sliding technique with three hemi-cuts in the tendon.

Detailed Description

This study aims to provide a new therapeutic theory which bases on the percutaneous sliding technique with three hemi-cuts in the tendon. In this study, Achilles tendon parenchymal at distal level is hemisected through the most distal incision, Achilles tendon parenchymal at proximal level is hemisected through the middle incision, then Achilles tendon lengthening is accomplished by the sliding tendon under forceful dorsiflexion. It can better achieve soft tissue balance and reduce the recurrence of Achilles tendon contracture when Achilles tendon strength in plantarflexion is weakened. Thus in this study, the partial aponeurosis of gastrocnemius is cut off at most proximal incision in order to weaken Achilles tendon strength in plantarflexion.

Registry
clinicaltrials.gov
Start Date
January 1, 2010
End Date
January 1, 2020
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Southwest Hospital, China
Responsible Party
Principal Investigator
Principal Investigator

Xiaojun Duan

vice dean

Southwest Hospital, China

Eligibility Criteria

Inclusion Criteria

  • Patients older than three years old;
  • Severe Achilles tendon contracture and equinus;
  • The time after Achilles tendon contracture more than 6 months ;
  • Initial Achilles tendon lengthening.

Exclusion Criteria

  • Patients younger than 3 years;
  • The course of Achilles tendon contracture is within 6 months;
  • Patients who have suffered from the Achilles tendon lengthening;
  • Obvious contracture of other soft tissues occurs in combination, such as compartment syndrome or extensive scar tissues in calf;
  • Osteotomy or tendon transposition is needed.
  • Ankle joint is damaged obviously, such as Charcot's joint or Hemophilic arthritis;
  • Skin soft-tissue infection in the lower limb.
  • Initial Achilles tendon lengthening.

Outcomes

Primary Outcomes

Changes in the American Orthopaedic Foot & Ankle Society (AOFAS) scores

Time Frame: Before surgery and up to 8 years after surgery

The AOFAS scores of the patients before and after surgery are recorded. The scale ranges from 0-100 points, and increases of the value represent a better outcome.

Secondary Outcomes

  • Equinus recurrence rate(Up to 8 years after surgery)
  • Infection rate(Up to 8 years after surgery)

Study Sites (1)

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