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

NCT ID: NCT03887585

Last Updated: 2019-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-01

Study Completion Date

2020-01-01

Brief Summary

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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

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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.

Conditions

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Achilles Tendon Contracture

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Achilles tendon lengthening

Surgery of percutaneous Achilles tendon lengthening by triple hemisection

Group Type EXPERIMENTAL

Achilles tendon lengthening

Intervention Type PROCEDURE

Achilles tendon lengthening by triple hemisection for Achilles tendon contracture

Interventions

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Achilles tendon lengthening

Achilles tendon lengthening by triple hemisection for Achilles tendon contracture

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

3 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Southwest Hospital, China

OTHER

Sponsor Role lead

Responsible Party

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Xiaojun Duan

vice dean

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Xiaojun Duan, MD

Role: PRINCIPAL_INVESTIGATOR

Southwest Hospital, China

Locations

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Southwest Hospital

Chongqing, , China

Site Status

Countries

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China

Other Identifiers

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Tendon

Identifier Type: -

Identifier Source: org_study_id

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