Skip to content

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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03887585
Enrollment
25
Registered
2019-03-25
Start date
2010-01-01
Completion date
2020-01-01
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Achilles Tendon Contracture

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.

Interventions

PROCEDUREAchilles tendon lengthening

Achilles tendon lengthening by triple hemisection for Achilles tendon contracture

Sponsors

Southwest Hospital, China
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 80 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Changes in the American Orthopaedic Foot & Ankle Society (AOFAS) scoresBefore surgery and up to 8 years after surgeryThe 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

MeasureTime frameDescription
Equinus recurrence rateUp to 8 years after surgeryThe equinus recurrence rate of the patients after surgery is recorded. Lower value represents a better outcome.
Infection rateUp to 8 years after surgeryThe infection rate of the patients after surgery is recorded. Lower value represents a better outcome.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026