Actively Recruiting

Age: 7Years +
All Genders
ID07338110

Prospective Cohort Study of Patients Undergoing Surgical Repair of the Achilles Tendon

Led by Chirurgie Du Sport · Updated on 2026-03-19

5000

Participants Needed

1

Research Sites

1043 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to better understand the long-term outcomes of patients who have undergone surgery to repair Achilles tendon injuries. The study follows these patients over a 20-year period to evaluate the rates of tendon re-rupture, the quality and frequency of return to sports, and any complications related to the surgical procedures. The goal is to gather detailed information to improve knowledge about the durability and clinical effectiveness of Achilles tendon repair techniques. The study focuses on patients who have had Achilles tendon surgery, which may include direct tendon repair for acute ruptures or more complex reconstruction techniques for chronic or severe cases. These surgical methods can involve tendon transfers or grafts to restore tendon function and strength. The study observes patients over two decades, collecting data on their recovery and function after surgery. Participants will be monitored for 20 years following their surgery. During this time, researchers will assess re-rupture incidents, evaluate return to sport using various activity and functional scoring systems, and track complications. Tools such as the Visual Analogue Scale, Achilles Tendon Total Rupture Score, and activity scales like UCLA and Tegner are used to measure long-term function. This extensive follow-up aims to provide valuable insight into the lasting effects of Achilles tendon repair.

CONDITIONS

Brief Title

French Achilles Tendon Surgery Cohort Study

Who Can Participate

Age: 7Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing Achilles tendon repair surgery
Not Eligible

You will not qualify if you...

  • Patient refusal

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Hospital stay duration as per routine surgical care

Participants undergo Achilles tendon repair surgery and receive immediate post-operative care to restore tendon function.

1 surgery visit and several immediate post-operative visits

Long-term Monitoring

Duration - Up to 20 years

Participants are followed for up to 20 years to assess re-rupture rates, return to sport, functional outcomes, and complications after Achilles tendon surgery.

Regular follow-up visits over 20 years depending on study schedule

Trial Site Locations

Total: 1 location

1

Chirurgie du Sport

Paris, Île-de-France Region, France, 75005

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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