Endoscopic Flexor Hallucis Longus Transfer vs Minimally Invasive Repair in Acute Achilles Tendon Rupture

Sponsor
Aristotle University Of Thessaloniki (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT06114368
Collaborator
General Hospital of Naoussa (Other), Private Orthopedics Practice P. Symeonidis (Other)
40
1
30.9
1.3

Study Details

Study Description

Brief Summary

The goal of this observational study is to compare the outcomes of two different surgical techniques (Endoscopic Flexor Hallucis Longus transfer - Group 1 vs Minimally Invasive primary repair - Group 2) for patients with acute Achilles tendon rupture. The main questions to be answered are:

  1. Which group's patients are more satisfied?

  2. Which group's patients appear to have a greater complication rate?

  3. Which group's patients have greater calf and ankle circumference compared to the unaffected limb?

  4. Which group's patients have greater passive and active range of ankle motion compared to the unaffected limb?

  5. Are group 1 patients characterized by strength deficit in hallux flexion power?

Condition or Disease Intervention/Treatment Phase
  • Procedure: Surgery for the treatment of Acute Achilles tendon rupture

Detailed Description

Two separate foot and ankle surgeons in Northern Greece prefer to use a different surgical technique in their respective patients with Acute Achilles tendon rupture.

The first one (A.E.) prefers to perform only Endoscopic Flexor Hallucis Longus transfer, while the second one (P.S.) prefers to perform only Minimally invasive primary repair assisted by the Achillon device (Percutaneous Achilles Repair System - PARS). They both agreed to enroll their recently operated patients (last 5 years) in this retrospective study, which will be conducted by the researcher (M.K.). The patient's study may be retrospective, nevertheless, the patients were randomly chosen and enrolled by a prospectively designed study protocol. Each surgeon applied the respective surgical treatment modality regardless of each patient's characteristics, biometrics, or comorbidities. Inclusion and Elimination criteria will be applied. The patient's satisfaction will be evaluated with the Achilles Tendon Total Rupture Score (ATRS). Complications will be documented. Calf and ankle circumference will be measured and compared to the contralateral healthy limb. Ankle passive and active range of motion will be measured and compared to the contralateral healthy limb. Possible correlations will be investigated regarding patient age, BMI, history of smoking, level of activity, and comorbidities.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Outcomes Evaluation of Endoscopic Flexor Hallucis Longus Transfer Versus Minimally Invasive Primary Repair in Patients With Acute Achilles Tendon Rupture
Actual Study Start Date :
Mar 5, 2023
Anticipated Primary Completion Date :
Sep 30, 2024
Anticipated Study Completion Date :
Sep 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Endoscopic Flexor Hallucis Longus transfer / Group 1

Patients with acute Achilles tendon rupture managed with Endoscopic Flexor Hallucis Longus transfer by one surgeon (A.E.) in one hospital (General Hospital of Naoussa, Naoussa, Greece), all of which followed the same rehabilitation protocol.

Procedure: Surgery for the treatment of Acute Achilles tendon rupture
Two different surgical techniques were applied in two different patient groups for the same disease. Their outcomes are evaluated and compared

Minimally Invasive Primary repair / Group 2

Patients with acute Achilles tendon rupture managed with Minimally Invasive Primary repair by one surgeon (P.S.) in one hospital (St. Luke's Hospital, Thessaloniki, Greece), all of which followed the same rehabilitation protocol.

Procedure: Surgery for the treatment of Acute Achilles tendon rupture
Two different surgical techniques were applied in two different patient groups for the same disease. Their outcomes are evaluated and compared

Outcome Measures

Primary Outcome Measures

  1. Patient Satisfaction assessed with the Achilles Tendon Total Rupture Score [More than 12 months postoperatively]

    Evaluated and quantified with the Achilles Tendon Total Rupture Score (minimum value = 0 - worst outcome, maximal value = 100 - best outcome)

Secondary Outcome Measures

  1. Complication Rate [More than 12 months postoperatively]

    Complications will be recorded and categorized: Rerupture, Infection, Nerve injury, Miscellaneous

  2. Calf Circumference [More than 12 months postoperatively]

    Calf circumference measured 15 cm distally to the inferior pole of the patella. Contralateral limb calf circumference will also be measured. The Calf Circumference Difference will be calculated and compared between the two groups.

  3. Ankle Circumference [More than 12 months postoperatively]

    Ankle circumference measured 8 cm proximally to the lateral malleolus. Contralateral limb ankle circumference will also be measured. The Ankle Circumference Difference will be calculated and compared between the two groups.

  4. Ankle joint Range of Motion [More than 12 months postoperatively]

    Active and Passive Ankle joint Range of Motion will be calculated with an electronic goniometer. Contralateral limb Range of Ankle joint Motion will also be measured. The Range of Motion Difference will be calculated and compared between the two groups.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Signed Consent Form

  • Age between 18-75 years

  • Acute Achilles Tendon Rupture (<3 weeks)

  • Surgical Management with Endoscopic Flexor Hallucis Longus transfer or Minimally Invasive primary tendon repair

  • More than 12 months postoperative follow-up

  • Patients operated after 2015

Exclusion Criteria:
  • Inability or Unwillingness to cooperate

  • Medically unfit for examination (e.g. due to terminal illness)

  • Age less than 18 or more than 75 years

  • Non-operative Management as definitive treatment

  • Surgical Management other than the ones described in the inclusion criteria

  • Neglected Achilles Tendon Rupture (>3 weeks)

  • Bilateral Achilles Tendon Rupture

  • Patients operated before 2015

  • Comorbidities interfering with the secondary outcomes (e.g. Venous insufficiency resulting in lower limb excessive edema interferes with ankle and calf circumference, rheumatoid arthritis and/or previous foot and ankle surgery interferes with active and passive range of motion of the ankle, etc)

Contacts and Locations

Locations

Site City State Country Postal Code
1 General Hospital of Naoussa NĂ¡ousa Central Macedonia Greece 59200

Sponsors and Collaborators

  • Aristotle University Of Thessaloniki
  • General Hospital of Naoussa
  • Private Orthopedics Practice P. Symeonidis

Investigators

  • Principal Investigator: Michail K. Kotsapas, MD, MSc, Aristotle University Of Thessaloniki

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michail Kotsapas, Michail Kotsapas, MD, MSc, Resident of Orthopedics (General Hospital of Naoussa), PhD Candidate (Aristotle University of Thessaloniki), Aristotle University Of Thessaloniki
ClinicalTrials.gov Identifier:
NCT06114368
Other Study ID Numbers:
  • 26543
First Posted:
Nov 2, 2023
Last Update Posted:
Nov 7, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Michail Kotsapas, Michail Kotsapas, MD, MSc, Resident of Orthopedics (General Hospital of Naoussa), PhD Candidate (Aristotle University of Thessaloniki), Aristotle University Of Thessaloniki
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 7, 2023