Skip to content

Endoscopic Transfer of Flexor Hallucis Longus Tendon for Chronic Achilles Tendon Rupture

Endoscopic Assisted Transfer of Flexor Hallucis Longus Tendon for Chronic Achilles Tendon Rupture. A Prospective Multi Center Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02996253
Enrollment
38
Registered
2016-12-19
Start date
2015-12-31
Completion date
2024-02-29
Last updated
2023-03-22

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

Conditions

Achilles Tendon Rupture

Brief summary

The transfer of Flexor Hallucis Longus (FHL) in the management of chronic Achilles tendon ruptures has demonstrated good functional outcome, but an extensive surgical field at a vulnerable location may lead to increased risk for soft tissue problems. The arthroscopic FHL transfer may reduce the risk for soft tissue problems. Functional outcome parameters are investigated, wound/soft tissue complications registered.

Detailed description

The transfer of FHL in the management of chronic Achilles tendon ruptures has demonstrated good functional outcome with American Orthopaedic Foot ane Ankle Society (AOFAS) hindfoot scores at 80-89. The extensive surgical field by either a two-incision approach or a single longitudinal posterior approach to the Achilles tendon may lead to an increased risk for soft tissue problems, both infections and wound healing problems. The endoscopic FHL transfer may reduce the risk for soft tissue problems while retaining a good functional outcome. Several functional outcome measures and scores are evaluated a year after surgery. Prospective study for evaluation of the surgical procedure.

Interventions

PROCEDUREFHL transfer

endoscopic transfer og flexor hallucis longus

Sponsors

Central Hospital, Fredrikstad
CollaboratorUNKNOWN
Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Chronic Achilles Tendon Rupture

Exclusion criteria

* Pregnancy * BMI\<18.5 or \>39.9 * Insufficient Norwegian Language proficiency lack of communication skills local skin conditions at site for planned surgery

Design outcomes

Primary

MeasureTime frame
The Victorian Institute of Sports Assessment- Achilles Questionnaire (VISA-A) outcome scoreone year after FHL transfer

Secondary

MeasureTime frameDescription
patient reported function score (PRFS)6, 12 monthspatient reported Activity related disability
Magnetic resonance imagine (MRI)one year post surgeryFHL hypertrophy
functional test battery12 monthsjump- and strength tests
Visual Analogue Scale for Pain (VAS pain) score3, 6 and 12 months after FHL transferpatient reported outcome
AOFAS hindfoot3,6,12 months
VISA-A6 months after surgery
local wound conditionswithin 12 weekswound infection

Countries

Norway

Outcome results

None listed

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