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Two-layer Suturing of Achilles Tendon Ruptures

Two-layer Suturing of Achilles Tendon Ruptures - an Ambidirectional Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05717270
Acronym
ATRBFH
Enrollment
23
Registered
2023-02-08
Start date
2023-05-23
Completion date
2026-02-01
Last updated
2024-09-27

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 purpose of the present study is to measure whether a new technique of double row suturing of a ruptured Achilles tendon will result in a normalization of the length of the Soleus part (primary outcome) and of the superficial Gastrocnemius part of the tendon (secondary outcome) one-week post-operative. Results will be compared to that of a participants group that underwent the same operation but with a standard operative technique and the same rehabilitation regime recently completed (NCT04263493). The investigators hypothesize that the new suturing technique will result in an elongation of the Soleus part of the Achilles tendon (primary outcome) by 8.9 mm or less relative to the uninjured contralateral side one week (primary endpoint) after surgery compared to retrospective data from a recently completed randomized controlled trial

Detailed description

This study is an ambidirectional cohort study with a retrospective part based on a recently completed trial (NCT04263493) and this prospective registered trial.

Interventions

PROCEDURETwo-layered suture repair

The ruptured Achilles tendon will be sutured in two-layer.

Sponsors

Bispebjerg Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed with a traumatic, complete mid-substance Achilles tendon rupture * Manages transportation to/from the hospital on their own * Presented within 14 days from injury * Adult (18 to 60 years) * Understands Danish

Exclusion criteria

* Other injuries affecting their lower limb functions * Prior Achilles contralateral tendon rupture * Contraindications for MRI * Re-rupture * Smoking * Systemic diseases influencing tendon healing * Anticoagulation treatment * Inability to follow rehabilitation or complete follow-ups * Immunosuppressive treatment including systemic corticosteroid treatment.

Design outcomes

Primary

MeasureTime frameDescription
Tendon lengthOne week after surgery.The distance between the distal muscle fibers of the Soleus muscle and the posterior most superior part of the calcaneus.

Secondary

MeasureTime frameDescription
Tendon length Triceps Surae6 months.The soleus and gastrocnemius tendon length (mm).
Plantar flexion function6 and 12 months.Heel-rise test
Patient perception12 monthsAchilles Tendon Total Rupture Score (ATRS). The ATRS consist of 10 items, with a total score range from 0 to 100, and a low score indicate more limitations in physical activity and worse symptoms.
Tendon length SoleusOne week after surgery.The distance (mm) between the distal muscle fibers of the gastrocnemius muscle and the posterior most superior part of the calcaneus.
Muscle architecture fascicle length6 months.Gastrocnemius and soleus muscle fascicle length (mm).
Muscle architecture pennation angle6 months.Gastrocnemius and soleus muscle pennation angle (°).
Muscle cross sectional area6 months.Gastrocnemius and soleus tendon and lower limb muscle cross-sectional area (mm2).
Vascularisation6 months.Doppler flow (area in mm2)

Countries

Denmark

Outcome results

None listed

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