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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05717270
Other study ID # ATR_sutur_BFH
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 23, 2023
Est. completion date February 1, 2026

Study information

Verified date August 2023
Source Bispebjerg Hospital
Contact Anne-Sofie Agergaard, Postdoc
Phone 004529928343
Email anne-sofie.agergaard@regionh.dk
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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


Description:

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


Recruitment information / eligibility

Status Recruiting
Enrollment 23
Est. completion date February 1, 2026
Est. primary completion date February 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Two-layered suture repair
The ruptured Achilles tendon will be sutured in two-layer.

Locations

Country Name City State
Denmark Institute of Sports Medicine Copenhagen Copenhagen NV

Sponsors (1)

Lead Sponsor Collaborator
Bispebjerg Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tendon length The distance between the distal muscle fibers of the Soleus muscle and the posterior most superior part of the calcaneus. One week after surgery.
Secondary Tendon length Soleus The distance (mm) between the distal muscle fibers of the gastrocnemius muscle and the posterior most superior part of the calcaneus. One week after surgery.
Secondary Tendon length Triceps Surae The soleus and gastrocnemius tendon length (mm). 6 months.
Secondary Plantar flexion function Heel-rise test 6 and 12 months.
Secondary Patient perception Achilles 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. 12 months
Secondary Vascularisation Doppler flow (area in mm2) 6 months.
Secondary Muscle architecture fascicle length Gastrocnemius and soleus muscle fascicle length (mm). 6 months.
Secondary Muscle architecture pennation angle Gastrocnemius and soleus muscle pennation angle (°). 6 months.
Secondary Muscle cross sectional area Gastrocnemius and soleus tendon and lower limb muscle cross-sectional area (mm2). 6 months.
See also
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Completed NCT02805751 - Early Controlled Loading on Conservative Treated Achilles Tendon Ruptures N/A
Completed NCT00489749 - A Study Comparing Protected Early Weightbearing Versus Non-Weightbearing After Surgery for Achilles Tendon Rupture N/A
Active, not recruiting NCT03525964 - Individualized Treatment of Acute Achilles Tendon Rupture N/A
Completed NCT02018224 - Achilles Tendon Rupture, Comparison Two Different Operative Techniques. Prospective Randomized Controlled Trial. 14 Years Follow-up. N/A
Completed NCT04121377 - Feasibility of an Early Progressive Strength Exercise Programme for Acute Achilles Tendon Rupture N/A
Active, not recruiting NCT02318472 - Early Mobilization After Achilles Tendon Rupture N/A
Terminated NCT01237613 - Prospective Study on Artelon® Tissue Reinforcement in Repair of Chronic Ruptures and Re-ruptures of the Achilles Tendon N/A
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Completed NCT03931486 - Detection of Bacterial DNA and Collagen Metabolism in Acutely Ruptured Achilles Tendons
Recruiting NCT05683080 - Impact of Achilles Tendon Rupture on the Achilles Tendon and Calf Muscles
Completed NCT04263493 - Delayed Loading Following Repair of a Ruptured Achilles Tendon N/A
Not yet recruiting NCT05676632 - Impact of Achilles Tendon Ruptures: Cross-Sectional Analysis
Recruiting NCT04912154 - The Efficacy of Different Rehabilitation Protocols After Achilles Tendon Rupture Surgery N/A
Recruiting NCT05304819 - PMCF Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon Repair