Clinical analysis of tension-free beam suture for the treatment of acute closed Achilles tendon rupture

Clinical and biomechanical study of tension-free beam suture for the treatment of acute closed Achilles tendon rupture

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000030637

Enrollment

Unknown

Registered

2020-03-08

Start date

2020-04-01

Completion date

Unknown

Last updated

2020-08-24

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

Conditions

Acute closed Achilles tendon rupture

Interventions

experimental group:tension-free beam suture technique

control group:traditional suture technique

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. With acute Achilles tendon rupture, <= 2 weeks duration; 2. With closed Achilles tendon rupture; 3. Achilles tendon rupture is located 2-8cm above the calcaneal tubercle; 4. Patients who are able to understand and support the research process, volunteer to participate in project research, and sign informed consent. And compliance is good, and can be followed up with patients for at least 1 year.

Exclusion criteria

Exclusion criteria: 1. With avulsion of Achilles tendon avulsion fracture and other parts combined injury; 2. With previous chronic Achilles tendinitis; 3. With previous medical history of local injection or oral steroid hormones; 4. Mental patients without self-awareness.

Design outcomes

Primary

Measure	Time frame
the Achilles tendon Total Rupture Score;	—

Countries

China

Contacts

Public ContactYunfeng Yang

Department of Orthopedics, Shanghai Tongji Hospital

yyfscn@163.com+86 13918588939

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026