Skip to content

Periosteal bone graft versus osteochondral graft in the treatment of osteochondral lesions of the talus: a multicenter, randomized controlled, non-inferior study

Periosteal bone graft versus osteochondral graft in the treatment of osteochondral lesions of the talus: a multicenter, randomized controlled, non-inferior study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084540
Enrollment
Unknown
Registered
2024-05-20
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Osteochondral Lesions of the Talus

Interventions

Control group:osteochondral transplantation
Test group:periosteal bone transplantation

Sponsors

Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who meet all of the following criteria are considered eligible for inclusion A. Age 18-60 years old, male or female; B. Clinical examination and imaging examination confirmed talus cartilage injury with ankle pain, which was ineffective after conservative treatment for more than 3 months; C. Preoperative magnetic resonance evaluation suggested that the damage range of talus cartilage was greater than 100mm2; D. The patient intends to undergo open surgical treatment; E. The patient is willing and able to comply with the planning, rehabilitation, care, and follow-up protocols of the study.

Exclusion criteria

Exclusion criteria: Subjects meeting any of the following criteria will not be admitted to the trial A. A history of previous surgery on the affected ankle; B. Combined with degree III or above ankle ligament injury; C. Patients with ankle osteoarthritis or traumatic arthritis; D. Have diabetes or neurological disease; E. Has an autoimmune disease and is active; F. mental abnormality or any mental abnormality affecting the patient's behavior.

Design outcomes

Primary

MeasureTime frame
AOFAS score 1 year after surgery;The incidence of complications in the bone extraction area 1 year after surgery;

Secondary

MeasureTime frame
AOFAS score 3 months, 6 months, 24 months after surgery;Pain VAS 3 months, 6 months, 12 months, 24 months after surgery;MOCART 2.0 MR Score 6 months, 12 months, 24 months after surgery;Tegner score 3 months, 6 months, 12 months, 24 months after surgery;

Countries

China

Contacts

Public ContactSong Weidong

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

songsz999@163.com+86 137 1066 6839

Outcome results

None listed

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