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Conservative treatment and rehabilitation of acute ankle sprain

Conservative treatment and rehabilitation of acute ankle sprain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113133
Enrollment
Unknown
Registered
2025-11-25
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

acute ankle sprain

Interventions

Observation group:None

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients diagnosed with acute ankle sprain; (2) Unilateral ankle sprain; (3) Patients aged between 10 and 75 years; (4) The time from injury to first medical treatment was not more than 3 days; (5) There were complete follow-up data and rehabilitation training records.

Exclusion criteria

Exclusion criteria: (1) Patients with suspected fracture according to the Ottawa Ankle Rules (OAR) and/or X-ray examination; (2) A history of ankle sprain; (3) Patients with more urgent or serious conditions than ankle sprain requiring treatment; (4) The investigator considered that the patient suffered from symptoms that were not suitable for participating in clinical research; (5) Combined with other severe lower limb injuries (such as femoral shaft fracture, knee joint injury) or severe chronic diseases (such as uncontrolled diabetes, chronic heart failure); (6) The patient is currently receiving treatment for complications that the investigator considers inappropriate; (7) Patients with a physical or mental disorder that would affect their voluntary participation in the trial (e.g., dementia, severe mental illness, severe visual or hearing impairment, illiteracy, drug addiction); (8) Patients unable to participate in the study due to time or distance constraints; (9) Patients with incomplete rehabilitation records or less than 6 months of follow-up.

Design outcomes

Primary

MeasureTime frame
FAOS score;

Secondary

MeasureTime frame
AOFAS score;VAS score;ankle range of motion;Incidence of Complications;SF-36 score;Compliance with rehabilitation;

Countries

China

Contacts

Public ContactZhongmin Shi

Shanghai Sixth People's Hospital

szm1972@sjtu.edu.cn+86 189 3017 7323

Outcome results

None listed

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