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Clinical research on perioperative intervention of ankle fracture patients based on modified external application of ancient formula Caowu powder

Clinical research on perioperative intervention of ankle fracture patients based on modified external application of ancient formula Caowu powder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001251
Enrollment
Unknown
Registered
2025-06-23
Start date
2023-07-10
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Ankle Fracture

Interventions

control group:
Treatment group:Conventional treatment combined with external application of traditional Chinese medicine

Sponsors

Chongqing Fourth People's Hospital(Chongqing Emergency Medical Center)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for ankle fracture is a patient with unilateral ankle fracture without other injuries and has surgical indications evaluated by the surgeon. 2. The patient's age is between 18-70 years old. 3. No other related treatments were performed before treatment. 4. Voluntarily participate in this clinical study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: Patients with open fractures skin damage or local soft tissue complications (infection tension blisters necrosis compartment syndrome); Individuals with contralateral lower limb injury or limb absence; Patients with multiple injuries; In addition to ankle joint fractures there are also critically ill patients with important vascular nerve and organ injuries; Merge severe primary diseases such as heart liver kidney blood and hematopoietic system; Psychiatric patients; Pathological fracture; Individuals who have allergic reactions to the investigational drug; Patients with surgical contraindications or those assessed by surgeons as unsuitable for surgical treatment; Pregnant and lactating women; The researchers believe that it is not appropriate to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Swelling value of ankle joint;

Secondary

MeasureTime frame
Muscle bone ultrasound examination;Visual Analog Pain Scale (VAS);Surgical waiting time;

Contacts

Public ContactMao Tingli

Chongqing Emergency Medical Center

maotinee@126.com18223014188

Outcome results

None listed

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