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A randomized, double blind, placebo controlled, multi-center clinical study to evaluate the recovery of wrist joint function after the treatment of distal radius fractures with white vein ointment

A randomized, double blind, placebo controlled, multi-center clinical study to evaluate the recovery of wrist joint function after the treatment of distal radius fractures with white vein ointment

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16009866
Enrollment
Unknown
Registered
2016-11-15
Start date
2016-11-14
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Fracture of distal radius

Interventions

treatment group:Baimai ointment
control group:placebo

Sponsors

Beijing Ji Shui Tan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for distal radius fractures; 2. Closed fracture; 3. Using the treatment of Open reduction and plate internal fixation; 4. Imaging studies have shown that anatomical reduction or functional restoration; 5. No initial infection or has been effectively controlle; 6. Aged 35-70 years old; 7. Patients who volunteered to participate this study himseif, and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with distal radius fractures treated with none operative treatment; 2. Patients with distal radius fractures and other parts of the fracture; 3. Patients with skin disease around the wound; 4. Patients with open fractures of the distal radius; 5. Patients with a severe medical illness; 6. Allergic constitution (Patients who are allergic to more than two kinds of food, drugs, pollen and others ) Or Patients who are allergic to known components of the test drug; 7. A woman who is pregnant or is preparing for pregnancy; 8. Patients with mental disorders or disturbances of consciousness which will make it is difficult to assess the effectiveness and safety of drugs; 9. Patients used to participate in other clinical trials in last 3 months or patients are participating in other clinical trials in or about 3 months; 10. Patients are considered to be unsuitable for this study by researchers.

Design outcomes

Primary

MeasureTime frame
Degree of joint pain;The swelling of the wrist;Cooney score;PRWE score;

Secondary

MeasureTime frame
Hand swelling;Wrist activity;Grip;

Countries

China

Contacts

Public ContactMAOQI GONG

Beijing Ji Shui Tan Hospital

13264239959@163.com+86 010 58516688

Outcome results

None listed

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