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A Randomized Controlled, Group-Sequential Clinical Trial on the Efficacy of Pulse Electromagnetic Field (PEMF) Therapy Device in Treating Fresh Distal Radius Fractures

A Randomized Controlled, Group-Sequential Clinical Trial on the Efficacy of Pulse Electromagnetic Field (PEMF) Therapy Device in Treating Fresh Distal Radius Fractures

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125886
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Closed fracture of the distal radius

Interventions

Intervention group:Standard conventional treatment plus bone trauma therapeutic apparatus (once daily for 6 hours per session)

Sponsors

Second Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Closed distal radius fracture. 2.Received reduction and internal fixation. 3.Aged 18 to 65 years (inclusive). 4.The patient agrees to participate and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Pathological fracture or old fracture. 2.Severe multiple trauma, history of or current malignant tumor, compartment syndrome. 3.Known history of endocrine or metabolic disorders affecting bone formation. 4.Systemic use of corticosteroids, use of growth factors, use of chemotherapeutic drugs, or local radiotherapy. 5.Pregnant or lactating women, or those planning pregnancy during the trial period. 6.Long-term use of sedative-hypnotics or long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) for more than 3 consecutive months. 7. Mental illness, substance abuse, or alcoholism. 8.Severe diseases of the heart, liver, kidney, lung, blood system, or other metabolic diseases. 9.Any other conditions deemed by the investigator to make the patient unsuitable for participation in this study. 10.Patients admitted to hospital =10 days after fracture. 11.Carrying any life-sustaining electronic devices.

Design outcomes

Primary

MeasureTime frame
Percentage of fracture healing;

Countries

China

Contacts

Public ContactTan Yanbin

Second Affiliated Hospital of Zhejiang University School of Medicine

drtany@hotmail.com+86 135 8816 9527

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026