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Clinical study of new prothesis for distal humeral surface replacement

Clinical study of new prothesis for distal humeral surface replacement

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035823
Enrollment
Unknown
Registered
2020-08-18
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

elbow stiffness

Interventions

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Patient aged between 12 to 65 years, and can cooperate with postoperative exercises; 2. Patients with distal humeral articular surface destruction and joint deformity; 3. Can cooperate with long-term clinical follow-up.

Exclusion criteria

Exclusion criteria: 1. The affected limb has wrist joint dysfunction or ulnar and radial shaft malunion and other diseases that affect the forearm rotation function; 2. Mental disorders; 3. Other cases in which the patients could not cooperate with the treatment; 4. Patients with severe diabetes mellitus, liver and kidney dysfunction, severe osteoporosis, organic heart disease and arrhythmia, women with positive pregnancy test or lactation, men and women with short-term family planning, and patients with history of allergy to nonsteroidal anti-inflammatory drugs or cyclic methionine.

Design outcomes

Primary

MeasureTime frame
ROM of elbow;pain score;functional score of elbow;

Secondary

MeasureTime frame
blood loss of elbow;inflammatory indicators;

Countries

China

Contacts

Public ContactFan Cunyi

Shanghai Sixth People's Hospital

fancunyi888@163.com+86 18930177799

Outcome results

None listed

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