Skip to content

A randomized controlled study comparing the effects of two types of braces on postoperative functional recovery in children with supracondylar humeral fractures: efficacy and safety evaluation at two weeks and three weeks

A randomized controlled study comparing the effects of two types of braces on postoperative functional recovery in children with supracondylar humeral fractures: efficacy and safety evaluation at two weeks and three weeks

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116239
Enrollment
Unknown
Registered
2026-01-07
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Supracondylar fracture of humerus

Interventions

Group A (Trial group):After surgery, use polymer plaster braces to fix the affected limb in a functional position for a duration of 2 weeks. Remove the brace after 2 weeks, remove the Kirschner wire a
Group B (Control group):After surgery, use polymer plaster braces to fix the affected limb in a functional position for a period of 3 weeks. Remove the brace after 3 weeks, remove the Kirschner wire a

Sponsors

The Second Affiliated Hospital of Inner Mongolia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: 1. Age under 14 years old; 2. Diagnosed by imaging as Gartland type II and III extension type humeral epicondylar fractures; 3. Within 7 days after injury, undergo closed reduction and percutaneous needle fixation surgery at our hospital; 4. The legal guardian of the patient signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pathological fracture or concomitant severe fractures at other sites; 2. Open fracture or concomitant significant nerve or vascular injury; 3. History of prior surgical intervention or functional impairment on the affected elbow; 4. Presence of severe systemic medical conditions (e.g., coagulopathy, severe cardiac disease) rendering the patient unfit for surgery; 5. Patients unlikely to complete the required follow-up schedule.

Design outcomes

Primary

MeasureTime frame
Flynn Elbow Function Rating Criteria at 12 Weeks Postoperatively;

Secondary

MeasureTime frame
Range of motion of elbow joint;Complication rates included malunion (Baumann angle change >12°), re-fracture, pin tract infection, iatrogenic nerve injury, and heterotopic ossification.;Baumann;Carrying angle;Lateral humeral head angle;

Countries

China

Contacts

Public ContactBai Rui

The Second Affiliated Hospital of Inner Mongolia Medical University

bairuiandaiqing@126.com+86 176 1481 0000

Outcome results

None listed

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