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A comparative study for the efficacy and safety of intensive rehabilitation and conventional rehabilitation in the treatment of pelvic fractures: A multicenter prospective randomized controlled trial

Study and popularization of perioperative rehabilitation techniques for pelvic fracture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023750
Enrollment
Unknown
Registered
2019-06-10
Start date
2019-06-17
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

Pelvic and Acetabular fracture

Interventions

Control group:routine treatment
Experimental group:intensive rehabilitation techniques

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients admitted through the emergency department or transferred to our institutions who meet the following criteria will be included in the study: 1. Aged 14 to 65 years old; 2. Acute pelvic or acetabular fractures (AO classification 61 or 62).

Exclusion criteria

Exclusion criteria: Patient who meet any one or more of the following criteria will be excluded from the study: 1. Mental disorders such as dementia, cognitive disorder, etc.; 2. Multiple fractures, or multiple trauma such as head injury, spine injury, severe chest or abdominal trauma; 3. Time from injury to admission is more than 21 days.

Design outcomes

Primary

MeasureTime frame
Majeed score;Ability of daily life (Barthel index);SF-36;

Secondary

MeasureTime frame
Range of motion of hip joint;Patient satisfaction;Time of rehabilitation achievement;

Countries

China

Contacts

Public ContactWu Xinbao

Beijing Jishuitan Hospital

wuxinbao_jst@126.com+86 010-58516453

Outcome results

None listed

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