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Research and analysis of related factors affecting of lower limb orthopedic surgery rehabilitation

Research and analysis of related factors affecting of lower limb orthopedic surgery rehabilitation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056283
Enrollment
Unknown
Registered
2022-02-03
Start date
2022-02-01
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Orthopaedic implant/prosthesis

Interventions

Clinical Rehabilitation Treatment Group:None

Sponsors

Zhanlanlu Hospital,Xicheng District,Beijing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.The first diagnosis was lower limb fracture (femur,tibia,,fibula,ankle,foot bone) and soft tissue(ligament, meniscus, etc.)fracture, the lower femur or patella fracture; 2.Aged >= 18 years; 3.Willing to participate and cooperate in completing the study; 4.Fracture reduction, internal fixation stability and soft tissue repair was in good condition; 5.Other diseases that do not require special treatment during hospitalization and do not affect the implementation of the clinical pathway for the first diagnosis can enter the study

Exclusion criteria

Exclusion criteria: 1.Upper limb or lower limb trauma, infection, tumor, congenital malformation and other diseases affecting upper limb or lower limb function; 2.Patients with serious postoperative complications during hospitalization that affected the study results; 3.Patients who took drugs within one month before enrollment or for a long time that might affect the study results, such as hormones and analgesics; 4.Intolerant to morphine or other analgesic and sedative drugs; 5.Moderate or severe anxiety or depression (SDS/SAS score > 61 or clinically diagnosed anxiety disorder, depression or bidirectional disorder and other abnormal psychological disorders); 6.The patient has consciousness or cognitive impairment or severe mental illness, and cannot cooperate with rehabilitation treatment; 7.Unwilling to participate in this research.

Design outcomes

Primary

MeasureTime frame
The intensity of pain;Emotion;

Secondary

MeasureTime frame
Basic morphology assessment;Basic motor function assessment;Special function assessment;Cognitive function;Activity of dailiy life assessment;Quality of life assessment;Biochemical index;

Countries

China

Contacts

Public ContactJingxinmiao Lin

Zhanlanlu Hospital,Xicheng District,Beijing

ljxm_aurora19@163.com+86 153 1363 6755

Outcome results

None listed

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