A standard versus without hip precaution protocol on functional recovery of hip fracture patients after hemiarthroplasty via piriformis-sparing posterior approach: A randomized controlled trial study
Phase 2
- Conditions
- This research is designed to compare the quality of life through EQVAS score between hip precaution and no hip precaution group in patient with age 60 or more who diagnosed femoral neck fracture and indicated for hemiarthroplasty via Piriformis-sparing posterior approach.hip precaution, quality of life, dislocation, piriformis sparing. no hip precaution, bipolar, hemiarthroplasty
- Registration Number
- TCTR20240523001
- Lead Sponsor
- Department Orthopaedic Surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Patient with age 60 or older diagnosed with femoral neck fracture who indicated hemiarthroplasty via Piriformis-sparing posterior approach
Exclusion Criteria
1.Neuromuscular disorder
2.Developmental dysplasia of the hip
3.Cognitive impairment by Thai Mental State Examination (TMSE) equal to or less than score of 23
4.Pathologic fracture
5.Multiple fracture
6.Previous hip fracture
7.Charlson comorbidity index score 6 or above
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method EQVAS score 0, 2, 6, 12 weeks and 1 year Counts the point
- Secondary Outcome Measures
Name Time Method umeric pain rating scale 0, 2, 6, 12 weeks and 1 year counts the point,Barthel index 0, 2, 6, 12 weeks and 1 year counts the point,Ability for basic movement scale II (ABMS II score) 0, 2, 6, 12 weeks and 1 year counts the point,Patient satisfactory outcome 0, 2, 6, 12 weeks and 1 year counts the point,Dislocation 0, 2, 6, 12 weeks and 1 year Measured as number