Change of Knee Phenotype After Total Hip Arthroplasty
THA-KP
Evaluation of Knee Phenotype Following Total Hip Arthroplasty :A Prospective Cohort Study
1 other identifier
observational
500
1 country
1
Brief Summary
this study evaluates changes in knee phenotype after total hip arthroplasty using radiographic assessment of coronal alignment in a prospective cohort of patients
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2026
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 10, 2026
CompletedFirst Posted
Study publicly available on registry
May 19, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2028
May 19, 2026
May 1, 2026
2 years
April 10, 2026
May 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
knee phenotype change following total hip arthroplasty
knee phenotype change will be assessed using full-length radiographs by comparing coronal alignment parameters before and after total hip arthroplasty
Immediately postoperatively"
Eligibility Criteria
the study population will include any patient undergoing primary unilateral total hip arthroplasty for hip joint pathology .patient will be recruited consecutively from the orthopedic surgery department . all eligible patients will be assessed preoperatively and followed postoperatively with full length lower limb radiographs to evaluate changes in knee phenotype and coronal alignment
You may qualify if:
- patients scheduled for primary unilateral total hip arthroplasty
- patient with hip joint pathology indicated for THA ( osteoarthritis )
- ability to provide informed consent
- availability for pre and post- operative radiographic follow-up
You may not qualify if:
- refusal to participate or withdraw consent
- incomplete radiographic data or loss to follow up
- previous surgery on the ipsilateral hip or knee
- patients with neuromuscular disorders affecting alignment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of orthopedic surgery faculty of medicine assiut university
Asyut, Asyut Governorate, 71515, Egypt
Study Officials
- PRINCIPAL INVESTIGATOR
mohamed kamal abdelnasser, MD professor orthopedic
faculty of medicine assiut univerisity
- PRINCIPAL INVESTIGATOR
mohamed anter ali, MD Doctor orthopedic surgery
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- resident orthopedic surgery
Study Record Dates
First Submitted
April 10, 2026
First Posted
May 19, 2026
Study Start
February 1, 2026
Primary Completion (Estimated)
February 1, 2028
Study Completion (Estimated)
August 1, 2028
Last Updated
May 19, 2026
Record last verified: 2026-05