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Recruiting NCT07597538

Change of Knee Phenotype After Total Hip Arthroplasty

Observational Knee Phenotype Changes After THA Coronal Plane Alignment of the Knee

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Knee Phenotype Changes After THA, Coronal Plane Alignment of the Knee. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluation of Knee Phenotype Following Total Hip Arthroplasty :A Prospective Cohort Study

Overview

this study evaluates changes in knee phenotype after total hip arthroplasty using radiographic assessment of coronal alignment in a prospective cohort of patients

Detailed description

this prospective cohort study evaluates the effect of total hip arthroplasty on knee phenotype using pre and post operative full-length radiographic assessment coronal alignment parameters will be measured to assess changes in knee biomechanics following THA

Primary outcome measures

  • knee phenotype change following total hip arthroplasty [Time frame: Immediately postoperatively"]

Eligibility criteria

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Department of orthopedic surgery faculty of medicine assiut university — Asyut

Identifiers

NCT: NCT07597538 · THA-Knee-phenotype-2026

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗