Skip to main content
Clinical Trials/NCT04333316
NCT04333316
Completed
Not Applicable

Principal Investigator

Tanta University0 sites180 target enrollmentJanuary 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patient Satisfaction
Sponsor
Tanta University
Enrollment
180
Primary Endpoint
clinical evaluation
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Although the success of total hip arthroplasty, many patients were dissatisfied postoperatively. Patient's reported outcome measures become of a great importance in assessment of the results after joint replacement. The aim of this prospective study is to evaluate and compare postoperative patient's satisfaction after implantation of two commonly used different designs of total hip arthroplasty.

Detailed Description

The investigators conducted a prospective comparative study carried out on 180 patients suffering of hip arthritis between 2011 and 2018. They were randomized into two groups of homogenous demographic and clinical data. Group A was treated by cementless T.H.A. with a large head while group B received cementless T.H.A. with a dual mobility cup. Clinical evaluation and preoperative patient's expectation were assessed and compared to the postoperative satisfaction.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
August 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

ahmed m. samy

assistant professor

Tanta University

Eligibility Criteria

Inclusion Criteria

  • Unilateral hip arthritis
  • Age up to 65 years
  • Body mass index (BMI) up to 35
  • Modified Charnley comorbidity classification equal to A

Exclusion Criteria

  • Neurological deficit (e.g. Parkinsonism, stroke)
  • Bone type c not fit for cementless fixation
  • Poly-arthritis, active inflammatory arthritis (e.g. rheumatoid arthritis)
  • Any patient with psychiatric disorders

Outcomes

Primary Outcomes

clinical evaluation

Time Frame: about 5 years

WOMAC score

patient's satisfaction

Time Frame: about 5 years

measurement by patient's reported outcomes measures

pain assessment

Time Frame: about 5 years

VAS score

Similar Trials