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NCT05969366 Clinical Trial

Early Clinical and Radiological Outcomes of Uncemented Fully Coated Stem With Patients of 85 Years and More, Complications and Risks Factor

Arthroplasty Complications Clinical Trial

Official title:
Early Clinical and Radiological Outcomes of Uncemented Fully Coated Stem With Patients of 85 Years and More, Complications and Risks Factor

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05969366
Other study ID # 2022PI032
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2015
Est. completion date July 2023

Study information
Verified date July 2023
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective, single-centre study. Review of patients aged 85 and over who underwent total hip replacement between June 2015 and February 2022. This is a femoral stem survival study with calculation of the complication rate in this population. The study does not focus on total hip replacements in the context of trauma. The secondary endpoint was the search for complication risk factors.

Recruitment information / eligibility
Status Completed
Enrollment 79
Est. completion date July 2023
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender All
Age group 85 Years and older
Eligibility Inclusion Criteria: - receive total hip arthroplasty with uncemented stem fully hydroxyapatites coated Exclusion Criteria: - trauma context - less than 3 month follow up - Any surgery of the hip as medical history

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Total hip arthroplasty

Locations
Country Name City State
France Centre Chirurgical Emile Gallé Nancy

Sponsors (1)
Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary rate of complication survival study, any complications minimum of 3 months follow up
Secondary risk factor of complications minimum of 3 months follow up
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