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CompletedNCT05969366Updated Aug 1, 2023

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

An observational study in Arthroplasty Complications, sponsored by Central Hospital, Nancy, France. Completed at 1 site in France. Open to participants aged 85 Years and older. Per ClinicalTrials.gov, last updated 2023-08-01.

Sponsored by Central Hospital, Nancy, France · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
79
Ages
85 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Arthroplasty Complications
03

In context

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
85 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Any people of 85 years of more who received total hip arthroplasty with uncemented stem fully hydroxyapatitis coated

Inclusion criteria

  • receive total hip arthroplasty with uncemented stem fully hydroxyapatites coated

Exclusion criteria

Exclusion Criteria:

  • trauma context
  • less than 3 month follow up
  • Any surgery of the hip as medical history
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
79 participants (actual)
Patient registry
No

Groups and cohorts

  • patients 85 yearsold or orlder who hab total hip replacement with uncemented femoral stem

    Procedure: Total hip arthroplasty

Interventions

  • ProcedureTotal hip arthroplasty
06

What researchers measure

Primary outcomes

  1. rate of complication

    survival study, any complications

    Time frame: minimum of 3 months follow up

Secondary outcomes

  1. risk factor of complications

    Time frame: minimum of 3 months follow up

07

Study locations

1 site
  • Centre Chirurgical Emile Gallé
    Nancy, 54000, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05969366
Lead sponsor
Central Hospital, Nancy, France
Responsible party
Olivier ROCHE (Praticien Hospitalier, Central Hospital, Nancy, France) — Principal investigator
First posted
Aug 1, 2023
Start date
Jun 2015
Primary completion
Apr 2016
Completion
Jul 2023
Last update
Aug 1, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.

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