CClinicalTrials.gg
CompletedNCT05029648ERATOUpdated Jul 3, 2024

Evaluation of Predictive Factors for Psoas Tendinitis After First-line Total Hip Arthroplasty

An observational study in Psoas Tendinitis, sponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-07-03.

Sponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
1,199
Ages
18 Years and older
Sex
All
01

Study summary

Evaluation of predictive factors for psoas tendinitis after first-line total hip arthroplasty.

A single-centre retrospective study of medical data from the medical records of patients undergoing total hip arthroplasty.

Read the detailed description

From the medical records of a series of patients operated on for total hip arthroplasty:

Main objective: To assess individual and surgical factors associated with the development of psoas tendinitis.

Secondary objectives:

  • To describe the frequency of occurrence of psoas tendinitis
  • To describe the outcome of patients who underwent tenotomy.
02

Conditions studied

  • Psoas Tendinitis

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03

In context

Tendinopathy

413 studies on the registry are indexed under Tendinopathy; 64 are open to participants now.

This study's enrollment of 1,199 is above the median of 67 across 52 observational studies indexed under Tendinopathy.

Browse Tendinopathy studies →

Lead sponsor

GCS Ramsay Santé pour l'Enseignement et la Recherche is the lead sponsor of 198 studies on the registry; 94 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Patients who have had a total hip replacement for at least six months.

Inclusion criteria

  • Patient aged 18 years or older, having been informed of the research
  • Patient who has had a total hip replacement implanted for at least six months as a first-line treatment
  • Patient who has been regularly monitored since the operation and for whom all clinical and radiological data are available during follow-up visits

Exclusion criteria

Exclusion Criteria:

  • Patient undergoing revision surgery
  • Patient who has indicated his opposition to the use of his medical data
  • Patient under legal protection, guardianship or curators
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
1,199 participants (actual)
Patient registry
No

Groups and cohorts

  • Cohort

    Simple cohort

    Other: Cohort

Interventions

  • OtherCohort

    Cohort

06

What researchers measure

Primary outcomes

  1. Psoas tendinitis development

    Pain remission after tenotomy.

    Time frame: 6 months

Secondary outcomes

  1. Psoas tendinitis occurrence frequency

    Frequency of occurrence of psoas tendinitis

    Time frame: 6 months

  2. To describe the outcome of patients who have undergone tenotomy

    To describe the outcome of patients who have undergone tenotomy

    Time frame: 6 months

07

Study locations

1 site
  • Clinique de la Sauvegarde
    Lyon, 69009, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05029648
Lead sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Responsible party
Sponsor
First posted
Aug 31, 2021
Start date
Aug 11, 2011
Primary completion
Jun 19, 2024
Completion
Jun 19, 2024
Last update
Jul 3, 2024

Study contacts

Nicolas BONIN, MD
principal investigator · Clinique de la Sauvegarde

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 2024. You cannot join it, but the record below documents what was studied.

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