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RecruitingNCT06803914Updated Jul 9, 2026

Analysis of Biomechanical Parameters and Return to Sport After Total Hip Replacement

An observational study in Hip Arthroplasty, Total, sponsored by Clinique du Sport, Bordeaux Mérignac. Recruiting at 1 site in France. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-07-09.

Sponsored by Clinique du Sport, Bordeaux Mérignac · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Jan 2025; still recruiting 1 year 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This prospective study aims to evaluate the dynamic biomechanical parameters of gait in active patients who have undergone total hip replacement (THR), focusing on movements critical for return to sport.

02

Conditions studied

  • Hip Arthroplasty, Total
03

In context

Lead sponsor

Clinique du Sport, Bordeaux Mérignac is the lead sponsor of 11 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Active patients (low to high level of physical activity priori to surgery) with hip osteoarthritis necessiting total hip replacement

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient scheduled for total hip replacement surgery
  • Active patient with low to high level of physical activity prior to surgery
  • Complete medical file

Exclusion criteria

Exclusion Criteria:

  • Contralateral hip surgery
  • Neurological disorder affecting movement (e.g. Parkinson's disease, stroke)
  • Spinal pathology affecting movement or posture
  • Dementia or inability to complete questionnaires and assessments
  • Pregnant or breast-feeding patient
  • Patient under protective supervision
  • Patient not covered by a social security scheme
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No

Groups and cohorts

  • Biomechanical analysis

    Procedure: Biomechanical analysis

Interventions

  • ProcedureBiomechanical analysis

    Biomechanical assessment is performed using a set of sensors (Qualisys Sports Marker Set - functional assessment, already in use at the Clinique du Sport) as well as 3D optoelectronic cameras and force and pressure platforms. These sensors are placed at various points on both lower limbs (hip, knee, ankle) and provide data in different planes (sagittal, frontal, transverse), as well as a comparison of both sides.

06

What researchers measure

Primary outcomes

  1. Angular measurements by biomechanical sensors

    Angle measurements at hip, pelvis, knee and ankle in the three planes of space (sagittal, frontal and transverse), measured by biomechanical sensors.

    Time frame: 6 months after surgery

  2. Vertical forces measured by biomechanical sensors

    Vertical forces, push and landing, will be evaluated for each phase of the movements. Biomechanical specific sensors will be used to measure these data

    Time frame: 6 months after surgery

07

Study locations

1 of 1 sites recruiting
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 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06803914
Lead sponsor
Clinique du Sport, Bordeaux Mérignac
Responsible party
Sponsor
First posted
Jan 31, 2025
Start date
Jan 30, 2025
Primary completion
Jul 31, 2026 (estimated)
Completion
Jan 31, 2027 (estimated)
Last update
Jul 9, 2026

Study contacts

Pierre Laboudie, MD
Contact
pierre.laboudie@gmail.com
+33671270463

Oversight

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

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