Clinical trials: Acetabular Surgery
Acetabular Fracture
Treatment of Acetabular Fractures in Elderly Patients
This retrospective study investigates surgical treatment of acetabular fractures in elderly patients (>60 years of age), either undergoing joint-preserving surgery or joint- replacement.
- Trial name
- ACETA (NCT03929536)
- Where
- Switzerland
- Volunteers
- 211 people
- Sponsor
- University Hospital, Basel, Switzerland
Acetabular Fractures, Both Columns
Acetabular Fractures of Both Columns
The purpose of this research is to study a specific acetabular (hip socket) fracture pattern and how its treatment affects the functional, clinical, and x-ray outcomes. There are no experimental procedures involved.
- Trial name
- NCT00676611
- Where
- United States
- Volunteers
- 52 people
- Sponsor
- Milton S. Hershey Medical Center
Femoro Acetabular Impingement
Weightbearing Restrictions on Postoperative Outcomes Following Arthroscopic Surgery for FAI
The purpose of this single-blinded (assessor) randomized trial is to compare patient-reported, clinical and functional outcomes in patients randomized to weight-bearing as tolerated (WBAT) or partial weight-bearing (PWB)…
- Trial name
- NCT05280899
- Testing
- Weight-bearing As Tolerated, Partial Weight-bearing
- Where
- Canada
- Volunteers
- 88 people
- Sponsor
- Panam Clinic
Acetabular Fractures, Hip Replacement
Multicenter Retrospective Evaluation of the Surgical Management of Spinal Growth Dystrophy
Spinal growth dystrophy (CRD), also called Scheuermann's disease, corresponding to impaired vertebral structure occurring in children and adolescents with involvement of the growth cartilage causing impaired growth and kyphosis.
- Trial name
- DRC (NCT02904681)
- Testing
- No intervention. Observational and descriptive study
- Where
- France
- Volunteers
- 16 people
- Sponsor
- Fondation Hôpital Saint-Joseph
Hip Replacement, Primary, Secondary or Post-traumatic Osteoarthrosis
Observational Study to Evaluate Long-Term Outcome in Hip Arthroplasty
This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.
- Conditions
- Hip Replacement, Primary, Secondary or Post-traumatic Osteoarthrosis, Femur Head Necrosis, Congenital Dislocations
- Trial name
- NCT02230826
- Where
- 13 sites in France
- Volunteers
- 2,500 people
- Sponsor
- Corin