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Randomized comparative study of the acetabular positioning of hip prostheses performed via the conventional posterior approach and SuperPath technique

Acetabular component positioning in total hip arthroplasty performed by conventional posterior access x supracapsular access assisted by percutaneous portal (SuperPath): a prospective randomized comparative study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8ry4d4q
Enrollment
Unknown
Registered
2024-09-13
Start date
2024-09-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip osteoarthritis

Interventions

Fifty patients will be selected from the primary hip arthroplasty list at the Institute of Orthopedics and Traumatology of the Hospital das Clínicas of the Faculty of Medicine of the University of São
E04.555.110.110.110

Sponsors

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Lead Sponsor
Instituto de Ortopedia e Traumatologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients on the primary hip arthroplasty queue who have hip osteoarthritis waiting for surgery; patient able to read and understand the informed consent form.

Exclusion criteria

Exclusion criteria: Patients under 18 years of age; neurological or orthopedic diseases that alter the gait pattern and may influence functional tests; need for additional procedures in addition to hip prosthesis (shortening osteotomies, need for structured or impacted bone graft and ankylosed hips or those requiring in situ osteotomy).

Design outcomes

Primary

MeasureTime frame
Assessment of the positioning of the acetabular component of the prosthesis using pelvic tomography

Secondary

MeasureTime frame
The secondary outcomes analyzed will be: surgical time; bleeding (assessed by pre and post hemoglobin count); presence of orthopedic complications (dislocation, infection, periprosthetic fracture, neurological injury, aseptic loosening) and clinical complications (venous thromboembolism, stroke, acute myocardial infarction and death); pain in the postoperative period; and functional recovery through the "time up and go" test carried out pre-operatively, 3 days, 3 weeks, 3 months and 6 months post-operatively.

Countries

Brazil

Contacts

Public ContactLucas Oliveira

Instituto de Ortopedia e Traumatologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

lucas.torres@hc.fm.usp.br+55(11)989951629

Outcome results

None listed

Source: REBEC (via WHO ICTRP)