Study Evaluating the Efficacy of Joint Replacement (SEVERE)

Nicolaus Copernicus University

Status: Enrolling

Conditions: Osteoarthritis, Hip; Osteoarthritis, Knee

Treatments: Procedure: Joint replacement

Study type: Observational

Funder types: Other

Identifiers

NCT04691466

WN758

Details and patient eligibility

About

Patient-related outcomes were originally designed to measure outcomes in clinical studies. They were not developed to predict outcomes, however, different studies showed close association between values achieved preoperatively and postoperative outcomes. The aim of the present trial is to identify patients with satisfactory and unsatisfactory outcomes after joint replacement and to investigate whether there are any potential predicting potential in preoperative results of the patient-related outcomes and if there exist other predicting factors for functional recovery or treatment failure after joint replacement surgery.

Enrollment: 1,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Patients with primary or secondary hip- and knee osteoarthritis undergoing joint replacement surgery.

Exclusion criteria

1. An inability to understand the Polish language,
2. Presence of neuromuscular disease and cognitive impairment,
3. Having a prosthesis in another joint of the ipsilateral or contralateral lower limb placed within 6 months before the current surgery,
4. Having rheumatoid arthritis,
5. Symptoms in several joints (hip, knee or ankle) with expected total joint arthroplasty within 1 year.

Trial design

1,000 participants in 2 patient groups

HIP_R

Description:

Patients undergoing hip replacement surgery

Treatment:

Procedure: Joint replacement

KNEE_R

Description:

Patients undergoing knee replacement surgery

Treatment:

Procedure: Joint replacement