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Total Hip Replacement clinical trials

View clinical trials related to Total Hip Replacement.

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NCT ID: NCT06409312 Not yet recruiting - Clinical trials for Total Hip Replacement

Digital Healthcare App After Total Hip Arthroplasty

Start date: May 21, 2024
Phase: N/A
Study type: Interventional

This study examines the effectiveness of rehabilitation after hip replacement surgery using a specialised app called Akina Cloud. Medical professionals at the Schulthess Clinic will provide detailed information about the study. Participants must meet certain eligibility requirements. There will be time for consideration before enrolment. A demonstration of how to use the app will be provided upon agreement. Participants will be shown how to set up their profile and interact with a real therapist who will provide feedback. The initial 30-minute introduction is scheduled to take place a few days after surgery while still in hospital. Participants will be asked to complete several questionnaires. The rehabilitation process involves using the app for at least 12 weeks, at least three times a week, for 20-30 minutes per session. Direct communication with the therapist via the app is available for any queries. Follow-up questionnaires will be emailed at 6 and 12 weeks, after training, and again at 26 weeks to assess progress and feedback on the use of the app. Each session with the app lasts about 20 minutes and the questionnaire takes about 30 minutes to complete.

NCT ID: NCT06238960 Recruiting - Telerehabilitation Clinical Trials

Effectiveness of Telerehabilitation in Continuity With Outpatient Physiotherapy After Total Hip Replacement.

Start date: February 10, 2024
Phase: N/A
Study type: Interventional

Total arthroplasty (THA) is the treatment of choice for severe osteoarthritis of the hip joint. Following this type of intervention, a multidisciplinary rehabilitation approach allows you to reduce pain and improve the ability to carry out activities of daily living (ADL), but it is not clear what the optimal rehabilitation program is. Recently, the use of telerehabilitation has increased over the years. Specifically, in treatment of patients following THA surgery, telerehabilitation is able to give similar results to the treatment performed in person terms of pain and function. The aim of this study is to verify whether telerehabilitation associated with In-person treatment is comparable in terms of pain, recovery functionality and patient participation and satisfaction, compared to those provided by rehabilitation alone in the presence of patients undergoing THA surgery.

NCT ID: NCT06209216 Recruiting - Clinical trials for Total Hip Replacement

Twenty-Four Seven Functional Status in Total Hip Replacement

LEARNT
Start date: December 13, 2023
Phase:
Study type: Observational

The goal of this observational study is to define digital remote monitoring measures for functional status (activities of daily living) in patients receiving total hip replacement. Functional status will be collected using a study iPhone and two wearable wrist monitors.

NCT ID: NCT06169878 Completed - Clinical trials for Total Hip Replacement

Efficiency of the Adjustable Lower Extremity Abduction Apparatus After Total Hip Replacement Surgery

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

This study was conducted to evaluate the effect of the adjustable lower extremity abduction apparatus developed after total hip arthroplasty (TKP) surgeries on preventing dislocation and walking.The study is of randomized controlled type. It was held on the inpatient floor of a Training and Research Hospital in Istanbul, between November 2021 and October 16, 2023, with patients undergoing femoral neck fracture surgery. All patients who were admitted to this clinic for surgical intervention constituted the population of the study. In the research, 30 patients between the ages of 50-80 were included in the experimental group in which the "Adjustable lower extremity abduction apparatus" developed within the scope of the thesis was used, and 30 patients in which this apparatus was not used were included in the control group. As data collection tools in the study, "Patient Introduction Form", "Standardized Mini Mental State Test", "Patient Mobility Scale", "Modified Barthel Activities of Daily Living Index", "Apparatus Quality and Comfort Assessment Form" " and "Harris Hip Score Form" were used. Data were evaluated using IBM SPPS 27.0 statistical package program.

NCT ID: NCT06077825 Completed - Clinical trials for Total Hip Replacement

Effects of Lower Limbs Symmetrical Loading on Risk of Fall

Start date: July 15, 2015
Phase: N/A
Study type: Interventional

Objective: To assess the impact of total hip arthroplasty (THA) on functional outcomes and fall risk in patients with hip osteoarthritis. The objective was to investigate the effectiveness of physical therapy in postoperative rehabilitation and identify fall risk factors to guide fall prevention strategies after THA. Methods: A non-randomized, interventional clinical trial was conducted with 30 patients scheduled for THA. Functional outcomes were evaluated using the Harris Hip Score (HHS), 40-meter fast-paced walk test (40mFPWT), 30-Second Chair Test, and Western Ontario McMaster Universities Osteoarthritis Index (WOMAC). Balance and fall risk were assessed using the Single-Leg Standing Test and a posturography device (TETRAX). The Nottingham Health Profile (NHP) was used to measure subjective health status and quality of life. Assessments were performed preoperatively, at 6 weeks postoperatively, and at 3 months postoperatively.

NCT ID: NCT06006572 Enrolling by invitation - Clinical trials for Total Hip Replacement

Hip DAA Closure Techniques

Start date: March 1, 2023
Phase: N/A
Study type: Interventional

This study aims to analyze the difference in rates of wound complications using two different closure techniques in Direct anterior approach for primary total hip replacement.

NCT ID: NCT05429567 Completed - Clinical trials for Total Hip Replacement

Effectiveness of Patient-Controlled Intravenous Analgesia (PCIA) With Fentanyl

Start date: March 1, 2021
Phase: Phase 1
Study type: Interventional

To enhance post-operative pain management, patient-controlled intravenous analgesia (PCIA) has been employed. The fentanyl background PCIA therapy was created to solve the limitations of IV-based PCIA, such as programming errors, mobility limitations, and the risk of needle stick injuries. The goal of this trial was to observe how fentanyl patient-controlled intravenous analgesia pump (PCIA) and background infusion is worked in patients with post-total hip replacement analgesia.

NCT ID: NCT05375565 Completed - Clinical trials for Total Hip Replacement

Comparative Effects of Weight Bearing and Non-weight Bearing Exercises in Patients With Total Hip Replacement

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

to compare the effects of weight bearing and non-weight bearing exercises on pain, range of motion and disability in patients with total hip replacement

NCT ID: NCT05291598 Completed - Clinical trials for Total Knee Replacement

Meloxicam for Pain Management After Total Joint Arthroplasty (TJA)

Start date: May 1, 2022
Phase: Phase 3
Study type: Interventional

The purpose of this project is to determine if a change in patient reported pain, nausea and vomiting after total knee and hip arthroplasty could be observed with the substitution of Intravenous meloxicam for ketorolac in the current established peri-operative pain protocol and if these changes lead to a decrease in opioid consumption (in morphine equivalents).

NCT ID: NCT04903860 Completed - Clinical trials for Total Hip Replacement

Comparison of the Use of Conventional Ancillary Reaming and Single-use Ancillary Reaming Material in Total Hip Replacement

LUUC
Start date: July 12, 2021
Phase: N/A
Study type: Interventional

The main objective of the study is to compare the use of single-use ancillary reaming material during total hip replacement and conventional reusable ancillary reaming material. The assessment will focus on the medico-economic differences found in this prospective randomized study