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Total Hip Replacement clinical trials

View clinical trials related to Total Hip Replacement.

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NCT ID: NCT03424382 Completed - Stroke Clinical Trials

CREATION Health Readmission Risk Assessment Tool

Start date: May 15, 2017
Phase:
Study type: Observational

This study occurs in two phases. Phase 1 involves initial item development and measurement validation of a new tool for identifying hospitalized patients at high risk for preventable readmission. Primary tasks include item construction and content validation, data collection, analysis, and instrument refinement. Phase 2 involves administering the refined instrument to a new group of patients to determine final item content for the instrument, its factor structure, and its predictive validity.

NCT ID: NCT03218267 Completed - Clinical trials for Total Hip Replacement

The Postural Control in Patients After Total Hip Replacement

Start date: September 1, 2014
Phase: N/A
Study type: Interventional

Total hip replacement (THR) is the procedure which can improve the quality of life in patients with osteoarthritis. However, deficits in static stability and impairment of the lower limb efficiency can be observed even several months after procedure. The aim of this study was to investigate the static balance of the standing position in patients treated by THR.

NCT ID: NCT03189290 Completed - Postoperative Pain Clinical Trials

Study of the QUadratus Lumborum Bloc in Total Hip ARthroplasty: Efficacy and Safety

SQUARE
Start date: July 6, 2017
Phase: N/A
Study type: Interventional

The purpose of this prospective research study is to determine the best way to manage post-operative pain after a total hip arthroplasty. Currently, there is no standard of care for managing post-operative pain in these patients. The quadratus lumborum block (QLB) first described by Blanco in 2007, is a promising technique in this indication: recently, there is a growing evidence for the use of the QLB as an alternative technique for pain management after hip surgery.

NCT ID: NCT03072706 Completed - Clinical trials for Total Hip Replacement

Evaluation of X-ray, Acetabular Guides and CT in THR

EXACT
Start date: November 7, 2017
Phase: N/A
Study type: Interventional

Total hip replacement is one of the most successful surgical procedures of modern times, with over 80,000 performed each year in the UK. However, up to 5% of all primary hip replacements need to be revised within the first 10 years, and in many cases malposition of the acetabular (hip socket) component is implicated in the early failure. The standard method of positioning the acetabular component is for the surgeon to be guided by a combination of the visible anatomical landmarks within the surgical field, and the wider environment of the operating theatre. The advent of 3D printing has led to the development of custom-made surgical guides which can be used during surgery, in order to assist the surgeon in the positioning of instruments and devices. These surgical guides are manufactured based on CT or MRI imaging, and are designed to clearly indicate to the surgeon the desired location and orientation of bony cuts and implant positions. This study will test the hypothesis that an acetabular alignment guide combined with three-dimensional CT-based planning using the Corin OPS™ (Optimised Positioning System), provides more accurate component alignment following primary total hip replacement compared with the current standard treatment, with the aim of improving patient outcomes and reducing the risk of complications of total hip replacement.

NCT ID: NCT03064165 Completed - Clinical trials for Total Hip Replacement

Postoperative Analgesia After Elective Hip Surgery - Effect of Obturator Nerve Blockade

Start date: August 15, 2017
Phase: Phase 4
Study type: Interventional

The study investigates the effect of an obturator nerve block on the postoperative pain and opioid consumption after total hip replacement.

NCT ID: NCT02861638 Completed - Clinical trials for Total Hip Replacement

Action Observation in Hip Replacement

Start date: April 2014
Phase: N/A
Study type: Interventional

Postoperative rehabilitation is required for a successful outcome following total hip arthroplasty. Traditionally rehabilitative programs aim to increase range of motion, to strengthen quadriceps, to restore normal gait, and to recover independence in activities of daily living. In the last decade action observation treatment, in addition to conventional physiotherapy has been proposed as a treatment method in rehabilitative medicine. There is growing evidence of the applicability of action observation training in rehabilitative medicine, indeed it has been applied in the rehabilitation of stroke of Parkinson disease of cerebral palsy and of aphasia. Nevertheless those are small studies and one of them included a mixed population of hip and knee arthroplasty.

NCT ID: NCT02720471 Completed - Clinical trials for Total Hip Replacement

Local Analgesia Versus Local Peroperative Infiltration After Total Hip Replacement

ALRIAL
Start date: September 14, 2015
Phase: Phase 3
Study type: Interventional

Clinical study, comparative, prospective, interventional, randomized, single-center, single-blind The fast resumption of the walking after surgery of total prosthesis of hip (PTH) requires an effective analgesia from the immediate post-operative period. In France, whatever is the peroperative anesthesia, the analgesic reference technique is a locoregional anesthesia (ALR) ultrasound guidance by blocks of the femoral and cutaneous nerves side of the thigh. In the Anglo-Saxon countries, in particular in Australia and in the United States, the techniques of peroperative infiltration of local anesthetics (IAL) by the surgeon supplanted the techniques of traditional ALR. However, no French study compares the IAL with the conventional ALR with a rigorous methodology. Our occasional practice of IAL suggests us that it is more effective in terms of post-operative analgesia with Analog Visual Scales decreased (EVA) and a lesser consumption of morphine. Furthermore, the resumption of the upright posture in bipedal support as well as the resumption of the walking would be earlier. The main objective is to show that the post-operative analgesia by local peroperative infiltration is superior to that obtained by locoregional anesthesia (ALR by femoral block associated with a side cutaneous block of the thigh) after the surgery of total prosthesis of hip, with decrease of the consumption of morphine within first 72 post-operative hours. The secondary objectives are to compare the Analog Visual Scales of pain (EVA) with the rest and with the mobilization during various times (in post-surgery care room, then at H4, H8, H12, H24, H48, H72), the period between the end of intervention (out of the operating room) and the first support by the upright posture in bipedal support), the period between the end of intervention and the resumption of the walk, the satisfaction of the patients at the exit of the hospital, the duration of hospitalization after the surgical operation and the possible unwanted events (systematic toxicity of the local anesthetics, the infection of prosthesis, disease thromboembolic venous) during the hospitalization.

NCT ID: NCT02644096 Completed - Rehabilitation Clinical Trials

Rehabilitation of Patients After THR - Based on Patients´Selfrated Health

Rehab-THR
Start date: September 2004
Phase: Phase 1
Study type: Interventional

Objective: The investigators hypothesized that all areas of health status after total hip replacement could be improved in patients aged over 65 years and over by using telephone support and counselling 2 and 10 weeks after surgery compared with a control group receiving conventional care and treatment. Design: A randomised clinical trial focusing on patients' health status by using SF-36 at 4 weeks pre- and 3 and 9 months postoperatively was carried out. Sample: 180 patients aged 65 and over were randomised 4 weeks preoperatively to either control or intervention groups. Measurements: Both groups received conventional surgical treatment, but the intervention group was interviewed by telephone 2 and 10 weeks after surgery. Patients were given counselling within eight main dimensions with reference to their postoperative situation. Key-words: THR - elderly patients - health status - postoperative support - counselling

NCT ID: NCT02554149 Completed - Arthroplasty Clinical Trials

Radiological Measurement of Femoral Stem Version Using Lateral Decubitus Method: A Prospective Study

Start date: September 2015
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study was to develop a radiological method to measure stem anteversion and to determine its validity and reliability.

NCT ID: NCT02536573 Completed - Clinical trials for Total Hip Replacement

Study of Total Hip Arthroplasty Using Radlink Surgical Positioning Software

Start date: December 2015
Phase: N/A
Study type: Interventional

This is a prospective, randomized study of total hip arthroplasty with and without the use of Radlink surgical positioning software. The investigators are interested in discovering whether the use of the Radlink software will provide more accurate acetabular cup position when compared with surgeon estimates based on visual inspection of fluoroscopic images.