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Total Hip Replacement clinical trials

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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: NCT04442373 Recruiting - Clinical trials for Total Hip Replacement

Impact of Surgical Injury on Haemostatic Tests in Patients Undergoing Total Hip Replacement With Subgroup Analysis of Patients With Neoplasm

I-SIGHT-THR
Start date: January 1, 2020
Phase:
Study type: Observational

Total hip replacement (THR) is associated with extensive tissue injury and considerable blood loss that can be complicated by hyperfibrinolysis with an increased need for blood transfusion. THR in patients with cancer involving the hip joint, can reduce pain and improve or maintain the function and quality of life. However, these patients have an increased likelihood of haemostatic abnormalities, such as thrombosis or extensive blood loss. Rotational thromboelastometry is a point-of-care viscoelastic assay that can provide a measure of coagulation disorders in the above settings, and this is still under review. The objective of this prospective cohort study is to quantitate the changes in clot formation dynamics following THR with a subgroup analysis of patients with cancer.

NCT ID: NCT04256291 Recruiting - Clinical trials for Total Hip Arthroplasty

Total Hip Replacement With Ceramic on Ceramic Bearing- Clinical Follow-up Study

Start date: August 1, 2018
Phase:
Study type: Observational

The pain and severe wear of hip joints caused by osteoarthritis, rheumatoid arthritis, avascular necrosis and trauma can be subjected to total hip replacement (THR). A hip implant consists of 4 components: acetabular cup, femoral stem, articular liner and femoral head. As an ideal material for THR, ceramic possesses excellent biocompatibility and stability in the human bodies. Moreover, ceramic-on-ceramic interface is highly wear-resistant, preventing generation of wear particles. With the development of latest fourth-generation ceramic Delta, larger femoral heads can be manufactured to conform to the size of native femoral heads. The rate of some of the complications after THR, such as dislocation, can be significantly reduced. The purpose of the present study is to carry out a clinical follow up for each patient who has received the ceramic-on-ceramic THR in order to understand the clinical outcome. Furthermore, the possible complications, such as dislocation and squeaking, can be determined.

NCT ID: NCT04104204 Recruiting - Postoperative Pain Clinical Trials

The Efficacy of Pain Control After Total Hip Replacement Between Ultrasound Guided Supra-inguinal Fascia Iliaca Block and Intrathecal Morphine

Start date: December 3, 2019
Phase: N/A
Study type: Interventional

Total hip replacement is one of major orthopedic surgery which result in severe postoperative pain especially at first 24 hours. Ultrasound guided regional anesthesia has become a part of multimodal analgesia.Ultrasound guided supra-inguinal fascia iliaca block is a new technique which can consistently cover femoral and lateral femoral cutaneous nerve. And with large volume (40ml), it may cover obturator nerve. This technique already proved to be useful for acute pain control in hip fracture or postoperative control in dynamic hip screw or nail insertion operation. However, it has not been compared with intrathecal morphine for total hip replacement yet.

NCT ID: NCT03240484 Recruiting - Spinal Fusion Clinical Trials

Examining Effects of Spinal Fusion on Outcomes Following Total Hip Replacement

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

The purpose of the study is to explore the long term functional status of people who have had both a spinal fusion procedure and a total hip replacement.

NCT ID: NCT03120312 Recruiting - Clinical trials for Total Hip Replacement

Short Term and Long Term Outcome for Elderly Patients Treated With Total Hip Replacement

THR
Start date: October 30, 2020
Phase:
Study type: Observational

The is a retrospective analysis to study the characteristics of elderly patients treated with total hip replacements during past 5 years.

NCT ID: NCT02853461 Recruiting - Clinical trials for Total Hip Replacement

Biofilm Investigation on Bearing Components of Explanted Hip Joint Prosthesis

Start date: June 2014
Phase: N/A
Study type: Observational

In this study the investigators sonicate the bearing components of the explanted hip prosthesis which allows highly sensitive detection of in vivo biofilms (qualitatively and quantitatively). The hip prosthesis bearing components are composed from different material. The purpose of this study is to analyse the resistance against biofilm adhesion of ceramic, metal and polyethylene prosthesis components through microbiologic analysis of sonicates.

NCT ID: NCT02793934 Recruiting - Stroke Clinical Trials

The Pilot Project Development Of MEdical Rehabilitation System in Russian Federation

Start date: September 2015
Phase:
Study type: Observational

The Programme is focused on adult patients of any gender and age more than 18 y.o., with the next conditions: 1. Acute cerebrovascular events (ACE, ischemic stroke or intracerebral hemorrhage - specialty neurology) 2. Acute myocardial infarction (AMI, specialty cardiology) 3. Patients after total hip replacement (THR, specialty orthopaedia) The program is performed in the in-patient and out-patient rehabilitation departments in 13 regions of the Russian Federation (total 244 departments).

NCT ID: NCT01866787 Recruiting - Clinical trials for Total Hip Replacement

Study on Baroreceptor Function in Relation to Orthostatic Blood Pressure Regulation After Hip Surgery

Start date: January 2013
Phase: N/A
Study type: Observational

The purpose of this observational study is to evaluate the baroreceptor function in relation to surgical inflammation and orthostatic intolerance after elective hip arthroplasty. The main hypothesis is that baroreceptor function is attenuated after surgery and related to surgical inflammation.