Clinical Trials Logo

Hip Arthroplasty clinical trials

View clinical trials related to Hip Arthroplasty.

Filter by:

NCT ID: NCT06009432 Not yet recruiting - Hip Arthroplasty Clinical Trials

Efficacy of Proprioceptive Neuromuscular Facilitation Exercise Program in Total Hip Arthroplasty

Start date: September 1, 2024
Phase: N/A
Study type: Interventional

This study was planned to investigate the effectiveness of usual care and additional proprioceptive neuromuscular facilitation exercise program in patients undergoing total hip arthroplasty surgery. It is aimed to evaluate pain intensity, disability level, proprioception, kinesiophobia, balance and functional status of the patients. The study will be conducted with volunteer patients who are followed up by the Orthopedics and Traumatology outpatient clinic of Fethiye State Hospital and who have undergone total hip arthroplasty surgery. The evaluations will be performed in the Orthopedics and Traumatology outpatient clinic of Fethiye State Hospital. It is aimed to evaluate at least 42 patients for the study. The first evaluation will be performed 6 weeks post-operatively and the second evaluation will be performed 2 months after treatment.

NCT ID: NCT06009419 Not yet recruiting - Hip Arthroplasty Clinical Trials

Effectiveness of Dual Task Training in Total Hip Arthroplasty

Start date: December 1, 2024
Phase: N/A
Study type: Interventional

This study was planned to investigate the effectiveness of usual care and dual task program in patients who underwent total hip arthroplasty surgery. It is aimed to evaluate pain intensity, disability level, mini mental status, coordination, balance and functional status of the patients. The study will be conducted with volunteer patients who are followed up by the Orthopedics and Traumatology outpatient clinic of Muğla Training and Research Hospital and who have undergone total hip arthroplasty surgery. The evaluations will be performed in the Orthopedics and Traumatology outpatient clinic of Muğla Training and Research Hospital. It is aimed to evaluate at least 24 patients for the study.

NCT ID: NCT05807828 Recruiting - Osteoarthritis, Hip Clinical Trials

VR Simulation and Basic Skills in THA

MD-VR-THA
Start date: March 26, 2023
Phase: N/A
Study type: Interventional

This prospective randomised clinical trial aims to test if virtual reality (VR) simulation helps acquire basic surgical skills in total hip arthroplasty (THA) by medical students. The main question[s] it aims to answer are: 1. Can VR simulation develop the medical students' basic surgical skills and medical knowledge in THA? 2. Will VR simulation become a part of orthopaedic surgical education? Participants will be randomised into two groups (VR and control). 1. They will be asked to watch a very detailed video explaining basic rules and skills in implanting the acetabular cup and femoral stem in THA 2. The VR group will perform at least three VR THA sessions concerning cup (inclination) and stem (version) implantation 3. Then all participants will be asked to implant a cup and a stem in a predefined inclination and version, respectively, in sawbones 4. The mean difference between the predefined and the actual implanted cup inclination and version of the stem will be compared between groups

NCT ID: NCT05197660 Completed - Surgery Clinical Trials

Routine Surgical Procedures During COVID-19 Pandemic: a French Nationwide Cohort Study

Start date: January 1, 2019
Phase:
Study type: Observational

Determine the consequences of COVID-19 pandemic on routine targeted surgeries. Five surgical procedures were considered : cataract surgery, hip and knee arthoplasties, coronary revascularisation by angioplasty and definitive cardiac stimulation. The objective of the study is to quantify changes of these procedures in 2020 and in 2021 (up to June) compared to 2019 taking into account their annual evolution and according to the type of operation (primary or reoperation/revision) and emergency status, if applicable.

NCT ID: NCT04791605 Completed - Hip Fractures Clinical Trials

Gait Pattern Between a Cemented and Non-cemented Femur Stem

Start date: January 1, 2012
Phase: N/A
Study type: Interventional

Acute cervical femoral neck fracture patients randomized to either cemented or non-cemented stem. The investigators used gait analysis to evaluate if patients operated with a cemented stem showed more favourable hip kinematics and kinetics when compared with a group of patients operated with a non-cemented stem.

NCT ID: NCT04592939 Enrolling by invitation - Postoperative Pain Clinical Trials

Trial of Weight Bearing Status Following Femoral Revision With Tapered, Fluted, Titanium Stems

Start date: October 19, 2020
Phase: N/A
Study type: Interventional

This is a prospective, randomized controlled trial of all patients undergoing femoral revision at Thomas Jefferson University Hospital and Rothman Institute undergoing femoral revision surgery with the use of a modern titanium, fluted, tapered stem. At the time of surgery, patients will be randomized to six weeks of toe-touch weight bearing or immediate weight bearing as tolerated

NCT ID: NCT04506450 Completed - Hip Arthroplasty Clinical Trials

Peripheral Nerve Block vs Spinal Anesthesia in Hip Surgery

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Anesthesia plays an important role in the patient's outcome: each anesthesiological technique has a different cardiovascular impact, because they act differently on the autonomic nervous system, which in turn regulates heart rate, myocardial contractility and vascular tone. Subarachnoid anesthesia can result in a reduction in cardiac output, hypotension and bradycardia due to blockage of the nerve fibers of the sympathetic system, while peripheral nerve block is associated with a lower impact on the autonomic nervous system, therefore less influence on hemodynamic changes compared to subarachnoid anesthesia. Hypotension can lead to myocardial ischaemia, especially in patients at high surgical risk. In addition, peripheral nerve block allows for better coverage from postoperative pain compared to subarachnoid anesthesia in patients undergoing hip surgery. This leads to less postoperative stress, with less impact on cardiac and respiratory function. Numerous studies have shown the efficacy and safety of regional anesthesia in hip surgery. This study aims to compare the hemodynamic changes of subarachnoid anesthesia and peripheral nerve block in patients who underwent total and partial hip replacement

NCT ID: NCT04426058 Recruiting - Pain, Postoperative Clinical Trials

CMP vs Fascia Iliaca Block

Start date: June 6, 2020
Phase: N/A
Study type: Interventional

Complete motorsparing protocol (CMP) has been developed to try to minimize the motor nerve block that is created when using Facia iliaca nerve block. The blocks performed in the (CMP) are the cluneal nerve block, Pericapsular nerve group block and lateral femoral cutaneous block. On the clinical trial, the investigators will randomize the participants that meet criteria to CMP or Fascia iliaca Block and compare the amount of opioid needed post op during 24 hours and their pain scores.

NCT ID: NCT04304287 Completed - Hip Arthroplasty Clinical Trials

The Benefit of Autologous Blood Transfusion in Total Hip Arthroplasty

Start date: January 16, 2011
Phase: N/A
Study type: Interventional

The investigators studied the benefit of preoperative autologous blood donation in participants who undergo total hip arthroplasty. Study is made as a prospective and randomized.

NCT ID: NCT04301687 Not yet recruiting - Hip Arthroplasty Clinical Trials

FAB Block vs. Placebo for Hip Arthroplasty Patients

Start date: December 2024
Phase: N/A
Study type: Interventional

Hip arthroplasty surgery can be associated with significant pain. A regional anesthesia technique, the femoral articular branch block (FAB), has recently been proposed to collectively block terminal femoral and accessory obturator nerve branches to the hip joint with a single injection, theoretically blocking most of the innervation relevant to hip arthroscopy while sparing the main femoral nerve branches to the quadriceps muscles. The investigators aim to demonstrate the analgesic benefits of FAB. The investigators hypothesize that FAB will reduce opioid consumption and improve postoperative quality of recovery in patients having hip arthroplasty. This is a randomized, controlled, double-blind study and half the patients will be randomized to receive the femoral articular branch block and the other half of patients will be randomized to receive a placebo block. A comparison of pain will be made between both groups.