Clinical Trials Logo

Hip clinical trials

View clinical trials related to Hip.

Filter by:

NCT ID: NCT06053060 Completed - Arthropathy Clinical Trials

Evaluation of the Positioning of the Dynacup Cup "One C" Versus "Standard Dynacup"

DYNACUP
Start date: November 21, 2021
Phase: N/A
Study type: Interventional

The ceramic-ceramic friction pair is widely used today in total hip arthroplasty, including fourth-generation ceramics which show the lowest wear rate. These have considerably reduced the risk of head fracture compared to previous generations; however, the risk of insert rupture persists with rates similar to those of third generation ceramics. These ceramic fractures require complex revision surgery, which brings complications, exposing patients to the risk of third-body wear and tear related to persistent post-surgical debris. They are frequently due to an incorrect assembly of the ceramic causing intraoperative or early postoperative rupture. To fix this, manufacturers have developed pre-assembled cups in the factory. The Dynacup One C cup developed by Corin® corresponds to the pre-assembled version of the Dynacup cup, making it possible to eliminate the risk of anomaly during intraoperative assembly linked to the human factor and to offer patients with very small cups an adapted ceramic implant. A single study with a small sample compared the two implants (pre-assembled version [vs] modular version) clinically, radiologically and functionally without showing any significant difference. The lack of data in the literature comparing these two implants motivated us to conduct a randomized comparative study on a large sample of patients.

NCT ID: NCT05754905 Completed - Hip Clinical Trials

High-resolution CE-MRA of Children's Hip Joint

Start date: January 1, 2021
Phase:
Study type: Observational

The goal of this observational study is to learn about the feasibility of enhanced three-dimensional water-selective cartilage (3D-WATSc) sequence in displaying the vessels of children's hip by magnetic resonance. The main questions it aims to answer are: - Could the images of enhanced 3D-WATSc sequence show the healthy side hip joint vessels in children? - Could the images of enhanced 3D-WATSc sequence show the vascular disease of the suffering side hip joint in children? Participants with unilateral hip disease will undergo the magnetic resonance examination including enhanced 3D-WATSc sequence. The pelvic plain film and magnetic resonance images will be collected and analysed. Researchers will compare the images of of the normal side with the images of the abnormal side to see if the enhanced 3D-WATSc sequence images could show the vascular disease of the suffering side hip joint in children?

NCT ID: NCT05613439 Recruiting - Clinical trials for Patient Satisfaction

The Fast-track Centre for Hip and Knee Replacement Database

FCD
Start date: September 1, 2022
Phase:
Study type: Observational

This is a prospective study-registry on preoperative patient characteristics and postoperative complications in patients having fast-track hip and knee replacement surgery in 8 Danish dedicated arthroplasty departments from all five health regions in Denmark. The registry consists of detailed patient and physician reported preoperative characteristics and including prescribed medication and lab results. Follow-up is based on electronical medical records by dedicated nurses with physician backup and includes Clavien-Dindo and Comprehensive Complication Index scoring. All patients having day-surgery also completes a patient reported questionaire on health-care utilization and return to work by day 30. Finally, a machine-learning algorithm for identification of "high-risk" patients based on he preoperative data is included.

NCT ID: NCT05606120 Recruiting - Arthroplasty Clinical Trials

H-35 CL TRAUMA Cemented Femoral Stem

Start date: December 1, 2022
Phase:
Study type: Observational

Study design: monocentric, retrospective, observational and post-market clinical study. Purpose: To demonstrate the safety and performance of CL TRAUMA femoral stem. The eligible study population is represented by the entire population that underwent a hip replacement with CL TRAUMA femoral stem from 2017 to 2020 at Azienda Ospedaliera di Padova (IT) in accordance with the indication for use of the product.

NCT ID: NCT05338008 Completed - Hip Clinical Trials

Intrawound Administration of Vancomycin in THA

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the intra-articular and serum levels of vancomycin over the first 24 hours postoperatively after intra-articular administration of a standard dose of vancomycin in primary total hip arthroplasty.

NCT ID: NCT04516239 Completed - Arthroplasty Clinical Trials

Comparison of Metal on Metal Total Hip Arthroplasty and Metal on Metal Total Hip Resurfacing.

Start date: September 2005
Phase: Phase 4
Study type: Interventional

The goal of this double-blind prospective randomized study is to compare subjective outcome measures and gait parameters between conventional THA using large diameter femoral heads and total hip resurfacing

NCT ID: NCT04061993 Completed - Arthroplasty Clinical Trials

Effects of Early Home-based Strength and Sensory-motor Training After THA on Functional Outcome and Patient Satisfaction

Start date: January 9, 2018
Phase: N/A
Study type: Interventional

A prospective multicentre randomised clinical trial of 250 selected patients with THA, who will be randomly assigned to intervention (IG) or control group (CG). Both will have standard physiotherapy during hospitalisation, IG will additionally learn strength and sensory-motor training exercises. Follow up will be performed with physical tests, maximal voluntary isometric contractions and outcome assessment questionnaires at baseline and 1, 3 and 12 months after surgery.

NCT ID: NCT03850665 Completed - Osteoarthritis Clinical Trials

Comparison of Functional Outcome in Patients After Hip Arthroplasty Depending on Surgical Approach

Start date: September 27, 2020
Phase: N/A
Study type: Interventional

The aim of the study will be to compare functional outcomes of the two surgical hip approaches in total hip arthroplasty: anterior, posterolateral and anterolateral. Surgical approach may have influence on patients functional outcome.

NCT ID: NCT02829866 Completed - Arthroplasty Clinical Trials

AMIStem-H Radiographic Analysis

Start date: September 2010
Phase:
Study type: Observational

Total hip replacement (THP) is widely used for hip osteoarthritis treatment. Surgeons are constantly looking to improve all aspects related to this procedure weather is improvement of implant design, instrumentation or surgical technique. Excellent clinical and radiological results were observed at medium and long term in the last years for AMIStem system. This observational study has the objective to survey hip prosthesis stability and function of the operated hip in patients who are not exposed to surgical risks. The principal investigator will contact all patients in order to perform the follow-up visit according to standard practice. Patients operated between January 2010 and December 2011 will be invited in the study during the clinical visit organised according to standard practice. Preoperative clinical and radiological data, intraoperative details and postoperative follow-up data at 1-year will be retrospectively collected. Five-year and ten-year data will be prospectively collected after inclusion in the study.

NCT ID: NCT00906295 Completed - Anemia Clinical Trials

Establishment of Optimal Transfusion Threshold After Major Orthopedic Surgery

Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a higher threshold for transfusion with red blood cells improves the postoperative ambulation.