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Hip Arthritis clinical trials

View clinical trials related to Hip Arthritis.

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NCT ID: NCT05443243 Completed - Hip Arthritis Clinical Trials

Is a THA Stem in Varus a Risk Factor of Long-term Mechanical Complication

PTHVarus
Start date: May 13, 2022
Phase:
Study type: Observational

The objective of this study is to compare the long-term survival as well as the functional and radiographic results of the rods in the alignment of the varus to the stems in the neutral alignment by comparing 2 groups of implanted Total Hip Arthroplasty. 1 group of stems implanted in varus position. 1 group of stems implanted in neutral position

NCT ID: NCT05093361 Completed - Hip Arthritis Clinical Trials

Randomized Controlled Trial of Total Hip Arthroplasty

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of total hip arthroplasty and conservative treatment to hip pain, to activities of daily life and to the quality of life in patients with hip osteoarthritis.

NCT ID: NCT04788719 Completed - Clinical trials for Total Hip Arthroplasty

Pre and Postoperative Gait Analysis of Randomized Patient to 2 Different Cement Fixation Methods

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

The primary goal of Total Hip Replacement (THR) surgery in the treatment of hip osteoarthritis is to reduce pain and restore hip function in order to increase patient mobility and quality of life. Two different cement fixation methods are used in order to insert THR implants. This will be done before and after surgery in 2 groups randomized to either of 2 cement fixation methods. Gait analysis preoperative and 2 year after surgery.

NCT ID: NCT04775225 Completed - Clinical trials for Juvenile Idiopathic Arthritis

Hip Denervation in Juvenile Idiopathic Arthritis With Hip Arthritis

Start date: January 6, 2021
Phase: Phase 3
Study type: Interventional

Patients having juvenile idiopathic arthritis (according to ILAR criteria) with hip arthritis were divided into 3 groups. Group 1 received hip denervation and group 2 controlled and received a subcutaneous injection of saline, and group 3 received intra-articular triamcinolone. Outcome measures included pain, tenderness, range of motion, SOLAR, HARISS score. These outcomes were measured at baseline, 2 weeks, and 16 weeks

NCT ID: NCT04521842 Completed - Osteoarthritis, Hip Clinical Trials

Influence of Femoral Head Size During Total Hip Arthroplasty on Gait

Start date: January 2016
Phase: N/A
Study type: Interventional

Total hip replacement (THR) is being considered as one of the most effective medical procedures. Since its introduction, there was a worldwide debate over proper implant selection in terms of size, bearing type and shape. The diameter of used femoral heads components grew throughout the years - from 22 mm in the 1960s to 32 mm in the 2000s, which is the most commonly used size nowadays. In recent years there was a visible use of large femoral heads (>=36mm) in several registers. In the USA there was a significant grow in use of this heads rising from 1% in early 200s to even 58% in 2009. There is a strong evidence data and many researchers concerning range of movement, risk of dislocation, functional results, pain and prosthesis wear depending of femoral head size. In terms of gait characteristics there are several deviations reported concerning both patients with hip osteoarthritis (OA) and following THR. There is a lack of literature concerning influence of used implants on gait parameters and whether this goal of the surgery can be achieved. The aim of this study was to assess potential differences of lower limb biomechanics during gait in patients following total hip replacement surgery depending on femoral head diameter and compare them to the normal gait of healthy volunteers. As a secondary outcome authors wanted to inspect correlation between gait parameters and patient-reported outcome.

NCT ID: NCT04496856 Completed - Sarcopenia Clinical Trials

Effects of Whey and Collagen on FFM, Muscle Strength and Wound Healing in Elderly Surgical Patients

Start date: May 10, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to compare the effect of whey protein and collagen on fat free mass, muscle strength, functional ability, wound healing and life quality in elderly patients undergoing elective knee- or hip surgery (defined as elective knee- or hip arthroplasty). The patients are admitted at the department of Orthopaedic Surgery at Herlev Gentofte Hospital.

NCT ID: NCT04026074 Completed - Knee Arthropathy Clinical Trials

Concepts for Analgosedation During Placement of Regional Anaesthesia Before Operations.

Start date: July 26, 2019
Phase: Phase 4
Study type: Interventional

Aim of the study is to specify the best analgosedation technique during placement of regional anaesthesia from the patients' view. In this double blind randomized trial the investigators will be testing the application of drugs administered intravenously (fentanyl-bolus, remifentanil-infusion, clonidine-bolus) or transcutaneously (EMLA salve) or placebo (NaCl 0,9% i.v. and skin protection salve).

NCT ID: NCT03900039 Completed - Clinical trials for Arthroplasty Complications

An Assessment of 4 Different Bearing Types in Hip Replacement Types to Analsye the Lowest Wear Rates of Polyethylene

Start date: July 26, 2005
Phase: N/A
Study type: Interventional

The aim of the study is to assess the ideal bearing surfaces in hip replacement by comparing 4 different combinations. In a hip replacement this means what the head and the socket liner are made of.

NCT ID: NCT03897387 Completed - Hip Arthritis Clinical Trials

Post Market, Retrospective Study to Evaluate Patients Implanted With Medacta Versafit Cup DM ™️ 2 Years Post-op

Start date: March 1, 2017
Phase:
Study type: Observational

This is a post-market, retrospective with one prospective visit, multi- center study, designed to assess the clinical outcomes, surgical details including Anterior or Posterior surgical approach, and collect all complication data of Medacta Versafit Cup DM used for primary or revision total hip arthroplasty at minimum two year post- operatively.

NCT ID: NCT03071250 Completed - Knee Osteoarthritis Clinical Trials

An Analysis of the Outcomes From Protocolized Perioperative Care for Patients Receiving Total Hip or Knee Arthroplasty

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

The care for patients receiving total hip and knee arthroplasty at the University of Arkansas for Medical Sciences has followed a structured care pathway since July 2015. This system of perioperative care has focused on preoperative assessment of medical co-morbidities and risks to postoperative functional recovery, anesthetic care focused on postoperative nausea and vomiting prevention and optimizing immediate postoperative functional ability, and aggressive postoperative physical therapy. This is an observational study to look at the outcomes of this program at University of Arkansas for Medical Sciences. Areas of focus will be hospital length of stay, postoperative narcotic consumption, Visual Analog Scale scores, incidence of postoperative nausea and vomiting, and 30-day readmission rates, and health literacy rates.