Clinical trials: Hip Replacement, Total
Total Hip Replacement, Coxarthrosis
Comparison of the Use of Conventional Ancillary Reaming and Single-use Ancillary Reaming Material in Total Hip Replacement
The main objective of the study is to compare the use of single-use ancillary reaming material during total hip replacement and conventional reusable ancillary reaming material.
- Trial name
- LUUC (NCT04903860)
- Testing
- total hip replacement with single use ancillary, total hip replacement with conventional ancillary
- Where
- France
- Volunteers
- 40 people
- Sponsor
- University Hospital, Clermont-Ferrand
Pain, Postoperative
Posterior Pericapsular Deep-gluteal Block
The goal of this clinical trial is to determine whether adding a posterior pericapsular deep-gluteal (PPD) block to pericapsular nerve group (PENG) and lateral femoral cutaneous nerve (LFCN) blocks improves pain control after…
- Trial name
- NCT07891013
- Testing
- PENG (Pericapsular nerve group) block, LFCN (Lateral femoral cutaneous nerve) block, PPD (Posterior pericapsular deep gluteal) block
- Volunteers
- 60 people
- Sponsor
- Ankara Etlik City Hospital
Arthroplasty, Recovery of Function
The Influence of Rapid Recovery on Sleep Quality Following Total Hip Replacement Surgery
To evaluate the influence of rapid recovery on sleep quality following total hip replacement surgery
- Conditions
- Arthroplasty, Recovery of Function, Sleep Quality
- Trial name
- NCT02852460
- Testing
- rapid recovery
- Where
- China
- Volunteers
- 170 people
- Sponsor
- Southwest Hospital, China
Osteoarthritis, Arthritis
A Multi-centre, Prospective Surveillance to Assess Mid-term Performance of the Mpact Cup
This is a multi-centre, prospective post marketing surveillance study to assess mid-term performance of the Mpact cup in subjects requiring primary total hip arthroplasty.
- Conditions
- Osteoarthritis, Arthritis, Avascular Necrosis, Fracture of the Femoral Neck or Head
- Trial name
- NCT02196818
- Testing
- Mpact Acetabular Shell
- Where
- 4 sites in United States
- Volunteers
- 200 people
- Sponsor
- Medacta International SA
Total Hip Arthroplasty (THA), Revision Hip Arthroplasty
Cementation of Cup and the Risk of Second Revision
Background: The fixation method of the acetabular component during the primary total hip arthroplasty (THA) affects the surgical techniques implemented in the revision surgery and may influence the risk of second revision.
- Trial name
- NCT06583382
- Volunteers
- 60,000 people
- Sponsor
- Bispebjerg Hospital
Osteoarthritis, Hip, Cardiovascular Diseases
Effects of Remote Ischaemic Preconditioning in Cemented Hip Arthroplasty.
Total joint arthroplasty is one of the best treatment options for end-stage osteoarthritis. Cemented hip arthroplasty is mainly indicated for elderly patients with poor bone quality and multiple comorbidities.
- Conditions
- Osteoarthritis, Hip, Cardiovascular Diseases, Bone Cement Implantation Syndrome, Kidney Diseases
- Trial name
- PRINCIPAL (NCT06323018)
- Testing
- Remote Ischemic Preconditioning
- Where
- Estonia
- Volunteers
- 200 people
- Sponsor
- University of Tartu
Arthroplasties, Hip Replacement
REDAPT Retrospective-Prospective Modular Stem Study
A Retrospective-Prospective Study of REDAPT Revision Femoral System Modular Stem is a post-market, retrospective-prospective, multi-center, single arm, consecutive series study design to provide data on the post market…
- Trial name
- NCT02661620
- Testing
- REDAPT Revision Femoral System modular stem
- Where
- 5 sites in United States, Belgium and 1 more
- Volunteers
- 140 people
- Sponsor
- Smith & Nephew, Inc.
Prosthesis-Related Infections, Hip Prosthesis Infection
Effect of Sonication on Periprosthetic Joint Infection Treatment Strategy.
It is not known in the literature how much sonication affects the patient's treatment. Another important issue is that the place of this method in diagnosis is not clear.
- Conditions
- Prosthesis-Related Infections, Hip Prosthesis Infection, Joint Infection, Biofilm
- Trial name
- NCT04304885
- Testing
- Sonication method
- Where
- Turkey (Türkiye)
- Volunteers
- 56 people
- Sponsor
- Bezmialem Vakif University
Osteoarthritis
Outcomes of Robotic Total Hip Arthroplasty
The objectives of this study are to evaluate the clinical value of robotic-assisted total hip arthroplasty with respect to acetabular cup implantation, and to document the long-term clinical outcome of patients with Total Hip…
- Trial name
- NCT01672320
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Massachusetts General Hospital
Dislocation, Hip
Dual Mobility Cup Versus Unipolar Cup
The general purpose of this study is to examine whether the dual mobility cup (Novae® Serf) reduces the number of hip dislocations after total hip replacement, both early dislocation (≤1 year) and late dislocation (>1 year) after…
- Trial name
- NCT04685239
- Testing
- dual mobility cup, unipolar cup
- Where
- Denmark
- Volunteers
- 1,000 people
- Sponsor
- Northern Orthopaedic Division, Denmark
Hip Osteoarthritis
Minimal Invasive Surgery in Total Hip Arthroplasty Patients; Short- and Long Term Results
The aim of the present study is to explore the most efficient surgical approach in total hip replacement in short and long term when concerning strength, functionality and postoperative complications.
- Trial name
- NCT01506024
- Testing
- Total hip arthroplasty direct lateral approach, Total hip arthroplasty posterior approach, Total hip arthroplasty, anterior approach
- Where
- Norway
- Volunteers
- 60 people
- Sponsor
- Norwegian University of Science and Technology
LOS, Postoperative Pain
Effects of Methylprednisolone After Total Hip Arthroplasty
The purpose of the study is to compare the effects of pre-operative methylprednisolone (125mg iv) versus placebo on postoperative outcome after hip arthroplasty.
- Conditions
- LOS, Postoperative Pain, Postoperative Nausea and Vomiting, Sleeping Quality
- Trial name
- NCT00968903
- Testing
- Methylprednisolone
- Where
- Denmark
- Volunteers
- 48 people
- Sponsor
- Hvidovre University Hospital
Analgesia
Analgesic Comparison of PENG/LFCN to FICB for Total Hip Arthroplasty
This study compares 2 commonly used interventions (regional pain blocks) used in hip arthroplasty for pain control. One of the interventions is newer and not widely established.
- Trial name
- PengvsFICB (NCT05477641)
- Testing
- Pericapsular Nerve Group Block with Lateral Femoral Cutaneous Nerve Block, Fascia Iliaca Compartment Block
- Where
- United States
- Volunteers
- 105 people, healthy volunteers welcome
- Sponsor
- SSM Health Bone and Joint Hospital at St Anthony
THA, Obesity
The Impact of Obesity on Short Stem Total Hip Arthroplasty
The purpose of this study is to review the impact of obesity on subsidence and clinical outcome after short stem total hip arthroplasty.
- Trial name
- NCT06430723
- Testing
- Total hip arthroplasty
- Where
- Austria
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Krankenhaus Barmherzige Schwestern Linz
Total Hip Arthroplasty (THA)
Comparison Between Opioid-sparing Anesthesia Guided by the CARDEAN® Index and Opioid-free Anesthesia During Total Hip Arthroplasty
The proposed study compares two anesthesia techniques; the hypothesis being tested is that titrating sufentanil based on the CARDEAN® index (titrated OSA) does not increase post-operative morphine consumption compared to…
- Trial name
- NCT07747142
- Testing
- Titrated Opioid Sparing Anesthesia, opioid free anesthesia
- Where
- France
- Volunteers
- 140 people
- Sponsor
- Pole Sante Oreliance, Polyclinique des Longues Allees
Total Hip Arthroplasty (THA)
MFinity BE Pre-market Trial
The primary objective of this trial is to determine the implant survival at 1 year of follow up in a population of patients undergoing primary Total Hip Replacement with MFinity Collared Femoral stem and to test its…
- Trial name
- NCT07616895
- Testing
- Mfinity collared stem
- Volunteers
- 95 people
- Sponsor
- Medacta International SA
Primary Total Hip Arthroplasty
Prospective Single-center Long-term Observation of the SL-PLUS® MIA Stem
Summary from initial protocol Goal: Validation of the uncoated SL-PLUS® MIA stem within an observation study Study design: prospective, single-center, observational, non-comparative study Study population: 135 consecutive cases…
- Trial name
- SL-PLUS MIA (NCT04122157)
- Volunteers
- 135 people, healthy volunteers welcome
- Sponsor
- Smith & Nephew Orthopaedics AG
Osteoarthritis, Hip
Mini Stem DEXA (Dual Energy X-ray Absorptiometry)
The objective of this study is to evaluate the bone ingrowth after implantation of the study device. This study will also document any device-related surgical complications or adverse radiographic observations.
- Trial name
- MISDexa (NCT01066936)
- Where
- Australia
- Volunteers
- 20 people
- Sponsor
- Smith & Nephew, Inc.
Hip Osteoarthritis
A Prospective Multi-center Study on Total Hip Arthroplasty With E1
The primary objectives of this clinical study include: Evaluate E1 Wear including early bedding-in process, clinical outcomes on patients who received Total Hip Arthroplasty with E1 Compare E1 wear used with CoCr and Biolox Delta…
- Trial name
- NCT01883492
- Testing
- Femoral Stem, Acetabular Cup, Acetabular Liner
- Where
- 5 sites in Japan
- Volunteers
- 153 people
- Sponsor
- Zimmer Biomet
Rehabilitation, Analgesia
Observational Prospective Study of Opiate-free Anesthesia for Anterior Total Hip Replacement
Opioid-free anesthesia (ATO) is a multimodal anaesthesia combining different analgesic and anesthetic modalities thus excluding opiates as an intraoperative.
- Conditions
- Rehabilitation, Analgesia, Anesthesia
- Trial name
- ASOPHA (NCT04112277)
- Testing
- Cumulative morphine consumption
- Where
- France
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Hôpital Privé Sévigné
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