Clinical trials: Hip Joint Disorders
Osteoarthritis of the Hip
Physical Therapy Prior to Total Knee Replacement
In this study, the investigators are investigating the effects of physical therapy (PT) for treating high grade knee osteoarthritis (OA) in patients that are candidates for total knee replacement.
- Trial name
- NCT02279277
- Testing
- Supervised physical therapy program prior to total knee replacement surgery
- Volunteers
- 148 people
- Sponsor
- Rothman Institute Orthopaedics
Femoroacetabular Impingement, Hip Developmental Dysplasia
Cross-sectional Study of Ultrasonic Diagnosis of Iliac Joint Capsule Muscle
In order to investigate the relationship between the iliac joint capsular muscle and the development of the hip joint, this study used ultrasound Doppler to measure the anatomical circumference of the iliac joint capsular muscle…
- Trial name
- NCT04968301
- Testing
- ultrasound Doppler
- Where
- China
- Volunteers
- 132 people, healthy volunteers welcome
- Sponsor
- Peking University Third Hospital
Regional Anesthesia Morbidity, Arthropathy of Hip
Comparison of PENG Associated with LFCN Block Versus FICB for Multimodal Analgesic Management in THA
Optimal pain control with limited muscle weakness is paramount for a swift initiation of physical therapy and ambulation. Fascia iliaca compartment block (FIC) has been recommended since it offers the best pain control with low…
- Conditions
- Regional Anesthesia Morbidity, Arthropathy of Hip, Hip Arthropathy, Post Operative Pain
- Trial name
- NCT06147401
- Testing
- PENG plus LFCN block, FIC Block
- Where
- Italy
- Volunteers
- 58 people
- Sponsor
- Ospedale Edoardo Bassini
Arthroplasty, Replacement, Knee, Rehabilitation
Patient Reported Outcome Measures (PROMs) in Rehabilitation With or Without the Possible Use of a Mobile Application After Primary Knee or Hip Arthroplasty
Rehabilitation after primary knee or hip arthroplasty may include performing exercises with a physiotherapist. For patients who can work well with a computer, tablet or smartphone, it is now possible to use a mobile application…
- Conditions
- Arthroplasty, Replacement, Knee, Rehabilitation, Hip Arthrosis
- Trial name
- NCT04628468
- Testing
- moveUp, Predefined number of traditional physiotherapy sessions
- Where
- 11 sites in Belgium
- Volunteers
- 416 people
- Sponsor
- University Hospital, Ghent
Hip Osteoarthritis, Arthroplasty, Replacement, Hip
Expectations, Satisfaction and Quality of Life in Total Hip Arthroplasty
The goals of this study are to identify predictors of improvement in quality of life and satisfaction with total hip arthroplasty three to five years after surgery.
- Trial name
- NCT00197990
- Where
- United States
- Volunteers
- 405 people
- Sponsor
- Hospital for Special Surgery, New York
Osteoarthritis, Knee, Osteoarthritis, Hip
The Effect of ColcHicine on the Incidence of Knee or Hip Replacements
The goal of this clinical trial is to evaluate the effect of treatment with colchicine 0.5mg once daily as compared to placebo in patients with knee or hip osteoarthritis on the incidence of first occurrence of knee or hip…
- Trial name
- ECHO (NCT06578182)
- Testing
- Colchicine
- Where
- Netherlands
- Volunteers
- 1,410 people
- Sponsor
- Sint Maartenskliniek
Femoroacetabular Impingement, Chondral Lesions
Efficacy of PRP (Platelet Rich Plasma) Following Arthroscopic Microfracture of Chondral Lesions of the Hip
The purpose of this research project is to assess the effectiveness of intra-articular injections of autologous platelet-rich plasma (PRP) after arthroscopic microfracture.
- Trial name
- NCT02183896
- Testing
- Platelet-rich plasma (PRP), Saline
- Where
- United States
- Sponsor
- University of Colorado, Denver
Hip Arthropathy, Hypothermia
Rectal Temperature Measurement in Detecting Hypothermia During Hip Arthroscopy
Irrigation fluids used during hip arthroscopy surgery are generally stored at room temperature and are cooler than the core temperature of the patient. They are used abundantly during hip arthroscopy surgery.
- Conditions
- Hip Arthropathy, Hypothermia, Orthopedic Disorder
- Trial name
- NCT05396924
- Testing
- Rectal temperature measurement, Temporal temperature measurement
- Where
- Turkey (Türkiye)
- Volunteers
- 116 people
- Sponsor
- Ankara City Hospital Bilkent
HIP AND KNEE OSTEOARTHRITIS
Prepare II - Predictive Model Training and External Validation
The general aim of the project is training and testing a predictive model of inpatient rehabilitation stay after hip and knee replacement for osteoarthritis.
- Trial name
- NCT07304323
- Testing
- Functional rehabilitation
- Where
- Italy
- Volunteers
- 400 people
- Sponsor
- I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Hip Osteoarthritis
Dynamic ROM Via Gait Analysis and 3D Fluoroscopy in THA With Different Head Diameters
Pain and reduced function are the most common symptoms of coxarthritis. Pain relief and normal range of motion (ROM) restoration are the objectives of a Total Hip Arthroplasty (THA) procedure.
- Trial name
- DROMDP (NCT02047292)
- Testing
- THA Corail PinnacleCoC28, THA Corail DeltaMotion36, THA Corail DeltaMotion40
- Where
- Italy
- Volunteers
- 30 people
- Sponsor
- Istituto Ortopedico Rizzoli
Hip Osteoarthritis, Hip Pain Chronic
PENG Block Variants With Dexamethasone and Dexmedetomidine in Older Adults
This study will compare three different versions of the Pericapsular Nerve Group (PENG) block in adults aged 65 years and older who are undergoing surgery for hip conditions.
- Trial name
- NCT07327931
- Testing
- Dexamethasone (intravenous), Dexamethasone (intravenous) with Dexmedetomidine (perineural), Dexamethasone (perineural) with Dexmedetomidine (perineural)
- Where
- Poland
- Volunteers
- 120 people
- Sponsor
- Poznan University of Medical Sciences
Fractures, Bone, Stroke
Tele-Rehabilitation Pilot Evaluation Study
A proof of concept randomized controlled trial (RCT) only evaluated the National University of Singapore's (NUS) T-Rehab tele-rehabilitation (TR) system at a home setting where rehabilitation was provided on an individual level.
- Conditions
- Fractures, Bone, Stroke, Lower Limb Joint Replacement (Hip or Knee), Lower Limb Amputation
- Trial name
- NCT03409354
- Testing
- Tele-rehabilitation, Usual care
- Where
- Singapore
- Volunteers
- 14 people
- Sponsor
- National University of Singapore
Osteoarthritis
A Qualitative Investigation of CLEAT Participants
As the United Kingdom's National Health Service (NHS) waiting list soars above seven million people, with treatment wait times over two years, older people with chronic conditions face worsening symptoms, increased use of…
- Trial name
- NCT05937542
- Testing
- Qualitative Investigation of Participant Experiences
- Where
- United Kingdom
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Bournemouth University
Coxarthrosis
The Influence of Global Femoral-offset Changes After Total Hip Arthroplasty
The femoral-offset (FO) is one of the important perioperative parameters in THA. A prospective cohort study was conducted between September 2010 and December 2013.
- Trial name
- NCT02399670
- Volunteers
- 222 people
- Sponsor
- Sundsvall Hospital
Hip Osteoarthritis
Evaluation of a New Coating in Cement Less Femoral Stems
The purpose of this trial is to evaluate a new method of applying hydroxyapatite coatings on cement-less femoral stems.
- Trial name
- NCT02321683
- Testing
- Taperloc
- Volunteers
- 55 people
- Sponsor
- Lars Nordsletten
Osteoarthritis, Hyperthyroidism
Povidone Iodine Irrıgation at Hip-Knee Arthroplasty
Povidone iodine (PI) solution is an antimicrobial solution that can be used at hip and knee arthroplasty cases. It contains iodine that may be absorbed by the body.
- Conditions
- Osteoarthritis, Hyperthyroidism, Iodine Toxicity
- Trial name
- NCT05599841
- Testing
- PI solution, Saline Solution
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people
- Sponsor
- Ankara University
Osteolysis, Arthroplasty Complications
Plasmafit® Revision Structan® Hip Endoprosthesis Cup
The aim of this observational study is to collect clinical and radiological results of the new Plasmafit® Revision Structan® Hip Endoprosthesis Cup in a standard patient population and when used in routine clinical practice.
- Conditions
- Osteolysis, Arthroplasty Complications, Instability of Prosthetic Joint, Degenerative Osteoarthritis
- Trial name
- NCT04255966
- Testing
- Plasmafit® Revision Structan®
- Where
- 4 sites in Germany
- Volunteers
- 60 people
- Sponsor
- Aesculap AG
Hip Osteoarthritis, Noninflammatory Degenerative Joint Disease
Randomized Controlled RSA Study Comparing the Taperloc Complete Versus the Taperloc Complete Microplasty.
This is a single center, prospective, randomized controlled study. The primary objective of this study is to measure migration over two years with RSA.
- Conditions
- Hip Osteoarthritis, Noninflammatory Degenerative Joint Disease, Avascular Necrosis, Correction of Functional Deformity
- Trial name
- NCT03409666
- Testing
- Taperloc Complete Microplasty stem, Taperloc Complete Reduced Distal stem
- Where
- Netherlands
- Volunteers
- 50 people
- Sponsor
- Zimmer Biomet
Hip Osteoarthritis, Heterotopic Ossification
Balance in Patients With Ectopic Bone Tissue After Total Hip Replacement
One of the typical complications which occurs after total hip replacement (THR) procedure is heterotopic ossification (HO). According to current studies abnormal formation of bone after trauma or replacement of the hip could…
- Conditions
- Hip Osteoarthritis, Heterotopic Ossification, Hip Arthropathy
- Trial name
- NCT05218954
- Testing
- Biomechanical analysis of risk fall
- Where
- Poland
- Volunteers
- 88 people
- Sponsor
- Medical University of Warsaw
Arthropathy of Knee, Arthropathy of Hip
Does the Use of Intrathecal Morphine Increase the Length of Hospital Stay in Fast Track Orthopedic Procedures?
This is a clinical trial of intrathecal morphine for patients Patient with primary as well as revision knee and hip arthroplasty under regional anesthesia. This study would include a total of 134 patients.
- Trial name
- NCT05105074
- Testing
- Intrathecal Morphine
- Where
- Canada
- Volunteers
- 104 people, healthy volunteers welcome
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital
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