Clinical trials: Hip Replacement, Total
PreDiabetes
Digital Diabetes Prevention Program Study
The aim of this study is to determine if completion of the Diabetes Prevention Program (DPP) via the Transform 10 website can significantly decrease hemoglobin A1c (HbA1c) levels and Body Mass Index (BMI) in prediabetic…
- Trial name
- NCT06137963
- Testing
- Transform10 Diabetes Prevention Program
- Where
- United States
- Sponsor
- Hospital for Special Surgery, New York
Hip and Knee Prosthesis Implantation
Aspirin Thromboprophylaxis After First-line Total Hip and Knee Replacement
Annually, more than 100,000 total hip prostheses (THA) and more than 100,000 total knee prostheses (TKA) are implanted for osteoarthritis in France, and these figures are set to increase significantly in the future as in all…
- Trial name
- TBP-ASPIR (NCT05128214)
- Where
- France
- Volunteers
- 200 people
- Sponsor
- University Hospital, Strasbourg, France
Hip Arthropathy, Knee Arthropathy
Effect of Vitamin D Status and Repletion on Postoperative Total Joint Arthroplasty Complications
Vitamin D status has been shown to have an effect on post-operative outcomes in total joint arthroplasty. The goal of this study is to determine if pre-operative supplementation and correction of Vitamin D deficiency can reduce…
- Conditions
- Hip Arthropathy, Knee Arthropathy, Vitamin D Deficiency
- Trial name
- NCT04229368
- Testing
- Vitamin D3
- Where
- United States
- Volunteers
- 900 people
- Sponsor
- Brigham and Women's Hospital
Osteoarthrosis Patients With Total Hip Arthroplasty
Thigh Swelling, Hip-muscle Strength, and Functional Performance Following Total Hip Arthroplasty
By this study the investigators wish to (1) quantify hip strength and functional-performance deficits at discharge after fast-track total hip arthroplasty (THA), and (2) investigate if changes in thigh circumferences, or hip pain…
- Trial name
- THA (NCT01246674)
- Where
- Denmark
- Volunteers
- 30 people
- Sponsor
- Hvidovre University Hospital
Total Hip Arthroplasty
Post Market Clinical Follow-Up of Plasmafit® Cup
Twelve months follow-up of implant survival and clinical and radiological follow-up of Plasmafit® Cup.
- Trial name
- NCT02019849
- Testing
- Plasmafit® Total Hip Arthroplasty
- Where
- 2 sites in Germany
- Volunteers
- 100 people
- Sponsor
- Aesculap AG
Non-inflammatory Degenerative Joint Disease, Osteoarthritis
Ceramic On Ceramic (COC) 36mm PAS IDE Rollover Subjects; Ceramic Acetabular Bearing With Ceramic Femoral Head in Total Hip Replacement
This study is intended to gather medium (5- to 7-years) and long-term (minimum 8- to 10-years) information regarding the performance and safety of the commercially available 36mm CERAMAX® Ceramic on Ceramic (COC) Total Hip System…
- Conditions
- Non-inflammatory Degenerative Joint Disease, Osteoarthritis, Avascular Necrosis, Post-Traumatic Osteoarthritis of Hip
- Trial name
- COC36mmPAS (NCT02096198)
- Where
- 5 sites in United States
- Volunteers
- 81 people
- Sponsor
- DePuy Orthopaedics
Total Hip Replacement
Postoperative Analgesia After Total Hip Replacement
There are several treatments for postoperative pain after Hip Replacement Surgery. However, some require an intravenous line which may interfere with rehabilitation after surgery.
- Trial name
- NCT00219921
- Testing
- intrathecal morphine AND patient controlled analgesia with iv morphine
- Volunteers
- 120 people
- Sponsor
- Rijnstate Hospital
Arthroplasty, Replacement, Coagulation Factors
An Evaluation of Clotting Factor Activity Before and After Total Hip Arthroplasty
The objective of the study was to analyze both the concentration and the activity of the clotting factors, D-dimer levels, as well as fibrinogen concentration in patients who underwent primary total hip arthroplasty due to…
- Trial name
- CloFaTHA (NCT04372173)
- Testing
- analysis of the concentration of the clotting factors in patients who underwent primary hip arthroplasty
- Where
- Poland
- Volunteers
- 30 people
- Sponsor
- Military Institute od Medicine National Research Institute
Total Hip Arthroplasty
A Hemodynamic Comparison of Stationary and Portable Pneumatic Compression Devices
We are comparing two pneumatic compression devices, VenaFlow (stationary) and MCS (portable) in both the supine an standing position.
- Trial name
- NCT02345642
- Testing
- ActiveCare+SFT Supine, VenaFlow Elite Supine, ActiveCare+SFT Standing
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Hospital for Special Surgery, New York
Pain, Postoperative
Effect of Paracetamol, Pregabalin and Dexamethasone on Pain and Opioid Requirements in Patients After Hip Operations
Patients scheduled for primary total hip replacement needs postoperative pain treatment: i.e. morphine. Unfortunately morphine has side-effects: nausea, vomiting, sedation and dizziness, which is unpleasant for the patients and…
- Trial name
- NCT00235261
- Testing
- Pregabalin, Dexamethasone
- Where
- Denmark
- Volunteers
- 120 people
- Sponsor
- Glostrup University Hospital, Copenhagen
Gait Analysis, Hip Fractures
Gait Pattern Between a Cemented and Non-cemented Femur Stem
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…
- Conditions
- Gait Analysis, Hip Fractures, Hip Arthroplasty, Randomized
- Trial name
- NCT04791605
- Testing
- Gait analysis
- Where
- Sweden
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Göteborg University
Venous Thromboembolism, Venous Thromboses
inDividual, Targeted thrombosIS Prophylaxis Versus the Standard 'One Size Fits All' Approach in Patients Undergoing Total hIp or Total kNee replaCemenT
After hip or knee replacement all patients receive a standardized treatment with blood thinners, this medication is called thrombosis prophylaxis.
- Conditions
- Venous Thromboembolism, Venous Thromboses, Pulmonary Embolism, Deep Vein Thrombosis
- Trial name
- DISTINCT (NCT06581965)
- Testing
- Short duration prophylaxis, Higher intensity and longer duration prophylaxis, Control
- Where
- 13 sites in Netherlands
- Volunteers
- 10,078 people
- Sponsor
- Leiden University Medical Center
The Results of Total Hip Arthroplasty in Crowe Type 4 Dysplastic Hips
The Results of Total Hip Arthroplasty in Crowe Type 4 Hips.
Total hip arthroplasty (THA) performed for developmental dysplasia of the hip (DDH) is a technically difficult procedure with a high complication rate, especially in the presence of completely dislocated hips.
- Trial name
- NCT04834492
- Testing
- Total hip arthroplasty
- Where
- Turkey (Türkiye)
- Volunteers
- 67 people
- Sponsor
- Private Ortopedia Hospital, Seyhan Adana
Surgical Education, Operating Room Nursing
Digital Gamification vs. Traditional Training for Hip Replacement Instrument Table Setup (ORNurse)
This randomized controlled trial aims to compare the effectiveness of a digital gamification-based training method and a traditional training method on instrument table layout skills in total hip replacement surgery.
- Conditions
- Surgical Education, Operating Room Nursing, Educational Technology
- Trial name
- ORNurse (NCT07194148)
- Testing
- Gamified Digital Education (ORNurse: Steril Setup 1.0), Traditional Training
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- DERYA ESENKAYA
Osteoarthritis, Hip
Evaluation of Functional Rehabilitation in Patients Undergoing Physiotherapy After Total Hip Arthroplasty
This study aims to objectively evaluate the implications of physiotherapeutic rehabilitation in the Assistance Protocol of Total Hip Arthroplasty (THA), by assessing the motor performance and testing the quality of life of…
- Trial name
- Artrhosis (NCT01491048)
- Testing
- THA Physiotherapy, No physiotherapy after THA
- Where
- Brazil
- Volunteers
- 104 people, healthy volunteers welcome
- Sponsor
- Hospital de Clinicas de Porto Alegre
Arthroplasty
ThromboEmbolism Prevention Efficacy and Safety Trial (TEMPEST)
The purpose of this study is to gain additional safety information as well as to determine after the study drug has been given to patients who have undergone total hip replacement surgery, whether the study drug is effective in…
- Trial name
- TEMPEST (NCT00041509)
- Testing
- SB-424323
- Volunteers
- 343 people
- Sponsor
- GlaxoSmithKline
Total Hip Replacement
Evaluation of X-ray, Acetabular Guides and CT in THR
Total hip replacement is one of the most successful surgical procedures of modern times, with over 80,000 performed each year in the UK.
- Trial name
- EXACT (NCT03072706)
- Testing
- Corin OPS™, 2D X-ray templating technology
- Where
- United Kingdom
- Volunteers
- 54 people
- Sponsor
- University Hospitals Coventry and Warwickshire NHS Trust
Hip Osteoarthritis, Postoperative Pain
Total Periarticular Infiltration Vs Posterior Periarticular Infiltration Plus PENG Block for Hip Analgesia
In a recent study, direct periarticular local anesthetic infiltration (PAI) showed a greater incidence of early quadriceps weakness (33% at 3 hours and 13% at 6 hours) than pericapsular nerve group block (PENGB) in total hip…
- Trial name
- NCT06075004
- Testing
- Periarticular Local Anesthetic Infiltration, Posterior Periarticular Local Anesthetic Infiltration plus Pericapsular Nerve Group Block
- Where
- Chile
- Volunteers
- 74 people
- Sponsor
- University of Chile
Osteoarthritis, Arthroplasty
Psoas Compartment Block Versus Periarticular Local Anesthetic for Total Hip Arthroplasty
The primary objective of this study is to examine whether there is a difference in the level of resting pain following total hip arthroplasty with an anterior approach with use of a psoas compartment block versus a local…
- Trial name
- NCT02658149
- Testing
- Ropivacaine with NaCl, Epinephrine, Morphine
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Corewell Health East
Postoperative Pain, Total Hip Arthroplasty (THA)
PENG Block With or Without PPD Block for Postoperative Analgesia After Total Hip Arthroplasty
This single-center, prospective, randomized controlled clinical trial aims to compare the postoperative analgesic efficacy of PENG block with or without posterior pericapsular deep gluteal block in adult patients undergoing…
- Trial name
- NCT07502248
- Testing
- PENG Block, Deep posterior gluteal compartment block
- Volunteers
- 40 people
- Sponsor
- Kirsehir Ahi Evran Universitesi
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