Clinical trials: Hip Replacement Arthroplasty
Osteoarthritis
Clinical Study on BiHapro Total Hip System With Different Surface Coatings
This post market study intends to evaluate the safety and the performance of BiHapro Total Hip System with two types of coatings.
- Trial name
- NCT00755001
- Testing
- BiHapro hip stem with PPS Ti+Plasma HA, BiHapro hip stem with PPS Ti+BoneMaster HA
- Where
- 2 sites in Spain
- Volunteers
- 40 people
- Sponsor
- Zimmer Biomet
Osteoarthritis (OA) of the Hip
TED Stocking vs. Reparel Garment After Hip Replacement
This randomized, prospective study compares the effectiveness of a novel bioactive garment (Reparel Leg Sleeve) versus standard TED compression stockings in reducing postoperative leg swelling, pain, and deep vein thrombosis…
- Trial name
- NCT07246200
- Testing
- Reparel Bioactive Sleeve, TED Stocking
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Reparel
Empowerment
The Effects of Using the Empowerment Model Intervention in Primary Total Hip Replacement Surgery Elders
Degenerative arthritis is a common and serious chronic illness that impacts the quality of life of older adults. Knowledge about the effects of empowerment education program in older adults with total hip replacement surgery are…
- Trial name
- NCT02815163
- Testing
- Empowerment education
- Volunteers
- 108 people
- Sponsor
- Tzu-Ting Huang
Arthropathy of Hip
Clinical Analysis of Suction Drainage in Cementless Hip Replacement
Randomized prospective study assessing suction drainage in total hip arthroplasty. Group without drainage, 50 hips, compared with group with suction drainage, 50 hips.
- Trial name
- NCT04333264
- Testing
- suction drainage, no suction drainage
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Bartosz Paweł
Blood Loss, Surgical
Oral Tranexamic Acid vs. Oral Aminocaproic Acid to Reduce Blood Loss After Total Hip Replacement
This study compares two oral medications (tranexamic acid and aminocaproic acid) as hemostatic agent administered in patients undergoing primary total hip replacement
- Trial name
- NCT04187014
- Testing
- Aminocaproic Acid 1000Mg Tab, Tranexamic acid tablets
- Where
- Mexico
- Volunteers
- 90 people
- Sponsor
- Carlos A Acosta-Olivo
Arthroplasty Complications, Muscle Weakness
Achilles Tendon for the Treatment of Gluteus Medius Insufficiency
Residual limping after total hip arthroplasty is a serious complication that lacks effective treatment. The purpose of this study is to evaluate a surgical treatment for residual limping and compare its results with non-surgical…
- Conditions
- Arthroplasty Complications, Muscle Weakness, Muscle Atrophy, Muscle Tear
- Trial name
- HLS (NCT05206838)
- Testing
- Surgical reconstruction of gluteus medius with Achilles tendon allograft
- Where
- Sweden
- Volunteers
- 44 people
- Sponsor
- Sahlgrenska University Hospital
Postoperative Cognitive Dysfunction
Postoperative Cognitive Dysfunction After Total Knee or Hip Replacement Surgery in Fast-track Set-up
The aim of this study is to quantify the incidence of postoperative cognitive dysfunction in the elderly patient (>60y) after total hip or knee replacement surgery.
- Trial name
- NCT01103752
- Testing
- no intervention, descriptive study
- Where
- Denmark
- Volunteers
- 225 people, healthy volunteers welcome
- Sponsor
- Lene Krenk
Total Hip Replacement
Digital Healthcare App After Total Hip Arthroplasty
This study examines the effectiveness of rehabilitation after hip replacement surgery using a specialised app called Akina Cloud. Medical professionals at the Schulthess Clinic will provide detailed information about the study.
- Trial name
- NCT06409312
- Testing
- Akina Cloud
- Volunteers
- 20 people
- Sponsor
- Schulthess Klinik
Improve Quality of Life
Exercise Program After Total Hip and Knee Replacement: a Randomized Controlled Trial
Randomized controlled trial. Patients will be enrolled at the moment of the pre-surgery assessment after verifying the inclusion/exclusion criteria and signing written informed consent.
- Trial name
- PAIR (NCT04761367)
- Testing
- Physical activity. Physical Activity program is performed in a group in a gym
- Where
- Italy
- Volunteers
- 42 people
- Sponsor
- Istituto Ortopedico Rizzoli
Total Knee Arthroplasty
Biological Link Between Anxiety and Outcomes Post Knee Arthroplasty
This is a single-site, observational pilot study that aims to understand whether there is a biological explanation for why some patients with anxiety or depression experience poorer outcomes after total knee or hip replacement…
- Trial name
- NCT07102563
- Where
- United Kingdom
- Volunteers
- 56 people
- Sponsor
- Robert Jones and Agnes Hunt Orthopaedic and District NHS Trust
Acetabular Abnormality
Outcomes of Trabecular Metal Augments Used in the Flying Buttress Position
This study hypothesize that trabecular metal augments used in the flying buttress position is a valid option with good results in the management of uncontained acetabular defects.
- Trial name
- NCT06678958
- Testing
- Reconstruction of acetabular defect by trabecular metal augment
- Volunteers
- 30 people
- Sponsor
- Ain Shams University
Arthroplasty Total Hip Replacement
The Relationship Between Operative and Radiologic Stem Version
Investigators prospectively evaluate the accuracy of intraoperative stem anteversion in 40consecutive total hip arthroplasties.
- Trial name
- NCT02552173
- Testing
- The Relationship Between Operative and Radiologic Stem Version
- Where
- South Korea
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Seoul National University Bundang Hospital
Arthroplasty Complications
Are Elastic Restraints Still Necessary in Improved Rehabilitation Programs After Hip and Knee Prosthetic Surgery?
Venous thrombosis and pulmonary embolism are considered serious and potentially preventable complications of hip and knee replacement surgery.
- Trial name
- NCT06563531
- Testing
- Pharmacological thromboprophylaxis and elastic compression, Pharmacological thromboprophylaxis without elastic compression
- Where
- France
- Volunteers
- 1,274 people
- Sponsor
- Clinique Pasteur Lanroze
Total Hip Replacement Surgery, Postoperative Pain
Effectiveness of PENG Block Combined to LFCN Block on the Quality of Recovery After Total Hip Replacement
The main objective of this study is to evaluate the effectiveness of the association of PENG and LFCN blocks on the quality of recovery 24 hours after total hip replacement surgery.
- Trial name
- PENG (NCT04245280)
- Testing
- Ropivacaine 0.5% Injectable Solution, Saline Solution
- Where
- Canada
- Volunteers
- 74 people
- Sponsor
- Centre hospitalier de l'Université de Montréal (CHUM)
Hip Osteoarthritis, Hip Arthroplasty Replacement
Virtual Reality for Intraoperative Anxiolysis and Postoperative Agitation in Elderely Hip Arthroplasty Patients
This study evaluates the effectiveness of Virtual Reality (VR) as a non-pharmacological intervention to reduce intraoperative anxiety and postoperative agitation in elderly patients undergoing elective hip arthroplasty under…
- Conditions
- Hip Osteoarthritis, Hip Arthroplasty Replacement, Emergence Delirium, Anesthesia, Emergence Agitation
- Trial name
- VR (NCT07705451)
- Testing
- immersive virtual reality, standard sedation
- Volunteers
- 40 people
- Sponsor
- Menoufia University
Acute or Programmed Hip Replacement (Gamma Nail, Total Prosthesis or Throuhg DHS) / Knee Surgery
Assessment of Blood Loss With a Point Of Care Device
Main Objective: The purpose of this study is to demonstrate whether there is a correlation between perioperative blood loss and the degree of platelet inhibition assessed by a point of care assay in patients undergoing hip or…
- Trial name
- BLOOD (NCT01430273)
- Where
- 3 sites in France
- Volunteers
- 28 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Periprosthetic Fractures
Locking Compression Plate Fixation Versus Revision- Prosthesis of Vancouver-B2, B3 and C Periprosthetic Femoral Fractures After Total Hip Replacement
The purpose of this study was to compare the clinical (range of motion, weight bearing, quality of life) and radiographic outcome (boney consolidation) between open reduction and internal fixation using locking compression plates…
- Trial name
- NCT02391129
- Testing
- Operation for Periprosthetic fractures of the hip with stem loosening
- Volunteers
- 102 people
- Sponsor
- Medical University of Vienna
Osteoarthritis
Overcoming TWEAK Signaling to Restore Muscle and Mobility After Joint Replacement
This single-blind, randomized, controlled trial is designed to test the effect of an intensive, 16 week exercise rehabilitation program (progressive resistance training + functional mobility training) vs.
- Trial name
- TWEAK (NCT02628795)
- Testing
- PRT + FM, Usual Care
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- University of Alabama at Birmingham
PENG Block
Efficacy of Dexmedetomidine As an Adjuvant to Bupivacaine in Pericapsular Nerve Group Block in Hip Replacement Surgeries
Our aim will be to investigate the efficacy of dexmedetomidine as an adjuvant to bupivacaine in ultrasound guided pericapsular nerve group (PENG) block for postoperative analgesia in hip replacement surgeries.
- Trial name
- NCT06736392
- Testing
- Ultrasound guided Pericapsular Nerve Group Block, Isobaric Bupivacaine 0. 25%, 20 ml isobaric bupivacaine 0.25% and 1.5μg/kg dexmedetomidine
- Volunteers
- 60 people
- Sponsor
- Assiut University
Arthroplasty
Efficacy and Safety Study of 4975 in Patients Undergoing Total Hip Replacement
Evaluate the efficacy, safety and tolerability of a single intraoperative dose of 4975 in patients undergoing total hip replacement
- Trial name
- NCT00683267
- Testing
- 4975, highly purified capsaicin
- Where
- 10 sites in United States
- Volunteers
- 118 people
- Sponsor
- Anesiva, Inc.