Clinical trials: Hip Replacement, Total
Total Hip Arthroplasty for Osteoarthritis
Analgesia for Total Hip Arthroplasty With PENG Block (ATHAPENG)
Analgesia for Total Hip Arthroplasty with PENG block (ATHAPENG)
- Trial name
- ATHAPENG (NCT06954207)
- Testing
- Non interventional. Data collection concerns routine procedures and monitoring devices
- Where
- France
- Volunteers
- 70 people
- Sponsor
- Hospices Civils de Lyon
Primary Total Hip Arthroplasty
Accuracy of OPS™ Femoral Neck Resection Study
The primary objective of this study is to determine the accuracy of the Optimized Positioning System (OPS™) planning and delivery tools using different types of surgical approaches.
- Trial name
- NCT03956381
- Testing
- Primary Total Hip Replacement with Trinity cup and TriFit TS stem via posterolateral surgical approach., Primary Total Hip Replacement with Trinity cup and MetaFix stem via direct anterior surgical approach
- Where
- United States
- Volunteers
- 55 people
- Sponsor
- Corin
Pain, Postoperative, Ropivacaine
Effect of Nervus Cutaneous Femoris Lateralis-Blockade on Moderate Pain Responders After Total Hip Arthroplasty
The patients will be included the 1. or 2. day after surgery. All THA patients will be screened. Those reporting VAS > 40 during active 30 degrees hip flexion will be asked to participate.
- Conditions
- Pain, Postoperative, Ropivacaine, Therapeutic Use, Arthroplasty, Replacement, Hip
- Trial name
- NCT02344264
- Testing
- Ropivacaine, Saline
- Where
- Denmark
- Volunteers
- 60 people
- Sponsor
- Daniel Hägi-Pedersen
Postoperative Cognitive Dysfunction, Chronic Post Operative Pain
Chronic Postsurgical Pain, Postoperative Cognitive Dysfunction and Resilience
"Brain damage" and "memory loss" are main concerns of people undergoing surgery. In fact, many older people undergoing different types of non-cardiac surgeries (including orthopedic surgeries) present a significant decline in…
- Conditions
- Postoperative Cognitive Dysfunction, Chronic Post Operative Pain, Satisfaction, Patient, Coping Behavior
- Trial name
- ArthroCaP (NCT05614271)
- Where
- Canada
- Volunteers
- 100 people
- Sponsor
- McMaster University
Venous Thromboembolism
Rivaroxaban (10mg) Given Once Daily in Patients Undergoing Total Hip Replacement Compared to Enoxaparin
The purpose of this study is to assess if 10 mg BAY 59-7939, taken once daily as a tablet, is safe and prevent blood clot which may form after total hip replacement operation.
- Trial name
- NCT00329628
- Testing
- Rivaroxaban (BAY59-7939), Enoxaparin
- Where
- 215 sites in United States, Argentina and 26 more
- Volunteers
- 4,541 people
- Sponsor
- Bayer
Arthropathy, Obesity
Postoperative BMI Changes and Functional Outcomes in Knee and Hip Arthroplasty
PURPOSE Obesity poses challenges to preoperative mobility and functional recovery for arthroplasty patients, yet postoperative weight loss remains elusive.
- Trial name
- NCT06440863
- Testing
- Total Knee Arthroplasty, Total Hip arthroplasty
- Where
- Turkey (Türkiye)
- Volunteers
- 459 people
- Sponsor
- Istanbul University - Cerrahpasa
Periprosthetic Infection Total Hip Arthoplasty
Treatment of Acute Periprosthetic Total Hip Arthroplasty Infections
The purpose of this study is to determine the success rate of two treatments for infection after total hip replacement: single stage arthroplasty exchange (your surgeon will take out your original implants and replace them with a…
- Trial name
- NCT01712880
- Testing
- open debridement with modular exchange, one stage exchange
- Where
- United States
- Sponsor
- OrthoCarolina Research Institute, Inc.
Total Hip Arthroplasty (THA)
Lumbal Erector Spinae Plane Block for Pain Management After Total Hip Arthroplasty
The Erector Spinae Plane (ESP) block or spinal erector block was first described in September 2016 by a Canadian team. It's a block that was initially used for the treatment of chronic thoracic neuropathic pain.
- Trial name
- NCT07240961
- Testing
- Lumbal Erector Spinae Plane Block, intravenous pain killers
- Where
- Tunisia
- Volunteers
- 60 people
- Sponsor
- University Tunis El Manar
Osteoarthitis, Sacro Iliac Joint Pain
PRP Injection Into the Sacroiliac Joint After Ipsilateral THA: Effects on Early Recovery and Function (SIJ-THA Randomized Trial)
The study is an interventional, randomized, open-label (non-blinded), placebo-controlled trial. Preoperatively, patients scheduled for primary total hip arthroplasty (THA) will undergo a clinical examination in the Orthopaedic…
- Conditions
- Osteoarthitis, Sacro Iliac Joint Pain, Hip Arthroplasty, Total, Sacro-Iliac Spondylosis
- Trial name
- NCT07498660
- Testing
- PRP injection
- Where
- Poland
- Volunteers
- 60 people
- Sponsor
- Medical University of Warsaw
Pertrochanter Fracture
Pertrochanter Arthroplasty Versus Osteosynthesis
This is a single-centre, comparative, prospective randomised trial. It will include 70 patients over a period of 2 years randomized into two groups of 35 patients: one group of patients treated with osteosynthesis (plate, nail or…
- Trial name
- PAVO (NCT02171897)
- Testing
- Osteosynthesis, Total hip replacement
- Where
- France
- Volunteers
- 70 people
- Sponsor
- Centre Hospitalier Universitaire Dijon
Hip Osteoarthritis
Prospective Clinical Follow-up of the Echo Bi-Metric Microplasty Stem for Total Hip Arthroplasty
The primary objective of this study is to characterize survivorship of the Echo Bi-Metric Microplasty stem in unilateral or bilateral primary total hip arthroplasty at 5 years postoperative.
- Trial name
- NCT04326010
- Testing
- Surgery
- Where
- 6 sites in United States
- Volunteers
- 206 people
- Sponsor
- Zimmer Biomet
Arthroplasty, Replacement
Comparison of Metal on Metal Total Hip Arthroplasty and Metal on Metal Total Hip Resurfacing.
The goal of this double-blind prospective randomized study is to compare subjective outcome measures and gait parameters between conventional THA using large diameter femoral heads and total hip resurfacing
- Conditions
- Arthroplasty, Replacement, Hip
- Trial name
- NCT04516239
- Testing
- THA, HR
- Volunteers
- 48 people
- Sponsor
- Ciusss de L'Est de l'Île de Montréal
Osteoarthritis of the Hip
Efficacy of Preoperative Education and Mini-invasive Surgery for Total Hip Replacement
We propose to evaluate a preoperative education of the patient and a new surgical technique (the mini-invasive THR) that could reduce the time to achieve functional independence.
- Trial name
- ANRACT (NCT00449228)
- Testing
- -preoperative education and total hip replacement
- Where
- France
- Volunteers
- 215 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Arthropathy of Knee, Osteo Arthritis Knee
Meditation and Opioid Consumption in Total Joint Replacement Patients Undergo Primary Total Hip and Knee Replacement
The main purpose of this study is to look at whether meditation techniques can help reduce pain and opioid use after surgery.
- Conditions
- Arthropathy of Knee, Osteo Arthritis Knee, Osteonecrosis, Meditation
- Trial name
- NCT05669066
- Testing
- Mindful meditation
- Where
- United States
- Volunteers
- 29 people, healthy volunteers welcome
- Sponsor
- Beth Israel Deaconess Medical Center
THA
Fascia Iliaca Blocks for Total Hip Arthroplasty
The development of minimal-incision techniques for total hip arthroplasty (THA) with preservation of soft tissue is generally associated with reduction of postoperative pain and increased patient comfort.
- Trial name
- NCT03691337
- Testing
- Marcaine 0.25 % Injectable Solution, Sodium chloride
- Where
- Belgium
- Volunteers
- 75 people, healthy volunteers welcome
- Sponsor
- New York School of Regional Anesthesia
Arthroplasty, Replacement, Knee, Arthroplasty, Replacement, Hip
Sleep Patterns After Total Joint Replacement Surgery
The purpose of this study is to determine sleep patterns and sleep quality following total joint arthroplasty, in order to understand when patients should expect to return to baseline or improved sleep following total joint…
- Trial name
- NCT04896892
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Henry Ford Health System
Total Hip Arthroplasty
Fish Oil in Total Hip Replacement Randomized Clinical Trial
The purpose of this study is to determine if continuing fish oil supplementation leads to higher blood loss in patients undergoing total hip arthroplasty (THA).
- Trial name
- NCT04360239
- Testing
- Fish Oil
- Where
- United States
- Volunteers
- 8 people
- Sponsor
- Jeffrey L Stimac MD
Total Hip Arthroplasty, Functional Recovery
Comparison of Three Different Surgical Approaches on the Functional Outcome After Total Hip Arthroplasty
This study aimed to determine differences in functional recovery after total hip arthroplasty between a group of patients operated on using a direct lateral approach, an anterolateral minimally invasive approach, and a posterior…
- Trial name
- NCT06141928
- Testing
- Functional recovery analysis
- Where
- Croatia
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Clinic for Orthopedics Lovran
Arthroplasty, Replacement, Thromboembolism
Pradaxa (Dabigatran Etexilate 220 mg/q.d. in the General Population After Hip or Knee Replacement Surgery
An observational cohort study on safety and efficacy of the 220 mg dose Pradaxa to generate additional data in predefined sub populations of patients at increased risk of bleeding or VTE
- Trial name
- NCT00846807
- Where
- 112 sites in Austria, France and 7 more
- Volunteers
- 5,476 people
- Sponsor
- Boehringer Ingelheim
Total Hip Arthroplasty (THA)
Clinical Performance of XPEO-E Liner in SERF Dual-mobility Cups
XPEO-E liner is CE marked under MDD 93/42/CEE by equivalency with CI E liner. No pertaining data on XPEO-E liner is yet available.
- Trial name
- 2024-01-XPEO-E (NCT06917365)
- Where
- 5 sites in France
- Volunteers
- 500 people
- Sponsor
- Societe dEtude, de Recherche et de Fabrication
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