Clinical trials: Hip Replacement, Total
Total Hip Arthroplasty (THA)
Early Rehabilitation After Total Hip Arthroplasty
This study aims to investigate the effects of an early postoperative rehabilitation program combined with neuromuscular electrical stimulation (NMES) and telerehabilitation on functional recovery in patients undergoing total hip…
- Trial name
- NCT07550647
- Testing
- Early Postoperative Physiotherapy, Neuromuscular Electrical Stimulation (NMES), Telerehabilitation
- Where
- Turkey (Türkiye)
- Volunteers
- 52 people
- Sponsor
- Muğla Sıtkı Koçman University
Chronic Hip Pain
Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and Fixation of the Stryker Trident II Tritanium System
The study aims to describe bone apposition and fixation of the Trident and Trident II Tritatnium acetabular system in patients 1 year status post total hip replacement.
- Trial name
- NCT03469817
- Testing
- MRI
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Hospital for Special Surgery, New York
Osteoarthritis, Hip, Arthroplasty Complications
Incidence of 30 Day Return to Hospital Following Same Day Discharge Total Hip Arthroplasty
Amongst patients who are discharged home from hospital on the same day as their elective Primary Total Hip Arthroplasty, the Investigators seek to quantify the incidence of return to hospital within 30 days of surgery for…
- Conditions
- Osteoarthritis, Hip, Arthroplasty Complications, Complication of Surgical Procedure, Perioperative Complication
- Trial name
- NCT04120324
- Testing
- Eligible for Same Day Discharge, Primary Single Joint Total Hip Arthroplasty, Discharge Same Day
- Where
- Canada
- Volunteers
- 109 people
- Sponsor
- University of British Columbia
Total Hip Replacement Surgery
Pharmacokinetic Study of the Penetration of Ceftobiprole in the Bone
This study is being performed to measure the amount of the antibiotic ceftobiprole (study drug) found in the bone and blood after receiving one dose prior to your elective hip replacement surgery.
- Trial name
- NCT00771524
- Testing
- Ceftobiprole
- Volunteers
- 22 people
- Sponsor
- Basilea Pharmaceutica
Pain, Postoperative
Erector Spinae vs Fascia Iliaca Block in Hip Arthroplasty
The thoracic erector spinae plane (ESP) block was first described by Forero et al in September 2016. In their article, the authors presented the possibility of using this block as an option for the control of thoracic neuropathic…
- Trial name
- ESFIBHA (NCT03860324)
- Testing
- Single-shot erector spinae plane block, Single-shot fascia iliaca block
- Where
- Portugal
- Volunteers
- healthy volunteers welcome
- Sponsor
- Hospital Beatriz Ângelo
Hip Arthropathy, Hip Disease
Cardiac Index and General Anesthesia Without Opioid.
General anesthesia used to be based on the association of hypnotics and opioid drugs. But recent studies showed that opioids may be related to a many different complications, like respiratory distress, hyperalgesia.
- Trial name
- OFFLOW (NCT05446623)
- Testing
- Dexmedetomidine, Sufentanil
- Where
- France
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Centre Hospitalier de Montauban
Hip Arthropathy
A Randomized Controlled Trial for Patients Underwent Total Hip Arthroplasties Assisted by Surgical Navigation System
This is a randomized controlled, multicenter study. According to the inclusion criteria, volunteers were recruited from patients undergoing total hip arthroplasty.
- Trial name
- NCT04711720
- Testing
- "VTS" surgical navigation system
- Volunteers
- 124 people
- Sponsor
- Peking University Third Hospital
Postoperative Complications, Postoperative Pain
Suprainguinal Fascia Iliaca Block Versus PENG Block for Hip Arthroplasty Analgesia
In recent years, suprainguinal fascia iliaca block (SFIB) has emerged as a reliable analgesic option for primary total hip arthroplasty (THA).
- Conditions
- Postoperative Complications, Postoperative Pain, Weakness, Muscle, Motor Activity
- Trial name
- NCT04402450
- Testing
- Ultrasound-guided suprainguinal fascia iliaca nerve block, Ultrasound-guided pericapsular nerves group of the hip block
- Where
- Chile
- Volunteers
- 40 people
- Sponsor
- University of Chile
Osteoarthritis, Osteoarthritis (OA) of the Knee
Feasibility of Choose to Move Replacement Ready
Choose to Move (CTM) is a 3-month, choice-based health-promoting program for low active older adults being scaled-up across British Columbia (BC), Canada.
- Conditions
- Osteoarthritis, Osteoarthritis (OA) of the Knee, Osteoarthritis, Hip, Total Knee Arthroplasty; Total Hip Arthroplasty
- Trial name
- CTM-RR (NCT07069179)
- Testing
- Choose to Move Replacement Ready
- Where
- Canada
- Volunteers
- 60 people
- Sponsor
- University of British Columbia
Total Knee Arthroplasty (Postoperative Pain), Total Hip Arthroplasty (Postoperative Pain)
Effects of tDCS Combined With CBI on Postsurgical Pain
The purpose of this study is to determine whether a new medical technology can help reduce post-operative total knee or hip pain when combined with a Cognitive-Behavioral intervention (CBI).
- Trial name
- tDCS-CBI (NCT04199780)
- Testing
- Transcranial Direct Current Stimulation, Cognitive-Behavioral (CB) intervention
- Where
- United States
- Volunteers
- 106 people
- Sponsor
- VA Office of Research and Development
Total Hip Replacement
A Comparison of Large Diameter Metal Heads vs. Small Diameter Metal Heads vs/ Dual Mobility Total Hip Replacements
Does having a large diameter metal on polyethylene total hip replacement increase metal ion release. Larger metal heads are thought to have increased torsional forces on the trunion which would like release more metal ions.
- Trial name
- NCT02049892
- Testing
- Metal Ion Levels
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Mayo Clinic
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
Pain Management, Total Hip Arthroplasty
Ultrasound-Guided Quadro-Iliac Plane Block for Pain Management After Total Hip Arthroplasty
This prospective, randomized, double-blind study evaluates the analgesic effectiveness of the ultrasound-guided Quadro-Iliac Plane (QIP) block in patients undergoing primary total hip arthroplasty.
- Trial name
- NCT07410000
- Testing
- Quadro-Iliac Plane (QIP) Block
- Where
- Turkey (Türkiye)
- Volunteers
- 100 people
- Sponsor
- Bursa City Hospital
Arthritis
Fascial Manipulation® Associated With Standard Care Versus Standard Post-surgical Care for Total Hip Arthroplasty
Post-surgical physiotherapy programs following to total hip arthroplasty (THA) show important differences between types and numbers of treatment sessions.
- Trial name
- NCT02576028
- Testing
- Fascial Manipulation® (FM), standard active exercises
- Volunteers
- 51 people, healthy volunteers welcome
- Sponsor
- Azienda Ospedaliera Bolognini di Seriate Bergamo
Neuromuscular Blockade, Innate Inflammatory Response
Impact of Deep Neuromuscular Blockade During Total Hip Replacement Surgery on Postoperative Recovery and Immune Function
Monocenter randomized controlled trial to compare the effect of deep neuromuscular blockade (NMB) versus moderate NMB during total hip replacement surgery on postoperative quality of recovery and innate immune function.
- Conditions
- Neuromuscular Blockade, Innate Inflammatory Response, Quality of Life, Postoperative Complications
- Trial name
- HIPPO (NCT05562999)
- Testing
- Rocuronium Bromide
- Where
- Netherlands
- Volunteers
- 100 people
- Sponsor
- Radboud University Medical Center
Osteoarthritis
Preoperative Resistance Training in Patients Scheduled for Total Hip Arthroplasty
Purpose: The purpose of this study is to determine the effect of pre operative resistance training on subjects scheduled for total hip arthroplasty due to primary osteoarthritis.
- Trial name
- NCT01164111
- Testing
- Preoperative resistance training
- Where
- Denmark
- Volunteers
- 80 people
- Sponsor
- University of Southern Denmark
Muscular Atrophy
A Study of LY2495655 in Older Participants Undergoing Elective Total Hip Replacement
The primary objective of this study is to test the hypothesis that appendicular lean body mass (aLBM) will increase after 12 weeks of LY2495655 treatment versus placebo in older participants undergoing elective total hip…
- Trial name
- NCT01369511
- Testing
- LY2495655
- Where
- 45 sites in United States, Austria and 9 more
- Volunteers
- 400 people
- Sponsor
- Eli Lilly and Company
Infections Joint Prosthetic, Overweight or Obesity
Antibiotic Prophylaxis in High-Risk Arthroplasty Patients
To determine the effectiveness of a 7-day course of an oral, prophylactic antibiotic on the incidence of periprosthetic joint infection and wound complications following primary total hip and knee arthroplasty in a high-risk…
- Conditions
- Infections Joint Prosthetic, Overweight or Obesity, MSSA Colonization, MRSA
- Trial name
- NCT04297592
- Testing
- Cephalexin, Doxycycline, Cefadroxil
- Where
- 2 sites in United States
- Volunteers
- 4,618 people
- Sponsor
- Mayo Clinic
Hip and Knee Joint Osteoarthritis, Hip and Knee Joint Arthroplasty
Effectiveness of Exercise Programs Following Total Hip and Knee Joint Arthroplasty
The purpose of the study was to evaluate the effectiveness of balance exercises added to typical joint range of motion and muscle strengthening exercises on balance in patients following total hip or knee joint arthroplasty
- Trial name
- NCT01555307
- Testing
- Typical range of motion and muscle strengthening exercises, and balance exercises, Typical group
- Where
- Canada
- Volunteers
- 82 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Total Hip Arthroplasty
Efficacy of Intravenous Oxytocin to Speed Recovery After THA
The purpose of this study is to test whether perioperative intravenous (IV) oxytocin compared to placebo results in faster recovery in disability as measured by daily steps over 56 days after Total Hip Arthroplasty (THA).
- Trial name
- NCT07430228
- Testing
- intravenous administration of oxytocin
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Wake Forest University Health Sciences
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