Clinical trials: Fracture Bone
Proximal Humeral Fracture
Perioperative Complications in Reversed Shoulder Arthroplasties
Retrospective observational study of reversed shoulder arthroplasties by proximal humeral fracture. Analysis of preoperative risk factors as well as minor and major complications at the first week, 90 days and 1 year.
- Trial name
- NCT03243409
- Where
- Spain
- Volunteers
- 105 people
- Sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Hip Fracture
Peripheral Nerve Blocks in Elderly Patients With Hip Fracture
As the population ages, the frequency of surgery is increasing proportionally, bringing with it the challenge of managing older patients with frequent comorbid diseases and an increased risk of complications.
- Trial name
- NCT02635763
- Testing
- Femoral nerve and the lateral cutaneous nerve block, Lumbar plexus and sacral plexus nerve block
- Where
- China
- Volunteers
- 60 people
- Sponsor
- Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Fast-track Protocol, Hip Fracture
IMPLICATION OF FAST-TRACK PROTOCOL FOR HIP FRACTURE FIXATION IN ALEXANDRIA UNIVERSITY HOSPITALS
The present study aims to evaluate the impact of fast-track protocol of hip fracture fixation within 48 hours on patients' mortality and morbidities.
- Conditions
- Fast-track Protocol, Hip Fracture, 30 Days Mortality
- Trial name
- NCT06881121
- Testing
- Fast-track protocol for hip fracture fixation
- Where
- Egypt
- Volunteers
- 150 people
- Sponsor
- Alexandria University
Hip Fractures, Supra-inguinal Fascia Iliaca Block
Preoperative Supra-inguinal Fascia Iliaca Block for Positioning Analgesia in Hip Fracture Patients Undergoing Spinal Anesthesia
The goal of the clinical trial is to learn if preoperative Superficial Inguinal Fascia Iliaca (SIFI) block works to reduce pain during positioning for spinal anesthesia.
- Conditions
- Hip Fractures, Supra-inguinal Fascia Iliaca Block, Spinal Anesthesia
- Trial name
- NCT07556614
- Testing
- Isobaric bupivacaine 0.5%
- Where
- Pakistan
- Volunteers
- 132 people
- Sponsor
- Ghurki Trust and Teaching Hospital
Hip Fractures
The HIP Impact Protection Program (HIP PRO)
HIP PRO is a multicenter randomized, controlled trial of an energy absorbing and distributing padding system designed to reduce the incidence of hip fractures in 546 nursing home (NH) residents.
- Trial name
- NCT00058864
- Testing
- Energy absorbing and distributing trochanteric pad
- Where
- 4 sites in United States
- Volunteers
- 546 people, healthy volunteers welcome
- Sponsor
- National Institute on Aging (NIA)
Burst Fracture
Thoracolumbar Burst Fracture Treated With Pedicle Screws: Radiographic Outcomes
The surgical results of thoracolumbar and lumbar burst fracture have been reported to be comparable between patients with and without fusion in a midterm follow-up.
- Trial name
- NCT01979198
- Where
- Taiwan
- Volunteers
- 48 people
- Sponsor
- Taipei Veterans General Hospital, Taiwan
Ankle Fractures, Orthopedic Procedures
Outpatient Versus Inpatient Surgery for Ankle Fractures
This study is a single center randomized controlled trail in which we compare outpatient and inpatient patients with an ankle fracture requiring surgical treatment.
- Conditions
- Ankle Fractures, Orthopedic Procedures, Surgical Procedures, Inpatient
- Trial name
- OVISAF (NCT05389436)
- Testing
- Ambulatory care, Inpatient care
- Where
- Denmark
- Volunteers
- 86 people
- Sponsor
- Christian Grundtvig Refstrup Rasmussen
Spinal Fusion, Lumbar Fusion
Lumbar Fusion With Porous Versus Non-Porous Cages
The objective of this single site, randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo lumbar interbody fusion procedures (TLIF), supplemented with pedicle screw…
- Conditions
- Spinal Fusion, Lumbar Fusion, Arthrodesis, Spondylolisthesis
- Trial name
- NCT05583864
- Testing
- CONDUIT Porous Titanium Spinal Cage, PROTI 360 Titanium-Coated PEEK Spinal Cage
- Where
- United States
- Volunteers
- 108 people
- Sponsor
- Francis Farhadi
Distal Radius Fracture Reduction, Pain Control
Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures
The aim of this study is to evaluate the efficacy of a hematoma block and minimal ketamine pain control or hematoma block and intranasal fentanyl in pediatric patients presenting with distal radius fractures requiring reduction…
- Conditions
- Distal Radius Fracture Reduction, Pain Control, Pediatric Fractures
- Trial name
- NCT07120763
- Testing
- Ketamine + Lidocaine, Ketamine group, Fentanyl (Nasalfent, Fentanyl Citrate Nasal Spray)
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- State University of New York at Buffalo
Urinary Incontinence, Postpartum
Efficacy of Physiotherapy for Urinary Incontinence in Women With a Puborectalis Avulsion
Childbirth is a major risk factor for pelvic floor muscle (PFM) trauma. In one third of women, stretching of the PFM will result in an avulsion injury (i.e.
- Conditions
- Urinary Incontinence, Postpartum, Pelvic Floor; Perineal Rupture, Obstetric, Physiotherapy
- Trial name
- NCT03254355
- Testing
- Multimodal physiotherapy
- Where
- Canada
- Volunteers
- 126 people
- Sponsor
- Université de Sherbrooke
Mandibular Fractures
Validity of Computed Guided Technology in Proper Placement of Intermaxillary Fixation Screws in Mandibular Fractures
A randomized clinical study that aims to assess the validity of the use of computer guided technique in the proper placement of IMF screws in mandibular fractures
- Trial name
- NCT06883331
- Testing
- intermaxillary fixation using IMF screws, intermaxillary fixation using IMF screws with surgical guide
- Where
- Egypt
- Volunteers
- 20 people
- Sponsor
- Suez Canal University
Pseudoarthrosis of Bone, Pseudarthrosis
Treatment of Nonunion Fractures With Mesenchymal Stromal Cells (MSCs)
The goal of this study is to evaluate the bone regeneration capacity of BM-MSC (Bone marrow mesenchymal stromal cells), in patients with nonunion.
- Conditions
- Pseudoarthrosis of Bone, Pseudarthrosis, Non Union Fracture, Nonunion Bone Fracture
- Trial name
- MSC (NCT06103396)
- Testing
- Transplantation of autologous MSCs in nonunion fracture, Transplantation of allogeneic MSCs in nonunion fracture
- Where
- Venezuela
- Volunteers
- 30 people
- Sponsor
- Instituto Venezolano de Investigaciones Cientificas
Proximal Humeral Fractures
Effect of Osteosynthesis, Primary Hemi-arthroplasty, and Non-surgical Management for Fractures of the Proximal Humerus
Displaced four-part fractures are among the most severe injuries of the proximal humerus. The optimal treatment is disputed and published data are inadequate for evidence-based decision making.
- Trial name
- NCT00835562
- Testing
- Non-surgical management, Osteosynthesis, Hemiarthroplasty
- Where
- Denmark
- Volunteers
- 162 people
- Sponsor
- Herlev Hospital
Fractures, Bone, Fracture Complications
Comparison of the Safety and Cost of a Simplified Post-Operative Radiograph (SPOR) Protocol
The standard post-operative radiographic protocol for the monitoring of fractures at Health Sciences Centre includes post-operative in hospital radiographs as well as radiographs at the two week follow up appointment.
- Conditions
- Fractures, Bone, Fracture Complications, Xray Complication
- Trial name
- SPOR (NCT04110470)
- Testing
- X-ray, No-Xray
- Volunteers
- 1,612 people
- Sponsor
- University of Manitoba
Rheumatoid Arthritis, Osteoarthritis
A Study to Assess the Long-term Performance of SmartSet® HV and SmartSet® GHV Bone Cements in Primary Total Hip Replacement
The purpose of this study is to monitor the performance of artificial hip joints implanted with two different bone cements, SmartSet® HV and SmartSet® GHV, in the treatment of patients with hip joint disease requiring a total hip…
- Conditions
- Rheumatoid Arthritis, Osteoarthritis, Post-traumatic Arthritis, Collagen Disorders
- Trial name
- NCT00872066
- Testing
- SmartSet® HV bone cement, SmartSet® GHV bone cement
- Where
- Slovakia
- Volunteers
- 243 people
- Sponsor
- DePuy International
Hip Injuries, Hip Dislocation
Does Limb Pre-Conditioning Reduce Pain After Hip Arthroscopy
The purpose of this study is to determine if the utilization of Ischemic Pre-Conditioning 24-hours prior to hip arthroscopy decreases patient's post-operative pain and opioid consumption.
- Conditions
- Hip Injuries, Hip Dislocation, Hip Fractures
- Trial name
- NCT04925791
- Testing
- standardized pre-conditioning treatment, Partial occlusion
- Where
- United States
- Volunteers
- 68 people, healthy volunteers welcome
- Sponsor
- Cedars-Sinai Medical Center
Pes Planus
The Development of Flat Foot After Ankle Fractures
In this study we are trying to determine the incidence of flat foot (also called pes planus) among patients who have had an ankle fracture.
- Trial name
- NCT00507910
- Where
- Canada
- Volunteers
- 25 people
- Sponsor
- Ottawa Hospital Research Institute
Fracture
Subcapital and Shaft Fractures of the 5. Metacarpal
The purpose of this study is to find out the best treatment for subcapital and shaft fractures of the 5. metacarpal. It is a prospective randomized multicenter study. Comparing only fractures dislocated more than 30 degrees.
- Trial name
- NCT01242982
- Testing
- Closed reduction and fixation with 2 pins, Reduction and Plaster of Paris
- Where
- 5 sites in Norway
- Volunteers
- 39 people, healthy volunteers welcome
- Sponsor
- St. Olavs Hospital
Hip Fractures
Comparison of Pericapsular Nerve Group Block With Suprainguinal Fascia Compartment Block in Hip Fractures
Ultrasound-guided Supra-inguinal Fascia Iliaca compartment Block (SIFCB) and Pericapsular Nerve Group Block (PENG) are increasingly being used for postoperative analgesia for hip surgery.
- Trial name
- NCT06169462
- Testing
- PENG block, PENG block+ SIFCB
- Where
- Turkey (Türkiye)
- Volunteers
- 38 people, healthy volunteers welcome
- Sponsor
- Karaman Training and Research Hospital
Tibial Plateau Fractures
Genicular Nerve Block After Open Reduction Internal Fixation of Tibial Plateau
The investigators are conducting this research study to find better ways of treating pain following knee surgery. There is a standard (accepted) approach, which involves injection of numbing medication into the area around the…
- Trial name
- NCT06639503
- Testing
- Bupivacain
- Where
- United States
- Volunteers
- 38 people
- Sponsor
- University of Chicago