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Fractures, Bone clinical trials

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NCT ID: NCT05444803 Completed - Analgesia Clinical Trials

Femoral Nerve Block vs Peri-capsular Nerve Group Block for Hip Fracture Analgesia

Start date: July 6, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to compare the analgesic efficacy of femoral nerve block and peri-capsular nerve group block administered before spinal anesthesia for positioning to spinal anaesthesia in patients undergoing surgery for hip fracture and to evaluate the efficacy for postoperative analgesia

NCT ID: NCT05439512 Completed - Orbital Fractures Clinical Trials

Orbital Floor Fracture Repair by Titanium Mesh Via Transantral Approach.

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the feasibility of CAD/CAM osteosynthesis mesh through a transantral surgical approach in the Repair of orbital floor fractures by means of clinical and radiographic findings.

NCT ID: NCT05438784 Recruiting - Zygomatic Fractures Clinical Trials

Application of CAD-CAM Technology in Orbital Bone Reconstruction

CAD-CAM
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Reconstruction of orbital defects resulting after trauma; tumor resection; maxillary cyst; craniofacial anomalies and sequestrated boneā€¦. etc., has been a challenging issue over the years and this owing to the complicated anatomy of orbit. Inaccurate orbital reconstruction may lead to devastating cosmetic and functional complications. Titanium mesh for orbital reconstruction has now become "probably" the most popular material for orbital wall reconstruction worldwide. Innovation of CAD-CAM technology and its application in maxillofacial surgery will markedly improve the surgical outcome. This study will assess the accuracy of orbital reconstruction using CAD-CAM technology and to compare two different modalities for orbital reconstruction based on this technology.

NCT ID: NCT05437822 Recruiting - Clinical trials for Proximal Humeral Fracture

Tranexamic Acid in Proximal Humeral Fractures

Start date: June 29, 2022
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of tranexamic acid (on blood loss and transfusion requirements in patients with proximal humeral fractures requiring open surgical approaches. This a blinded, controlled, therapeutic trial in which the patients will be randomized to receive TXA or no drug intervention. The primary outcome is the estimated total blood loss. This study presents only minimal risks for the included patients.

NCT ID: NCT05435534 Recruiting - Osteoporosis Clinical Trials

Effect of a Multicomponent Intervention on Functional Capacity After Hip Fracture

ActiveFLS
Start date: May 26, 2022
Phase: N/A
Study type: Interventional

Due to the clinical, functional, cognitive and social complexity of older adults after fragility hip fractures (defined as those produced by low-impact trauma), the investigators propose an intervention. This intervention involves a multidisciplinary and multicomponent program consisting of physical exercise with tele-rehabilitation, nutritional assessment and other variables related to comprehensive geriatric assessment. The investigators want to improve functional status, quality of life and prevent new fractures. In addition, the investigators try to optimize treatments and resources based on the functional status of patients and their life expectancies, improving care and healthcare cost

NCT ID: NCT05435261 Not yet recruiting - Fractures, Open Clinical Trials

Ganga Hospital Scoring System In Type-IIIA/B Open Tibial Fractures

Start date: December 1, 2022
Phase:
Study type: Observational

The aim of this study is to assess interobserver reliability, sensitivity for amputation, and specificity for salvage of GHS in type-III injuries with open tibial fractures and predict the potential number of inpatient days, secondary procedures that would be required, and the rate of infection

NCT ID: NCT05430074 Completed - Clinical trials for Pediatric Supracondylar Humeral Fracture

HM vs Fibreglass Casts in Treating Pediatric Supracondylar Humeral Fractures

Start date: August 16, 2022
Phase: N/A
Study type: Interventional

Supracondylar humeral fractures are the most common elbow fractures in children and cast immobilization continues to remain as the recommended treatment for modified Gartland's classification Type I and Type IIa injuries. Apart from plaster of Paris and fibreglass casts, the use of waterproof, tubular hybrid mesh (HM) casts have been gaining traction for cast immobilization. Although the use of HM cast has been reported to have similar clinical outcomes and overall patient satisfaction scores to the fibreglass cast, the results of the recent studies are only limited and generalizable only to paediatric distal radius fractures. As the application method of HM and fibreglass casts are fundamentally different, it has not been reported if the difference in application duration between the cast materials is significant and its potential implications in outpatient clinic operation. Hence, through a randomized controlled trial, this study primarily aims to investigate if the clinical outcomes, patient satisfaction and duration of cast application with the HM casts would be comparable with fibreglass casts in children with supracondylar humeral fractures. Through this study, the investigators hope to evaluate the advantages and disadvantages of the respective casting material which may better aid physicians in deciding a more appropriate cast material for treating paediatric supracondylar humeral fractures with cast immobilization and the implications of casting duration on clinic operations.

NCT ID: NCT05429749 Recruiting - Hip Fractures Clinical Trials

Intravenous Iron Supplement to Prevent Postoperative Delirium After Hip Fracture Surgery

Start date: July 30, 2020
Phase: Phase 4
Study type: Interventional

This is a clinical trial to evaluate the effect of intravenous iron supplement with Ferinject (Ferric Carboxymaltose) in preventing postoperative delirium after hip fracture surgery.

NCT ID: NCT05426356 Active, not recruiting - Osteoporosis Clinical Trials

Sacral Fracture Fusion/Fixation for Rapid Rehabilitation

SAFFRON
Start date: September 18, 2022
Phase: N/A
Study type: Interventional

To determine the safety and efficacy of concomitant sacral fracture fixation and sacroiliac (SI) joint fusion vs. non-surgical management for patients with debilitating sacral fragility or insufficiency fractures

NCT ID: NCT05425758 Not yet recruiting - Clinical trials for Pediatric Distal Forearm Fractures

Optimal Index for Pediatric Distal Forearm Fractures

Start date: July 1, 2022
Phase:
Study type: Observational

This is a prospective radiographic study of displaced distal forearm fractures requiring manipulation for children 3-12 years of age and will be treated with casting.The patients' full radiographic series (including the pre-manipulation, immediate post-manipulation, after 1 week and after 4 weeks radiographs) will be evaluated.