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Fractures, Bone clinical trials

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NCT ID: NCT05225753 Completed - Femur Fracture Clinical Trials

Post-operative Anemia in Lateral Fractures of the Femur.

Start date: November 1, 2020
Phase:
Study type: Observational

It was conducted a prospective study with a series of 45 patients with lateral fragility fractures of the femur treated by three different intramedullary nails. Patients were randomized in Group A (15 patients treated by Affixus Zimmer-Biomet), Group B (15 patients treated by EBA2 - Citieffe) and Group C (15 patients treated by Proximal Femoral Nail Antirotation Synthes). One independent observer performed seven biochemical evaluations (hemoglobin serum value) from admission to patient discharge. Surgical time and Blood transfusions number were reported for each partecipant.

NCT ID: NCT05215626 Active, not recruiting - Clinical trials for Pelvic Ring Fracture

PMCF Study on the Safety, Performance and Clinical Benefits Data of the Zimmer® Reconstruction System

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

The study is a monocentric, retrospective, non-randomized, non-controlled and consecutive series post-market study. The purpose of this study is to confirm safety, performance and clinical benefits of the Reconstruction System (implants and instrumentation) when used for temporary internal fixation and stabilization of fractures during the normal healing process. The primary objective is the assessment of performance by analyzing fracture healing. The secondary objectives are the assessment of safety by recording and analyzing the incidence and frequency of complications and adverse events. Relation of the events to implant, instrumentation and/or procedure should be specified. Subjects' outcomes will also be assessed.

NCT ID: NCT05215613 Completed - Clinical trials for Proximal Humeral Fracture

PMCF Study on the Safety, Performance and Clinical Benefits Data of the Zimmer® Plates and Screws System

Start date: March 15, 2023
Phase:
Study type: Observational

The study is a monocentric, retro- and prospective, non-randomized, non-controlled and consecutive series post-market study. The purpose of this study is to confirm safety, performance and clinical benefits of the Zimmer® Plates and Screws System (implants and instrumentation) when used to stabilize diaphyseal, proximal humerus and proximal tibia fractures. The primary objective is the assessment of performance by analyzing fracture healing. The secondary objectives are the assessment of safety by recording and analyzing the incidence and frequency of complications and adverse events. Relation of the events to implant, instrumentation and/or procedure should be specified. Subjects' outcomes will also be assessed.

NCT ID: NCT05215236 Enrolling by invitation - Clinical trials for Distal Radius Fracture

Opiate Sparing Protocol Randomized Controlled Trial in Open Distal Radius Fracture Repair

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

A comparison of oral morphine equivalents between an opiate sparing cohort and an opiate based cohort following open reduction internal fixation of a distal radius fracture.

NCT ID: NCT05206981 Recruiting - Traumatic Fracture Clinical Trials

Device Global Registry for the IlluminOss Bone Stabilization System

Start date: June 11, 2021
Phase:
Study type: Observational [Patient Registry]

This is a multi-center, observational patient registry. The primary objective of the study is to collect safety and performance data on the IlluminOss Device when used to provide stabilization and alignment for the treatment of traumatic or impending and pathologic fractures.

NCT ID: NCT05197335 Active, not recruiting - Hip Fractures Clinical Trials

Observational Clinical Study on Elderly Patients With Fracture of the Proximal Femur Treated With the Chimaera Nail

Chimaera
Start date: July 9, 2020
Phase:
Study type: Observational

This is an observational, prospective and multicenter clinical investigation that is part of the active materiovigilance plan that Orthofix Srl, in agreement with its Notified Body. The sponsor has planned to actively collect clinical data relating to the use of Chimaera Intramedullary Nail in a representative number of users and elderly patients with fractures of the proximal femur. The data obtained from this clinical investigation will be used to complete the pre-market clinical evaluation carried out on the Chimaera with post-market clinical data from the use of the device in normal clinical practice.

NCT ID: NCT05193695 Terminated - Rehabilitation Clinical Trials

How to Reduce Dry Needling Pain in Treatment of Trigger Points of Muscle Triceps Sural in Ankle Post Fracture Patients

Start date: August 9, 2018
Phase: N/A
Study type: Interventional

Ankle fractures are one of the main causes of hospitalization due to injuries in Chile, which also have a discharge and partial load time of approximately 12 weeks in the recovery process. This generates disuse and atrophy of the posterior musculature of the leg called the triceps sural, which makes it difficult to restart and perform the gait. We conducted this research because practically all patients with this type of diagnosis have trigger points in these muscles, and dry needling technique is one of the best for its treatment, but has the disadvantage that it produces post dry needling pain of 48 hours and there is not enough information, or consensus on which method is better to reduce post dry needling pain. This study aims to prove wich technique is most useful in reducing pain post dry needling for the treatment of trigger points in the triceps sural muscle in ankle post fracture patients.

NCT ID: NCT05187585 Recruiting - Fractures, Bone Clinical Trials

Assessment of the Contribution of an Artificial Intelligence Tool to Help the Diagnosis of Limb Fractures in Pediatric Emergencies

FRACPED
Start date: February 10, 2022
Phase: N/A
Study type: Interventional

Limb fracture is a common pathology in children. It represents the first complaint in traumatology among children in developed countries. Failure to diagnose a fracture can have severe consequences in pediatric patients with growing bones, that can lead to delayed treatment, pain and poor functional recovery. X-ray is the first tool used by doctors to diagnose a fracture. However, the diagnosis of fracture in the emergency room can be challenging. Most images are interpreted and processed by emergency pediatricians before being reviewed by radiologists (most often the day after). Previous studies have reported the rate of misdiagnosis in fracture by emergency physicians from 5% to 15%. A tool to investigate in diagnosing limb fractures could be helpful for any emergency physicians exposed to this condition

NCT ID: NCT05186194 Recruiting - Vitamin d Clinical Trials

The Effect of Vitamin D and Calcium Supplementation on the Prevention of Stress Fractures.

Start date: September 30, 2021
Phase: N/A
Study type: Interventional

The main objective of this study is to find whether supplemental vitamin d and calcium can reduce the incidence of stress fractures in recruits. These high-risk recruits undergo intensive training which elevated bone turnover, which requires adequate level of vitamin D and calcium in order to support bone health. It is hypothesized that supplemental vitamin d and calcium will decrease the occurrence of stress fractures.

NCT ID: NCT05183477 Recruiting - Wrist Fracture Clinical Trials

Fast Track for Wrist and Scaphoid Fractures

Start date: December 17, 2021
Phase: N/A
Study type: Interventional

This is a mono centric, prospective, randomised trial on the implementation and assessment of a shortened pathway for mono-trauma of the wrist and suspected fracture of distal radius and/or ulna and/or scaphoid bone.