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Femoral Shaft Fracture clinical trials

View clinical trials related to Femoral Shaft Fracture.

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NCT ID: NCT06160804 Not yet recruiting - Clinical trials for Femoral Shaft Fracture

Evaluating Femoral Traction

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

The primary goal of this study is to test the hypothesis that skeletal traction allows for easier intraoperative reduction time by comparing the reduction time in patients that receive skeletal traction for femoral shaft fracture to those that do not. Secondary goals are to assess the claims of improved pain control and decreased blood loss in patients that receive skeletal traction for femoral shaft fracture to those that do not.

NCT ID: NCT06078371 Not yet recruiting - Clinical trials for Femoral Neck Fractures

Opioid-Free Pain Treatment in Trauma Patients

Start date: October 2023
Phase: N/A
Study type: Interventional

Analgesic drug study that will compare pain outcomes of opioid analgesia and opioid-free analgesia in post-operative orthopedic patients.

NCT ID: NCT05627479 Not yet recruiting - Clinical trials for Femoral Shaft Fracture

MAGIK for Femoral/Tibial Shaft Fractures

MAGIK
Start date: December 1, 2024
Phase: Phase 2
Study type: Interventional

The purpose of this phase 2 randomized control trial will be to evaluate the effect of glucose-insulin-potassium (GIK) therapy in the setting of lower extremity trauma to reduce short- and long-term muscle damage, acute rhabdomyolysis, and acute kidney injury. The study will consist of 40 patients with femur or tibial shaft fractures randomized to the GIK arm (using a well-described systemic GIK protocol; n = 20) or the control arm (using isotonic saline; n = 20). The use of systemic GIK is expected to decrease the overall amount of lower extremity muscle cell death and result in improved muscle function in the postoperative period. Additionally, the investigators hypothesize that GIK will lead to less severe rhabdomyolysis and a concomitant decrease in the incidence of AKI that results from the byproducts of muscle cell death.

NCT ID: NCT05362864 Recruiting - Osteotomy Clinical Trials

ZNN Bactiguard Cephalomedullary Nails PMCF Study

Start date: January 23, 2023
Phase:
Study type: Observational

This is a multicenter, prospective, Post-market Clinical Follow-up (PMCF) Study on the ZNN Bactiguard Cephalomedullary Nails. The objective of this study is to collect data confirming the safety, performance, and clinical benefit of the study device and instrumentation when used for the temporary internal fixation and stabilization of trochanteric, sub-trochanteric or shaft femoral fractures and osteotomies. This is a CE-marked device already available on the market and the aim of the study is to comply with the post-market surveillance requirements.

NCT ID: NCT04803591 Withdrawn - Clinical trials for Femoral Shaft Fracture

This is a Study to Verify if Tranexamic Acid Can Reduce the Anemia After a Femoral Shaft Fractures Surgery

ORL-ORT-023
Start date: August 1, 2021
Phase: Phase 4
Study type: Interventional

The investigators are going to evaluate if adding Tranexamic Acid in femoral shaft fractures surgery can lead to any advantages to the participants, namely if it can reduce post-operative anaemia, blood loss, blood transfusion requirements, length and cost of hospitalisation.

NCT ID: NCT04311866 Withdrawn - Pediatric ALL Clinical Trials

Femoral Pediatric Fractures. Walking Spica Cast vs Synthetic Pants

Start date: January 4, 2020
Phase: N/A
Study type: Interventional

Femoral pediatric shaft fractures are a common orthopedic injury. Conservative treatment is still the preferred method by orthopedic surgeons. The walking spica cast is used in patients between 1 year old and 6 years old, in patients with isolated and low-energy fractures. The use of synthetic materials is preferred (fiber glass) for resistance, durability and low weight makes them optimal.

NCT ID: NCT04195334 Not yet recruiting - Clinical trials for Femoral Shaft Fracture

IMN Diameter to Femoral Canal Diameter and Union

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

To Detect the Relation Between the Intramedullary Nail Diameter to Canal Ratio and the Incidence of Non-union

NCT ID: NCT03794622 Recruiting - Clinical trials for Femoral Shaft Fracture

Autologous Bone Marrow Concentration for Femoral Shaft Fracture Union

Start date: June 14, 2017
Phase:
Study type: Observational

This study aims to evaluate the effect of bone marrow concentration on union of femoral shaft fracture by comparing clinical and imaging outcomes between patients receiving Intramedullary nail fixation with intraoperative bone marrow concentration and those receiving Intramedullary nail fixation only.

NCT ID: NCT03251534 Completed - Clinical trials for Femoral Shaft Fracture

Contribution of Stereography (EOS Imaging System) in the Quantification of Femoral Shaft Fractures.

FEOS
Start date: September 2015
Phase:
Study type: Observational

This observational study is a collection of clinical and imaging data of patients with a femoral shaft fracture treated by nails. The aim of this research is the contribution of the EOS imaging system in the quantification of malunions.

NCT ID: NCT03211546 Active, not recruiting - Clinical trials for Femoral Shaft Fracture

Pediatric Femur Fracture Registry

PedFemFx
Start date: March 14, 2018
Phase:
Study type: Observational [Patient Registry]

Prospective data collection and evaluation of complete data sets will be performed in the course of routine clinical care of a cohort of consecutive patients (children up to 16 years old) presenting with an isolated femur shaft fracture. Data will be collected during follow-up visits at 3 to 6 weeks, 3, 6, 12 and 24 months, with additional follow-up visits as needed or dictated by individual practice. Final follow-up will be at 24 months, unless a patient requires additional follow-up or another intervention to address an unfavorable outcome (e.g. malalignment, nonunion, limb length discrepancy) noted at the 24 month follow-up visit.