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Forearm Fracture clinical trials

View clinical trials related to Forearm Fracture.

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NCT ID: NCT03297047 Completed - Radius Fractures Clinical Trials

Comparing Forearm and Upper Arm Combi Cast for Distal Forearm Fractures in Children

Start date: October 2, 2017
Phase: N/A
Study type: Interventional

The standard treatment for children with closed reduction of displaced distal forearm fractures is an immobilization with an upper arm combicast. The hypothesis is that an forearm immobilization with combicast in children 4-16 years might be sufficient.

NCT ID: NCT03097757 Terminated - Ultrasound Clinical Trials

Trial of Ultrasound Guidance for Reduction of Pediatric Forearm Fractures

Start date: January 24, 2017
Phase: N/A
Study type: Interventional

The primary objective of this study is to assess the utility of ultrasound guidance in the closed reduction of pediatric forearm fractures in the pediatric emergency department. The investigators will compare post-reduction radiologic outcomes between the experimental group (ultrasound guided closed forearm fracture reduction) and control group (standard of care blinded closed forearm fracture reduction) to determine if there is a difference in the number of adequate reductions between groups. Secondary objectives include comparing provider satisfaction with the reduction procedure, number of patients requiring repeat reductions, time for reduction, number of patients requiring operative repair after reduction, with the reduction procedure and comparison between post-reduction ultrasound and x-ray interpretation.

NCT ID: NCT02769117 Completed - Clavicle Fracture Clinical Trials

Bone Ultrasound to Access Fracture Healing

Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate sequential fracture healing with radius/ulna fractures or clavicle fractures and compare ultrasound to radiographs.

NCT ID: NCT01567072 Completed - Forearm Fracture Clinical Trials

Non Steroidal Antiinflammatory Drugs Influence on Heal of Distal Radius Fracture

CHIP
Start date: April 2012
Phase: Phase 3
Study type: Interventional

It is believed, that Non Steroidal Antiinflammatory Drug (NSAID) drugs slows bone healing, but the knowledge is based only on animal studies, and the results are automatically raised for the people. Many patients with bone fracture must therefore avoid the formerly so popular and good painkillers, although no clinical trial evidence is, that this medicine is really harmful for patients with fractures. The purpose of this study is to investigate whether these drugs slows bone healing, and what the relationship is between various bone studies - DEXA scanning, biochemical bone marker tests, radiographic controls and tissue examination of newly formed bone under a microscope. How sensitive and specific, each of the above study methods? If they are just as sensitive, the cheapest of them recommended as a routine investigation on suspicion of bone effects. Furthermore, to compare the benefit (pain-relieving effect, influence on rehabilitation) of these drugs and their possible harmful side effects (affected and delayed bone healing). The expectation is that the study may contribute to increased knowledge about NSAIDs effect do pain management, rehabilitation and the entire treatment process significantly easier and safer, so that patients recover faster and return to usual activities.

NCT ID: NCT00775554 Withdrawn - Forearm Fracture Clinical Trials

Comparison Study of Using Ultrasound Guidance for Hematoma Blocks vs. Traditional Approach

Start date: September 2008
Phase: N/A
Study type: Interventional

Will use visual analog scales to compare effectiveness of traditional hematoma block vs ultrasound guided hematoma block with regards to pain. This will be done for closed forearm fractures.

NCT ID: NCT00763880 Terminated - Forearm Fracture Clinical Trials

Hematoma Block as an Adjunct to Procedural Sedation for Forearm Fracture Reduction

Start date: November 2005
Phase: Phase 4
Study type: Interventional

The purpose of our study is to determine if the use of a hematoma block together with intravenous sedation and analgesia is an effective means of managing forearm fractures in the Emergency Department. To determine this, we have designed a randomized, double-blind, placebo controlled trial of hematoma block versus saline for the manipulation of forearm fractures under conscious sedation with ketamine and midazolam. Our hypotheses are two-fold: First, the use of a hematoma block together with conscious sedation will allow for improved pain control. Second, the use of a hematoma block together with conscious sedation will allow us to use less sedation, therefore promoting faster recovery from sedation and more efficient patient turnover in the Emergency Department.

NCT ID: NCT00239889 Completed - Forearm Fracture Clinical Trials

Efficacy and Safety of Salmon Calcitonin Nasal Spray in Improving Muscle Strength and Reducing Pain After Forearm Fracture in Postmenopausal Women

Start date: March 2002
Phase: Phase 4
Study type: Interventional

Calcitonin has been used for many years for treating osteoporosis in postmenopausal women, and it has been shown that calcitonin reduces pain after spine and hip fracture in women with osteoporosis. Therefore, this study assesses the safety and efficacy of salmon calcitonin nasal spray on muscle strength after a forearm fracture, pain, quality of life and fracture healing in postmenopausal women.