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Elbow Fracture clinical trials

View clinical trials related to Elbow Fracture.

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NCT ID: NCT02878941 Completed - Elbow Fracture Clinical Trials

Synovial Fluid Analysis of Intraarticular Elbow Fracture

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to obtain and compare bilateral elbow joint synovial fluid from patients with unilateral intraarticular elbow fracture and a contralateral healthy appearing elbow joint. The synovial fluid samples will undergo several forms of analysis for metabolites and proteins. Matched-pair statistical analysis will be performed to determine the metabolites and proteins that may play the greatest role in development of joint contracture.

NCT ID: NCT01944085 Completed - Elbow Fracture Clinical Trials

Percutaneous Pin Removal in Children - is Analgesia Necessary?

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

This is a simple randomised clinical trial to study if non-narcotic analgesia reduces the pain score and pulse rate of children who undergo removal of percutaneous pins in the outpatient clinic. Inclusion criteria: - 5-12 years of age - 2 or 3 percutaneous pins in either elbow Exclusion criteria: - documented or suspected allergies to acetaminophen, ibuprofen Patients enrolled in the study are instructed not take additional analgesia prior to the clinic visit (risk of overdosage explained). This is verified by clinic nurses conducting the trial. At the clinic visit, they are randomized into one of three groups 1. acetaminophen; 2. ibuprofen; or 3. Vitamin C (Placebo). They are served the `medication' (weight-appropriate dose) and the pins are removed in the clinic an hour later. Pain score (Wong-Baker scale) and pulse rate are measured before pin removal, immediately following pin removal, and 10 minutes after pin removal. The study hypothesis is that non-narcotic analgesia (such as acetaminophen and ibuprofen) do not decrease pain score and pulse rate associated with the pin removal procedure.

NCT ID: NCT01328782 Completed - Elbow Fracture Clinical Trials

The Post-Operative Pain Management of Pediatric Supracondylar Elbow Fractures

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

The goal of this study is to compare different ways of treating pain after surgery. This research study involves subjects who have a supracondylar elbow fracture and need surgery. This type of fracture occurs when the humerus (upper arm bone) is broken just above the elbow. Like any other surgery, you can expect that you will feel pain in the hours or days after the operation. Currently, despite the common occurrence of this surgery, there is not a standard way to treat and or prevent any of the pain afterwards. At this hospital, oral (take by mouth) pain medicine is commonly used to treat pain after this surgery. In this study, pain will be treated in one of the following ways: 1. with oral pain medication 2. with oral pain medicine and an intraarticular shot (a shot into the elbow joint) of bupivacaine (a "numbing" drug) or 3. with oral pain medicine and an intraarticular shot of ropivacaine (another "numbing" drug). The shots will be given during surgery. Your participation will help us find out which of these three pain control methods works the best. The correct dosages of all drugs will be safely prescribed by the doctor on an individual basis and all drugs will be used under the careful watch of your attending physician. All the drugs used this study are approved by the FDA for use in adults but they are not specifically approved for use in children. However, nearly 7 out of every 10 drugs approved for adults are not specifically approved by the FDA for use in children. All drugs used in this study will be used in a way that is considered to be safe and reasonable by the Children's Hospital.

NCT ID: NCT00991887 Terminated - Elbow Fracture Clinical Trials

Radiation Therapy for Heterotopic Ossification Prophylaxis Acutely After Elbow Trauma

ElbowHO
Start date: September 2005
Phase: N/A
Study type: Interventional

The investigators hypothesized that radiation therapy could be safely administered acutely after elbow trauma, and it would decrease the number of patients that would require surgical excision of heterotopic ossification.

NCT ID: NCT00580866 Terminated - Elbow Fracture Clinical Trials

Progressive Splinting Status Post Elbow Fractures and Dislocations

JAS
Start date: September 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to help determine if a static stretching brace in addition to physical therapy decreases the incidence of secondary operations, increases range of motion, and individual patient function.

NCT ID: NCT00521846 Active, not recruiting - Elbow Fracture Clinical Trials

ExploRâ„¢ Modular Radial Head Data Collection

Start date: August 2007
Phase:
Study type: Observational

The purpose of this prospective clinical data collection is to document the performance and clinical outcomes of the ExploR Modular Radial Head.