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Fractures, Bone clinical trials

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NCT ID: NCT02521415 Completed - Bone Fracture Clinical Trials

IN Sub-Dissociative Ketamine vs IN Fentanyl

Start date: December 2015
Phase: Phase 2
Study type: Interventional

This single center, randomized control, double blind trial will prospectively examine the feasibility of intranasal, sub-dissociative (IN) ketamine versus intranasal fentanyl for pain control in the pediatric emergency department setting. The investigators hypothesize that IN ketamine may provide a safe and effective alternative to IN fentanyl for children with suspected, isolated extremity fractures. Eighty children ages 3-17 years with a suspected, isolated extremity fracture that requires analgesia will be randomized to receive IN ketamine or IN fentanyl upon presentation to the emergency department and will be followed for 2 hours for efficacy and 6 hours for safety.

NCT ID: NCT02514993 Completed - Clinical trials for Thoracic Spine Fracture

The Unstable Thoracic Cage Injury

Start date: January 2003
Phase: N/A
Study type: Observational

- Analysis of patient data and computed tomography scan of polytraumatized patients thoracic spine fractures - A concomitant sternal fracture was identified an indicator for an unstable thoracic spine fracture

NCT ID: NCT02514343 Completed - Radius Fracture Clinical Trials

Magnesium Sulfate and Bupivacaine for Rehabilitation After Distal Radius Fractures

Start date: July 2015
Phase: N/A
Study type: Interventional

This study evaluates the effect of 10% magnesium sulfate in the rehabilitation of the wrist mobility in patients with distal radius fracture treated with percutaneous pinning and plaster

NCT ID: NCT02512094 Completed - Hip Fracture Clinical Trials

Validity and Reliability of Thai Version of Barthel Index for Hip Fracture Patients

Start date: June 2014
Phase: N/A
Study type: Observational

Since an increasing in population age, there was an increasing in geriatric patients. Most of elderly patients needed rehabilitation programs to regain their quality of life during their medical treatments. Barthel index is a functional measurement to evaluate rehabilitation improvement in chronically-ill patients and also used for evaluation of patient's self-care. Barthel index had been translated into many languages and validated in many medical conditions such as spinal cord injury, congestive heart failure, pneumonia, etc. However, Barthel index had not been translated into Thai language and validated to use in hip fracture patients. The purposes of this study were to translate the Barthel index into Thai language and to assess validity and reliability of Thai version Barthel index in hip fracture patients.

NCT ID: NCT02507505 Completed - Hip Fractures Clinical Trials

Regional Versus General Anesthesia for Promoting Independence After Hip Fracture

REGAIN
Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if two types of standard care anesthesia are the same or if one is better for people who have hip fractures.

NCT ID: NCT02507193 Completed - Clinical trials for Distal Fibula Fracture

Fibular Fixation in Ankle Fractures:Plate Verses Nail.

Start date: July 2015
Phase: N/A
Study type: Interventional

The primary objective of this study will be to evaluate the functional outcome of patients who present with a distal fibula fracture who were treated with either intermedullary nail (IMN) fixation or plate fixation.

NCT ID: NCT02498717 Completed - Ankle Fractures Clinical Trials

Preliminary Review of Cold and Active Compression Therapy for Traumatic Calcaneus or Ankle Fractures

Start date: June 3, 2015
Phase: N/A
Study type: Interventional

This study will examine the initial efficacy and cost-effectiveness of using the cryocompression therapy model both pre-operatively and post-operatively in patients that have recently suffered a traumatic calcaneus or ankle fracture compared to the standard pre-operative RICE therapy procedures.

NCT ID: NCT02495688 Completed - Postoperative Pain Clinical Trials

Regional or General Anesthesia for Distal Radius Fracture Surgery in a Day Surgery Setting

Start date: March 23, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare general and regional anesthesia with regard to postoperative pain in patients who undergo surgery in a day surgery setting due to a displaced distal radius fracture.

NCT ID: NCT02494011 Completed - Clinical trials for Distal Radius Fracture

Closed Kinetic Chain Exercise Versus Russian Current Stimulation in Rehabilitation of Colles' Fracture.

Start date: January 2014
Phase: N/A
Study type: Interventional

This study compared the effects of closed kinetic chain exercise and Russian current stimulation on pain, functional disability, wrist range of motion (ROM) and grip strength in patients with colles' fracture. Forty five patients with stable colles' fractures are randomly classified into three groups with fifteen patients in each group; Group I received traditional exercise in the form of; Mobilization, stretching exercises, range of motion exercises (passive and active) and edema control of the wrist joint. Group II stimulated by electrical Russian current in addition to traditional exercise. Group III received closed kinetic chain exercise (wall press, plyometric wall push up, Quadruped rhythmic stabilization, and Push up exercises) plus traditional exercise. All outcome measures including Pain, function, Wrist ROM, and grip strength were evaluated before and after the treatment program.

NCT ID: NCT02491047 Completed - Tibial Fractures Clinical Trials

Safety and Performance of BonyPid-1000™ in the Treatment of Gustilo I, II, IIIA and IIIB Tibial Open Fractures

Start date: October 2015
Phase: N/A
Study type: Interventional

This is a prospective, multi-national, multicenter, randomized, two arms, single blind, Standard of Care (SOC) controlled, with blinded central reading center study. This study will assess the safety and performance of BonyPid-1000™ in severe open tibial fractures (Gustilo IIIA and IIIB) when implanted as adjunct to SOC and compared to SOC alone.