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Fractures, Bone clinical trials

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NCT ID: NCT00586170 Terminated - Clinical trials for Nonunion of Fracture of Fifth Metatarsal

A Double-Blind Study on Adjunctive Use of PEMF in the Treatment of 5th Metatarsal Non-Union Fractures

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to analyze the effect of PEMF in surgical reconstruction of 5th metatarsal non-union fractures.

NCT ID: NCT00582998 Completed - Clinical trials for Fracture of Calcaneus, Pilon or Tibial Plateau

Vacuum Assisted Closure as a Treatment for Soft Tissue Injuries

VAC-ST
Start date: June 2001
Phase: N/A
Study type: Interventional

This project is designed as a prospective, randomized, comparative study evaluating the use of a negative pressure vacuum device in treating soft tissue injuries and the surgical incision following open reduction and internal fixation of calcaneus, tibial plateau, and pilon fractures.

NCT ID: NCT00582686 Completed - Calcaneus Fractures Clinical Trials

Open Reduction Internal Fixation of Calcaneus Fractures With and Without Bone Graft

CALCANEUS
Start date: May 2000
Phase: N/A
Study type: Interventional

The purpose of this study is to compare patient functional outcomes for surgical fixation of calcaneus fractures with and without tricortical iliac crest bone grafting

NCT ID: NCT00582439 Completed - Clinical trials for Orthopaedic Trauma Fractures and Non-unions

The Use of RIA to Harvest Bone Graft for Treatment of Non-unions and Fractures

RIA
Start date: January 2007
Phase: N/A
Study type: Interventional

This study is to determine the composition of bone graft harvested using the RIA system in 16 orthopaedic trauma patients between age 19 and 65 who have sustained a fracture or non-union requiring bone grafting. The patients will be followed to assess clinical outcomes and associated pain.

NCT ID: NCT00582361 Completed - Clinical trials for Orthopaedic Traumatic Open Fractures

Vacuum Assisted Closure as a Treatment for Open Fractures

VAC-OF
Start date: June 2001
Phase: N/A
Study type: Interventional

This project is designed as a prospective, randomized, comparative study evaluating the use of a negative pressure vacuum device in treating traumatic wounds sustained associated with an open fracture.

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: NCT00578019 Completed - Clinical trials for Supracondylar Femur Fracture

Comparison Between LISS Plating and Intramedullary (IM) Nailing for Supracondylar Femur Fractures

LISS
Start date: December 1999
Phase: N/A
Study type: Interventional

The purpose of this study is to compare patient outcomes for the Less Invasive Stabilization System (LISS) (Synthes {USA}, Paoli, PA, USA), a minimally invasive plating system used in the treatment of supracondylar femur fractures, with patient outcomes for the Supracondylar Nail (Smith & Nephew Inc, Memphis, TN, USA), a retrograde intramedullary nail.

NCT ID: NCT00560443 Completed - Pain Clinical Trials

RCT on Ketorolac and Tramadol in Bone Fractures Pain of Child

Start date: February 2008
Phase: Phase 4
Study type: Interventional

Randomized double blind Trial with the aim to estimate effectiveness of two therapeutic regimes per os on pain due to not compound bone fractures in child 4-17 years old: - ketorolac 0,5 mg/kg (1 drop every 2 Kg) - tramadol 2,5 mg/Kh (1 drop every 2 Kg) Intensity of pain will be estimated with linear 1 to 10 or analogic McGrath type scale every 20 min. The main objectives are the evaluation of pain decreasing in every group, the time of decreasing, the intensity of pain during procedures (ex. Xray) and the occurrence of side effects Secondary outcomes are comparison between the two groups on effectiveness on pain and on side effects

NCT ID: NCT00556842 Completed - Hip Fractures Clinical Trials

Comparing Total Hip Arthroplasty and Hemi-Arthroplasty on Secondary Procedures and Quality of Life in Adults With Displaced Hip Fractures

HEALTH
Start date: March 2009
Phase: N/A
Study type: Interventional

Each year, hip fracture, an injury that can impair independence and quality of life, occurs in about 280,000 Americans and 36,000 Canadians. By the year 2040, the annual healthcare costs associated with hip fractures are expected to reach $9.8 billion in the United States and $650 million in Canada. It is important to have in place optimal practice guidelines for the surgical handling of this injury. One type of hip fracture, called a displaced femoral neck fracture, is often treated with a hip replacement surgery. Patients undergoing a hip replacement may receive either a total hip replacement, in which the head of the femur and the hip joint socket are replaced, or a partial hip replacement, in which only the head of the femur is replaced. This study will compare the two different hip replacement procedures to determine which one results in better outcomes after surgery in adults aged 50 and older.

NCT ID: NCT00556543 Completed - Rib Fracture Clinical Trials

Clinical Study of the U-Plate Fracture Repair System to Treat Rib Fractures

Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to gather information about a device used to help fix broken ribs. Hypothesis: Rib fracture repair with the U-plate system is clinically durable and safe for the indications of flail chest repair, acute pain control, chest wall defect repair, and rib fracture non-union.