Clinical Trials Logo

Tibial Fractures clinical trials

View clinical trials related to Tibial Fractures.

Filter by:

NCT ID: NCT00387686 Terminated - Fractures Clinical Trials

A Phase 2/3 Multicenter, Controlled Trial Of rhBMP-2/CPM In Tibial Fractures

Start date: November 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of this study is to assess whether a single dose of rhBMP-2/CPM administered at the fracture site via percutaneous injection, in combination with standard of care, accelerates fracture union and return to normal function in subjects who have a closed diaphyseal tibial fracture when compared to standard of care alone.

NCT ID: NCT00365573 Suspended - Tibial Fracture Clinical Trials

Doppler Ultrasonography Evaluation of Tibial Fracture Site Vascularity

Start date: February 2008
Phase: Phase 2
Study type: Observational

The purpose of this study is to evaluate the blood supply to patients that are suffering from fracture in the tibia by UltraSound Doppler.

NCT ID: NCT00264511 Completed - Tibial Fracture Clinical Trials

Hyperbaric Oxygen in Lower Leg Trauma

Start date: February 13, 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Study hypothesis :Hyperbaric Oxygen may prevent complications and improve outcomes in severe lower limb trauma. We propose to investigate this hypothesis by conducting an International multi centre randomised control trial of standard trauma/orthopaedic care with or without a concurrent course of hyperbaric oxygen treatments.

NCT ID: NCT00254514 Completed - Bone Fracture Clinical Trials

Controlled Study to Evaluate the Efficacy and Safety of the Treatment With Growth Hormone in Tibia Fractures

Start date: August 2001
Phase: Phase 2
Study type: Interventional

This trial is conducted in Africa, Europe and Middle East. This trial investigates the efficacy and safety of three dose levels of Norditropin® (growth hormone) as compared to placebo in the treatment of tibia fractures. The trial will be conducted in two parts: in the first part, the patients will be evaluated with regard to efficacy (fracture healing) and safety at short time intervals until week 24 post-surgery. In the second part, long-term safety and fracture healing up to 12 months post-surgery will be evaluated.

NCT ID: NCT00253981 Terminated - Tibial Fractures Clinical Trials

Light Therapy in the Treatment of Leg Pain

MilCAM
Start date: November 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to apply Anodyne therapy to active duty soldiers, who have shin splints, to evaluate healing time and effectiveness.

NCT ID: NCT00250302 Completed - Tibial Fracture Clinical Trials

Autologous Implantation of Mesenchymal Stem Cells for the Treatment of Distal Tibial Fractures

Start date: April 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Mesenchymal stem cells are found in bone marrow, and have the ability to differentiate into different tissue types. The primary objective of the study is to examine the safety of using such cells to treat patients suffering from distal tibial shaft fractures. The cells will be isolated from the patient's bone marrow, loaded onto a carrier and implanted locally at the fracture site.

NCT ID: NCT00240396 Withdrawn - Femur Fracture Clinical Trials

Bimodal Analgesia as Form of Pain Control Post Long Bone Fracture

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized study is to evaluate the risks and benefits of using bimodal analgesia, (i.e. Narcotics and NSAIDS) vs Narcotics alone post long bone fracture.

NCT ID: NCT00161616 Completed - Tibial Fractures Clinical Trials

Study Evaluating InductOs in Diaphyseal Tibia Fractures

Start date: September 2003
Phase: Phase 4
Study type: Interventional

Demonstrate a larger proportion of subjects with healed fractures among subjects treated with InductOs and reamed, locked intramedullary nailing compared to subjects treated with reamed, locked intramedullary nailing alone.

NCT ID: NCT00127725 Recruiting - Tibial Fractures Clinical Trials

Pulsed Electromagnetic Field (PEMF) Stimulation for Tibia Fractures

Start date: August 2005
Phase: Phase 2
Study type: Interventional

Fractures of the tibial shaft (diaphysis) are some of the most common long bone fractures. They most frequently occur in males less than 40 years of age. Despite advancements in the surgical management of these fractures, the precarious blood supply and lack of soft-tissue cover of the shaft of the tibia make these fractures vulnerable to non-union and infection. These complications often require multiple procedures, extended time off of work, and can result in ongoing poor mobility. This is reflected in the surgical revision rate that the scientific literature has recorded as being between 20 and 30%. Pulsed electromagnetic field (PEMF) stimulation has been shown to be a safe and effective treatment for non-unions of the tibia. These are fractures in which the bone has failed to unite and the healing process has ceased. The PEMF is delivered via a device such as the EBI Bone Healing System®, which straps onto the limb overlying the fracture. It is lightweight and portable using a rechargeable battery for power. It is compatible with internal and external fixation and may also be worn over a plaster or fibreglass cast. It is usually kept in place for ten hours per day and used for a period of three months or until the fracture unites. In animal models, PEMF stimulation has been demonstrated to improve the time to fracture healing in acute fractures. There have been no demonstrated side effects of the therapy. The study hypothesis is that PEMF stimulation during the first twelve weeks after fracture, in addition to normal surgical care, will increase the union rate for these fractures and thereby significantly reduce the surgical revision rate within the first twelve months following fracture.

NCT ID: NCT00038129 Completed - Tibial Fracture Clinical Trials

SPRINT - Randomized Trial of Tibial Fracture Fixation

Start date: May 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if there is a difference in the rate of healing of a tibia fracture treated with an intramedullary nail based on whether or not the bone was reamed prior to nail insertion.