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Fractures, Bone clinical trials

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NCT ID: NCT01553630 Terminated - Tibial Fractures Clinical Trials

Reamed Locked Plating - Metaphyseal Fractures of the Distal Femur and Tibia

Start date: May 2010
Phase: N/A
Study type: Interventional

Comminuted metaphyseal fractures (OTA classification A2/3 and C2/3) of the distal femur and distal tibia are difficult to treat and typically have more complications than other metaphyseal fractures. Delayed union, nonunion and need for secondary bone graft procedures are frequent outcomes. These A2/3 and C2/3 fractures of the distal femur and distal tibia treated with locked plates often have a critical sized fracture gap (poorly organized cortical pieces many of which are stripped of soft tissue). Optimal management strategies that minimize both fracture healing time and complication rates remain controversial. Primary bone grafts or early secondary bone grafts have been recommended for these comminuted open fractures, but have not been studied as the primary end point in a randomized trial. There is a need to study primary bone grafting during open reduction and internal fixation (plating) of these difficult fractures, to determine if shorter healing time, and thus less need for reoperation, can be achieved. Hypothesis Acute autogenous bone grafting at the time of fixation will hasten clinical and radiographic union with a lower need for secondary procedures

NCT ID: NCT01550146 Unknown status - Clinical trials for Fractured Neck of Femur

Single Dose of Dexamethasone in Femur Fractures

Start date: July 2009
Phase: Phase 4
Study type: Interventional

Fracture neck of femur is a common cause of hospital admission in the elderly and requires operative fixation. Dexamethasone has the potential of inhibiting cortisol secretion. In addition, preoperative glucocorticoids improve analgesia and decrease opioid consumption with reduction in associated side effects in a variety of clinical settings. The investigators hypothesis was that a single dose of preoperative dexamethasone enhance postoperative analgesia and attenuates the inflammatory response in patients undergoing operative fixation of fractured neck of femur, in a prospective, randomized, placebo controled trial.

NCT ID: NCT01550094 Completed - Clinical trials for Crushing Injury of Lower Leg

A Comparison of Two Injection Locations in Obese Patients Having Lower Leg/Foot Surgery

Start date: March 2012
Phase: N/A
Study type: Observational

One technique for the nerve block involves injecting the numbing medicine where the nerve is together (higher up in the back of the thigh). The other technique involves injecting the numbing medicine where the nerve splits into two parts. By injecting numbing medication around the nerve(s), there will be less pain after the procedure. It is thought that the numbing medicine will be easier to inject in the group that the nerves are split. It is expected that subjects may need less pain medication and have lower pain ratings in this group too.

NCT ID: NCT01548456 Completed - Femoral Fractures Clinical Trials

Nails Versus Plates for Femur Fractures in Dar es Salaam, Tanzania

Start date: July 2012
Phase: N/A
Study type: Observational

This is a prospective observational study of patients with femur fractures in Dar es Salaam, Tanzania comparing two different surgical techniques: intramedullary nailing (IMN) and open reduction internal fixation (ORIF) with a plate. The primary outcome is the rate of reoperation for any reason, and the secondary outcomes are fracture healing, return to work, and health-related quality-of-life. The investigators hypothesize that there will be a difference in the rate of reoperation for patients with femur fractures treated with an IMN compared to ORIF with a plate.

NCT ID: NCT01547468 Withdrawn - Hip Fracture Clinical Trials

A Comparison of Two Pain Control Techniques on Deliruim in Hip Fracture Patients

Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is compare the rates of post-operative delirium between a group of people receiving intravenous (IV) pain control after hip fracture surgery and a group of people receiving a femoral nerve catheter for pain control. Post-operative delirium is confusion that can happen after the deep sleep of anesthesia. AThe hypothesis is that the group receiving the femoral nerve catheter for pain may have a lower incidence of delirium than the group receiveing IV pain medication.

NCT ID: NCT01544933 Completed - Clinical trials for Burst Thoracic Spine Fractures

The Influence of the Ribs on the Gravity of Burst Thoracic Spine Fractures

Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to analyse the anatomic influence of the ribs related to the incidence and severity of burst spine fractures.

NCT ID: NCT01542840 Not yet recruiting - Clinical trials for Crushing Injury of Lower Leg

Onset Time of Nerve Block: A Comparison of Two Injection Locations in Patients Having Lower Leg/ Foot Surgery

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

The purpose of this study is to compare injecting local anesthetic (numbing medication) in different patterns around a major nerve in the leg. Patients who undergo surgery to the lower leg and/or foot are usually offered the option of a nerve block to help with pain control after surgery. A nerve block involves injecting local anesthetic (numbing medicine) by a nerve or nerves that provide sensation to the area where surgery will be performed. The local anesthetic (numbing medication) numbs up the area where the surgery is performed and helps decrease the amount of pain felt after surgery. The local anesthetic (numbing medication) can be injected in various patterns by a nerve, such as in one spot by a nerve or completely surrounding a nerve. The local anesthetic will be either injected around the sciatic nerve or will injected in a way that will split the sciatic nerve into the two component nerves that make it up, the tibial and sciatic, and surrounds each nerve. The hypothesis is that subjects in the group that local anesthetic is injected in a pattern that separates the sciatic nerve into the two component nerves may have a faster onset time of regional anesthesia and block success than subjects in the group that have the local anesthetic injected at around the nerve.

NCT ID: NCT01537770 Completed - Clinical trials for Osteoporotic Fractures

Vertebroplasty Compared With a Sham-procedure for Painful Acute Osteoporotic Vertebral Fractures

VOPE
Start date: February 2012
Phase: Phase 4
Study type: Interventional

The main purpose of this study: - to determine whether vertebroplasty has a pain palliating effect superior to a sham-procedure for acute painful osteoporotic vertebral fractures of the thoracic and lumbar spine. Secondary purposes: - To determine if there are differences in the two methods on preventing forward tilting of the spine and/or shortening of the total height of the spine. - measure if there are differences in change of lung capacity between the two methods

NCT ID: NCT01537523 Not yet recruiting - Fracture Clinical Trials

To Investigate the Effect of Early Community-care Program on Fracture Hip Patient

Start date: February 2012
Phase: N/A
Study type: Interventional

The early community-care program is well-known rehabiliation for the fracture hip patient. For the discharged fracture hip patient from hospital, it is worth to investigate the effect of early mobilization program to improve their physical and psychological aspects.

NCT ID: NCT01535781 Terminated - Anemia Clinical Trials

Study of the Effect of Tranexamic Acid Administered to Patients With Hip Fractures. Can Blood Loss be Reduced?

Start date: September 2011
Phase: N/A
Study type: Interventional

The effect of Tranexamic acid on blood loss, hemoglobin and transfusions in patients with pertrochanteric hip fractures. Tranexamic acid is a well known drug used in many types of surgery. The investigators wish to investigate if the use of tranexamic acid can reduce the peri- and post-operative blood loss in patients who undergo surgery with a short intramedullary nail, for a pertrochanteric hip fracture. An interim analysis was planned when reaching 60 inclusions. The interim analysis was conducted only on the primary outcome (TBL). A difference in TBL of no less than 500 ml was considered a reason to halt the study. The 0.001 level was chosen as a simple approach to this interim analysis from the Haybittle-Peto boundary