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Fractures, Bone clinical trials

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NCT ID: NCT02578095 Completed - Hip Fractures Clinical Trials

Acute Hip Fracture Study in Patients 65 Years or Greater

Start date: October 30, 2015
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, parallel group, placebo-controlled, multicenter study to investigate the safety, tolerability, and efficacy of VK5211 after 12 weeks of treatment. Males and females ≥65 years old who are ambulatory and recovering from a hip fracture will be eligible for participation 3-7 weeks post-injury.

NCT ID: NCT02566018 Completed - Humeral Fractures Clinical Trials

Treatment of Proximal Humerus Fractures in the Elderly

prox_hum
Start date: May 1, 2015
Phase:
Study type: Observational

This study is set to evaluate a proposed standard for the treatment of proximal humerus fractures

NCT ID: NCT02556658 Completed - Clinical trials for Hip Fracture Surgery

Predicted Level of General Anaesthesia in Hip Fracture Surgery

NAPfem
Start date: February 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate if prediction of general anaesthesia level by the Smartpilot® View device can improve the quality of anaesthesia in patients undergoing hip fracture surgery.

NCT ID: NCT02554500 Completed - Clinical trials for Fractured Scaphoid Bone

Bone Microcirculation After Remote Ischemic Preconditioning

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

In trauma surgery and hand surgery treatment strategies of none healing bone fractures aim at replacing pseudarthrosis by well vascularized bone and improving microcirculation. Although previous studies indicate that remote ischemic preconditioning (RIPC) can accelerate bone healing in case of non-union, only a few studies focused on the elucidation of its mechanisms of action. Therefore, the aim of this study is to evaluate the microcirculatory effects of remote ischemic preconditioning (RIPC) on scaphoid bones and metacarpal bones and metatarsal bones in a human in-vivo setting for the first time.

NCT ID: NCT02551315 Completed - Clinical trials for Type 2 Diabetes Mellitus

Microarchitecture, Bone Strength and Fracture Risk in Type 2 Diabetes

DiabOS
Start date: June 2016
Phase:
Study type: Observational

This multicenter, prospective, observational cohort study will assess bone differences in women and men with type 2 diabetes mellitus (T2DM) with and without fragility fractures.

NCT ID: NCT02539173 Completed - Shoulder Fractures Clinical Trials

Diagnosis of Diaphragmatic Paralysis After Interscalene Block: Feasibility and Impact Observed

BBDDIAPHRAGM
Start date: June 1, 2014
Phase: N/A
Study type: Interventional

1. INTRODUCTION AND MAIN OBJECTIVES The incidence of diaphragmatic paralysis after an inter-block scalénique varies between 30 and 100% in the literature. Its clinical impact is mostly absent and paralysis regresses after the block lifted. When it is suspected, it can be diagnosed by a chest radio, showing an elevation of the dome. The objective of this study is to evaluate the incidence of diaphragmatic paralysis by measuring the thickness diaphragmatic as quantitative assessment of diaphragmatic contraction noninvasive ultrasound scan and feasibility of this measure in SSPI unit (post-interventional monitoring unit) with scan (ultrasound) in the usual way used for the block under ultrasound scan. 2. STUDY TYPE Prospective, single-center clinical study routine care involving 50 consecutive patients scheduled to undergo surgical procedures in the area of the shoulder or arm for which locoregional analgesia inter-block type scalénique or supraclavicular ultrasound scan is indicated below. 3. START OF THE STUDY February 2014 with an expected duration of six months.

NCT ID: NCT02536898 Completed - Hip Fracture Clinical Trials

Norwegian Capture the Fracture Initiative

NoFRACT
Start date: May 2015
Phase: N/A
Study type: Interventional

The main aim is to assess the effectiveness of introducing a standardized intervention program for treatment of patients with a fragility fracture as measured by changes in the fracture rates and the mortality.

NCT ID: NCT02535624 Completed - Fractures, Bone Clinical Trials

Retroperitoneal Packing or Angioembolization for Hemorrhage Control of Pelvic Fractures

Start date: February 2003
Phase: N/A
Study type: Interventional

This study is designed to answer whether minimal invasive vessel clotting (angioembolization) or open surgery (retroperitoneal packing) is more effective for pelvic fractures with massive bleeding. Patients admitted at daytime (7am-5pm) are treated with angioembolization while patients admitted at nighttime (5pm to 7am) are treated with open surgery.

NCT ID: NCT02534259 Completed - Tibial Fractures Clinical Trials

Mobile Monitoring of Fracture Healing

Start date: August 2015
Phase:
Study type: Observational

The objective of this study is to develop methods for using forces measured on circular external fixators to predict the state of individual patient's healing of severe tibial fractures and defects.

NCT ID: NCT02522403 Completed - Radius Fracture Clinical Trials

Acupuncture in Distal Radius Fracture Patients

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

The patients with distal radius fracture treated with immobilization (cast) and percutaneous pinning it will be to able to participate in this randomized trial. The investigators will be able to determine if the laser acupuncture is a good therapy for the rehabilitation in this type of patients. And if they are more comfortable to begin his rehabilitation exercise after the application of this therapy