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Fractures, Bone clinical trials

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NCT ID: NCT02202122 Withdrawn - Clinical trials for Femoral Neck Fracture

Interest of the OSA (Obstructive Sleep Apnea) Predictive Scores in the Prognosis of Postoperative Mortality of Femoral Neck Fractures

Start date: September 2014
Phase: N/A
Study type: Observational [Patient Registry]

Interest of the four major OSA Predictive Scores (STOP-BANG, P-SAP, DES-OSA, OSA50) in the prognosis of postoperative mortality after femoral neck fracture.

NCT ID: NCT02198820 Withdrawn - Clinical trials for Femoral Neck Fractures

Practice Survey on Femoral Neck Fractures and the Incidence of Type of Anesthesia on Patient Outcome

Start date: October 2014
Phase: N/A
Study type: Observational [Patient Registry]

Inclusion of all patients with femoral neck fracture presenting in Saint-Luc Bouge Hospital between October 1th 2014 and September 30th 2015. Comparison of severity scores of these patients and the scale of Nottingham on immediate (day 1 and day 2) and late (1 month) outcome.

NCT ID: NCT02196311 Withdrawn - Clinical trials for Supracondylar Humerus Fractures

Treatment Of Supracondylar Fractures Closed Reduction And Circular Ring External Fixation Versus Open Reduction and Internal Fixation

Start date: March 2014
Phase:
Study type: Observational

Patients treated with circular external fixation will have better outcomes (as measured by range of motion (ROM), alignment, outcome surveys) than those treated with open reduction and internal fixation (ORIF).

NCT ID: NCT02179697 Withdrawn - Spinal Fractures Clinical Trials

Randomized Trial With an Observational Component of Non-operative Versus Operative Treatment for AO Type A3 Fractures

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

The purpose of this study is to compare surgery plus bracing versus bracing alone. Both groups are considered standard of care treatments. The goal of this study is to determine which group is a better treatment.

NCT ID: NCT02094807 Withdrawn - Pain Clinical Trials

Pain as Indication for Operative Treatment of Traumatic Rib Fractures

potf
Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized controlled study is to determine whether acute and chronic pain in patients who suffer multiple traumatic rib fractures is decreased after surgical management as compared to conservative management.

NCT ID: NCT02093364 Withdrawn - Clinical trials for Failed Open Reduction Internal Fixation (ORIF) of a Radial Head Fracture

A Focused Registry to Document the Use of the Short- or Long-stemmed Radial Head Prosthesis (RHP)

Start date: July 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of this focused registry is to evaluate the clinical implications of the RHP position (relative to the articulations) regarding functional and radiographic parameters in patients treated with the RHP with a straight and curved stem.

NCT ID: NCT02091492 Withdrawn - Humeral Fractures Clinical Trials

Teriparatide for Fracture Repair in Humans

TERAFRAP
Start date: June 2014
Phase: Phase 3
Study type: Interventional

This study will test the hypothesis that daily subcuaneous administration of 20µg of teriparatide (TPTD) as compared to daily subcuaneous placebo for twelve weeks accelerates proximal 2-segment humerus fracture healing and improves the three dimensional structural properties of bone as measured via quantitative bone image analysis and finite element modeling assessed by quantitative computed tomography.

NCT ID: NCT01940536 Withdrawn - Hip Fracture Clinical Trials

The Effect of Tranexamic Acid on Transfusion Rates in Intertrochanteric Hip Fractures

Start date: December 2015
Phase: Phase 4
Study type: Interventional

The goal of this study is to determine if the use of tranexamic acid, a safe and effective antifibrinolytic, in patients with intertrochanteric hip fractures will result in a reduction in blood transfusion rates. Treatment will be administered pre-operatively as well as at the time of surgical incision. The primary outcome will be need for blood transfusion. Secondary outcomes will include calculated perioperative blood loss, length of stay, cost of inpatient care, and rate of adverse events, including DVT, PE, infection, MI, cerebrovascular event, need for re-hospitalization or re-operation and 30 day mortality.

NCT ID: NCT01923623 Withdrawn - Clinical trials for Ankle Fracture in Need of Surgical Fixation

The Effect of Nerve Blockades in Addition to General Anesthesia in Surgical Fixation of Ankle Fractures.

Start date: July 1, 2013
Phase: Phase 4
Study type: Interventional

This clinical, randomized, and controlled study will provide valuable scientific evidence regarding the effect of adding peripheral nerve blockades to general anaesthesia during ankle surgery. In particular, the investigators want to determine if the need for postoperative opioids will be reduced and whether this will lead to shorter admission to recovery room and fewer instances of side effects such as postoperative nausea and vomiting. In addition, the investigators will determine whether the functional outcome is improved i.e. faster and more successful rehabilitation. This would have profound benefits not only to the individual patient but also to society by reducing expenses during admission, the cost of sick leave etc.

NCT ID: NCT01812863 Withdrawn - Humeral Fractures Clinical Trials

Pain Management in Children Undergoing Supracondylar Humerus Fracture Repair

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

The purpose of this study is to determine if US-guided supraclavicular anesthetic blocks reduce postoperative pain, use of rescue medication, and improve functional outcomes in children who underwent surgery for supracondylar humerus fractures.