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Shoulder Fractures clinical trials

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NCT ID: NCT02608801 Completed - Hip Fractures Clinical Trials

Prediction and Secondary Prevention of Fractures

NOFRACTsub
Start date: April 2015
Phase:
Study type: Observational

The purpose of this study is to investigate patient related factors that contribute to increased risk of recurrent fractures and to investigate patient adherence to prescribed anti-osteoporotic drugs.

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: NCT02472314 Completed - Clinical trials for Fracture of Shoulder and Upper Arm

Exparel for Postoperative Pain Management in Shoulder Surgery

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

The purpose of this study is to compare the effect of liposomal Bupivacaine infiltration into the shoulder to continues nerve block with Bupivacaine on postoperative pain control and functional outcomes.

NCT ID: NCT02465398 Completed - Fracture Clinical Trials

Anatomical Shoulderâ„¢ Fracture PMCF Study

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

The purpose of this study is to obtain outcomes data on the Anatomical Shoulder Fracture System by analysis of standard scoring systems and radiographs. Outcome data will be collected using the following standard scoring systems: - Constant and Murley Score - Oxford Shoulder Score - EQ-5D (EuroQol)

NCT ID: NCT02425267 Completed - Clinical trials for Humeral Fractures, Proximal

Effectiveness of a Home Telerehabilitation Program for People With Proximal Humerus Fracture

TeleFracture
Start date: June 2015
Phase: N/A
Study type: Interventional

The main objective of the study is to compare the clinical effects of the innovative telerehabilitation approach (TELE group) compared to face-to-face visits to a clinic (CLINIC group) for patients treated for a proximal humerus fracture.

NCT ID: NCT02182752 Completed - Clinical trials for Shoulder Dislocation

The Effect of Tramadol on Interscalene Brachial Plexus Block

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of our study is to evaluate the effect of tramadol as an adjunct to ropivacaine local anesthetic solution in interscalene brachial plexus block for shoulder surgery.

NCT ID: NCT02122315 Completed - Clinical trials for Rotator Cuff Tear Surgical Repair

Dry Needling in Post-operative Shoulder Pain

Start date: February 2013
Phase: N/A
Study type: Interventional

Fractures of the proximal humerus account for between 5% and 8% off all reported fractures. Post-operative shoulder pain is highly frequent. Due to either surgical procedure, soft tissues surrounding the shoulder area can be damaged. The purpose of the current clinical trial was to compare the effects of physiotherapy versus physiotherapy plus TrP-DN on pain and function in patients who exhibit post-operative shoulder pain after a PHILOS procedure for proximal humeral fixation or rotator cuff tear repair.

NCT ID: NCT02052206 Completed - Clinical trials for Osteoarthritis of the Shoulder

Reconstruction of Complex Proximal Humeral Fractures.

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

The purpose of this study is to evaluate the accuracy of shoulder replacement surgery in realization a computer assisted 3D planning compared to conventional 2D planning.

NCT ID: NCT01984112 Completed - Wounds and Injuries Clinical Trials

Proximal Humerus Fractures: Randomized Study Between Locking Nails and Locking Plates for Neer 2 and 3 Parts

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

The hypothesis of this study is to determine whether the technique of intramedullary locking nail presents clinical results comparable to the technique of locking plates, based on the Constant Score.

NCT ID: NCT01737385 Completed - Clinical trials for Proximal Humeral Fractures

Examination of Microcirculation of the Caput Humeri After Proximal Humerus Fracture

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

This study examines the microcirculation of the caput humeri after proximal humeral fracturation using O2C light probes. During the operation the blood circulation is measured at four points (tuberculum majus, tuberculum minus, neck and head of the humerus) directly on the bone. The O2C light probes are a none-invasive technique of measuring blood flow, velocity and oxygen concentration. The data is analysed in respect to the fracture type according to the classification of Neer. Valuable additional information for the correct treatment and prognosis of humeral fractures is expected.