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NCT ID: NCT03249545 Recruiting - Ablation Clinical Trials

Late Effect of Ablation on Premature Ventricular Complex Ablation

Start date: July 1, 2017
Phase: N/A
Study type: Observational

Premature Ventricular Complex (PVC) ablation is performed in certain indications. Generally acutely abolition of PVC at the time of ablation accepted as successful ablation. However in some patients this effect occurs lately. In this study investigators sought late effect of ablation

NCT ID: NCT03247426 Not yet recruiting - Physical Activity Clinical Trials

Sleep Quality, Job Satisfaction, Quality of Life, Occupational Burnout Levels in Individuals

Start date: August 10, 2017
Phase: N/A
Study type: Observational

The aim of this study is to compare sleep quality, job satisfaction, quality of life, occupational burnout levels among individuals who do or do not do exercise.

NCT ID: NCT03245502 Recruiting - Clinical trials for Disorder; Heart, Functional, Postoperative, Cardiac Surgery

The Effect of Blood Transfusion on Venoarterial pco2 Difference in Cardiac Surgery

Start date: August 15, 2017
Phase: N/A
Study type: Observational

Venoarterial CO2 difference, (delta CO2) lactate, pH will be recorded in several steps in valvular and coronary artery bypass graft operations. The patients will be divided in two groups as Transfusion and No Transfusion Groups observationally. The trend of delta CO2, postoperative complications and 28 days mortality will be compared.

NCT ID: NCT03244748 Recruiting - Clinical trials for Ventricular Tachycardia

Amiodarone Usage After Ischemic Ventricular Tachycardia Ablation

Start date: January 1, 2016
Phase: N/A
Study type: Observational [Patient Registry]

Ventricular Tachycardia ablation in ischemic cardiomyopathy patients is required procedure in cases when anti-arrhythmic drugs failed. The concern is if adjunctive continuation amiodarone after ablation is needed.

NCT ID: NCT03241615 Recruiting - Clinical trials for Neurogenic Dysphagia

Dysphagia Symptom Severity and Quality of Life

Start date: August 8, 2017
Phase: N/A
Study type: Observational

The aim of the study is to investigate the relationship between dysphagia symptom severity and quality of life of the patients with neurogenic dysphagia.

NCT ID: NCT03241160 Recruiting - Cerebral Palsy Clinical Trials

Chewing Disorders, Gross Motor Function and Trunk Control in Cerebral Palsy

Start date: August 5, 2017
Phase: N/A
Study type: Observational

The study is planned to determine the relationship between chewing performance level and gross motor function, and trunk postural control in cerebral palsy (CP).

NCT ID: NCT03240367 Completed - Obesity, Morbid Clinical Trials

Comparison of Stapler Line Bleeding Control Techniquessurgery

Start date: December 4, 2016
Phase: N/A
Study type: Interventional

Introduction RYGB surgeon; Have become increasingly morbid obesity treatment methods with improvements in minimally invasive surgery. Ensuring patient comfort and early return to life are the criteria that should be given priority in this treatment method.The purpose of this study; Emphasizing that the cautery technique of the stapler line bleeding control methods is as successful as the other methods.

NCT ID: NCT03239925 Recruiting - Clinical trials for Acute Effects of EMWs Emitted by Cell Phones

Acute Effects of Cell Phone Exposure on Immediate Attention Levels and Concentration of Emergency Physicians

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

To investigate the acute effects of cell phone exposure on immediate attention levels and concentration of emergency department physicians

NCT ID: NCT03239301 Completed - Clinical trials for Spinal Cord Injury Cervical

Robotic-assisted Upper Extremity Training in Spinal Cord Injury Patients

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Study design: Controlled Trial Objective: To evaluate the effectiveness of robotic-assisted training of forearm and hand functions in spinal cord injury patients Setting: Ankara Physical Medicine and Rehabilitation Training and Research Hospital, Turkey Methods: Forty patients were allocated into robotic and control groups. Both groups received conventional rehabilitation program for four weeks. Moreover, robotic group received robotic rehabilitation program tailored to the patient five times a week (each session of 30 min). Baseline data and post-intervention data was compared.

NCT ID: NCT03238287 Not yet recruiting - Clinical trials for Cardiopulmonary Resuscitation

Manual and Mechanical Chest Compression During In-hospital Witnessed Cardiac Arrests Using Cerebral Oximetry

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Post-resuscitation neurological impairment is associated with morbidity and especially with late mortality. Thus, because good neurological outcome is vital for a successful resuscitation, it is essential to have sufficient cerebral tissue perfusion and oxygenation during its application. Near-Infrared Spectroscopy (NIRS) is used to evaluate such conditions. NIRS is a non-invasive technique which provides real-time, continuous information about regional cerebral tissue oxygen saturation levels (regional SO2/rSO2). Research on NIRS has been done in many studies including cardiovascular surgery, neurosurgery and their intensive care processes and its effectiveness has been approved. However, there is limited data on its use in cardiac arrests. As stated in the current guidelines, sufficient speed and depth of chest compressions, few interruptions of compressions are key to a successful outcome of resuscitation. The studies with the mechanical chest compression devices showed that the earlier it was applied in out-of-hospital cases, the higher the rates of survival until hospitalization. There is not sufficient number of studies on the routine use of mechanical chest compression devices for in-hospital cases. In case the application of manual resuscitation is not convenient (during patient relocation, procedure at the angiography laboratory, and rush hours of emergency services when staff might fall short), alternative methods will be required. The aim of our study is to compare rSO2 levels measured during resuscitation with manual and mechanical devices in in-hospital (at the emergency department) witnessed cardiac arrest cases and to analyze the impact of both application method and perfusion levels on survival and neurological outcome.