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NCT ID: NCT03404869 Recruiting - CDG Ib Clinical Trials

Study of ORL-1M in Patients With CDG-Ib

Start date: March 31, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Study of ORL-1F in Patients With CDG-Ib

NCT ID: NCT03404856 Recruiting - Clinical trials for Glycogen Storage Disease, Type 14

Study of ORL-1G in Patients With Glycogen Storage Disease Type 14

Start date: October 31, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

Study of ORL-1G in Patients With Glycogen Storage Disease Type 14

NCT ID: NCT03402581 Recruiting - Clinical trials for Difficult Airway, Videolaryngoscopes

The Effect of Different Videolaryngoscopes on Intubation Success in Obese Patients

Start date: September 2, 2018
Phase: N/A
Study type: Observational [Patient Registry]

Obese patients may have difficulty in airway management.Patients who have body mass index > 35 are challenging patients for anesthesiologist. Short neck, more adipose tissue may be reasons for airway difficulty. Videolaryngoscopes are devices that ease the management of difficult airway.This study is designed to evaluate the differences and the effects of different laryngoscopes.

NCT ID: NCT03400735 Recruiting - Clinical trials for Acute Exacerbation of Chronic Bronchitis

Comparison of Cefdinir and Cefdinir/Clavulanic Acid Combination in Adults

Start date: November 1, 2017
Phase: Phase 4
Study type: Interventional

It is planned to compare the efficacy and safety of cefdinir and cefdinir/clavulanic acide treatments in acute exacerbation of chronic bronchitis (AECB) and community-acquired pneumoniae (CAP) patients.

NCT ID: NCT03400670 Recruiting - Ventilatory Failure Clinical Trials

Comparison of Two Different NCPAP Methods in Preterm Infants With Respiratory Distress Syndrome

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

is to compare introduction of two different NCPAP methods in terms of mechanical ventilation (MV) need (non-invasive respiratory support failure) and surfactant need within the first 72 hours of life in preterm infants with Respiratory Distress Syndrome (RDS) at 26-30 weeks of gestation.

NCT ID: NCT03400358 Recruiting - Clinical trials for Medical; Abortion, Fetus

Uterocervical Angle in the Pregnancy Termination of Multiparous Women

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

To evaluate the uterocervical angle (UCA) in the prediction of second trimester termination success of multiparous women.

NCT ID: NCT03399890 Completed - Clinical trials for Neurological Complication

The Influence of Neuromuscular Reversal on Neurological Physical Exam Time in Lumbar Neurosurgical Cases.

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

Neurological physical exam is a very important outcome that should be evaluated as soon as possible after every lumbar procedures. The aim of this study was to evaluate the neurological physical examination time after lumbar procedures.

NCT ID: NCT03398239 Completed - Clinical trials for Hypercapnic Respiratory Failure

Comparison of BPAP ST/T and BPAP ST / T Mode With AVAPS for Hypercapnic Respiratory Failure in ED

Start date: October 20, 2016
Phase: N/A
Study type: Interventional

The aim of the present study; To compare the effects of respiratory support options available for NIMV at the emergency department; i.e. AVAPS and ST/T modes, on the patient's pCO2 values, additional treatment need (another non-invasive ventilation method or endotracheal intubation) and the duration of stay in hospital.

NCT ID: NCT03397849 Not yet recruiting - Primary Prevention Clinical Trials

Lifestyle Intervention Using Mobile Technology in Patients With High Cardiovascular Risk

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

In the present study, investigators aim to compare intervention using mobile technology (IMT) plus usual care with only usual care in patients with a high risk for cardiovascular diseases (CVD). Investigators hypothesize that IMT plus usual care reduces the CVD risk and improves the secondary outcomes in this population through 12 months of follow-up period. Patients presented to the outpatient clinics in a tertiary hospital (Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Research and Training Hospital, Istanbul, Turkey) who were considered to be eligible according to inclusion and exclusion criteria will be enrolled to the study. The eligibility criteria is; Patients between 20 to 79 years old who are in high risk for CVD (10 years ASCVD risk ≥ 7.5%). Patients with prior CVD events (myocardial infarction, percutaneous coronary intervention, coronary artery by-pass grafting operation, stroke and peripheral artery disease), pregnancy, communication problems, severe neuropsychiatric problems and chronic kidney disease are excluded from the study. In addition, patients that are unable to use smartphone phone are also excluded.

NCT ID: NCT03395496 Completed - Dental Caries Clinical Trials

Comparison of Biodentine and MTA Pulpotomies in the Primary Molar Teeth 3 Year Follow up

Start date: May 1, 2013
Phase: Early Phase 1
Study type: Interventional

The aim of this study is to compare two pulpotomy medicaments in primary molars clinically.A total of 200 primary molars with deep caries were treated with two different pulpotomy medicaments (Mineral Trioxide Aggregate and BiodentineTM) in this study. The inclusion criteria for tooth selection were no clinical and radiographic evidence of pulp pathology. During 36 months of follow-up at 3-month intervals, clinical and radiographic success and failures were recorded.