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NCT ID: NCT03470545 Completed - Clinical trials for Obstructive Hypertrophic Cardiomyopathy

Clinical Study to Evaluate Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy

EXPLORER-HCM
Start date: May 29, 2018
Phase: Phase 3
Study type: Interventional

This is a multicenter, international, double-blind study of the administration of mavacamten in participants with symptomatic obstructive HCM (oHCM). Approximately 220 participants will be randomized to receive placebo or mavacamten.

NCT ID: NCT03470454 Completed - Diabetes Clinical Trials

Contrast Nephropathy in Type 2 Diabetes

VCG4
Start date: July 1, 2018
Phase:
Study type: Observational [Patient Registry]

To study the effect of radiocontrast material on kidney functions in diabetics with microalbuminuria

NCT ID: NCT03470311 Completed - Clinical trials for Severe Prednisone Dependent Eosinophilic Asthma

Benralizumab in Patients With Inadequate Response to Anti-IL5 Monoclonal Antibody Therapies

Start date: April 26, 2018
Phase: Phase 3
Study type: Interventional

In severe prednisone-dependent eosinophilic asthma, Benralizumab would suppress airway eosinophilia that is not suppressed by either Mepolizumab or Reslizumab and this would be associated with greater asthma control

NCT ID: NCT03470233 Completed - Clinical trials for Multi-drug Resistant Tuberculosis

Post Marketing Registry to Assess Usage, Safety and Effectiveness of Deltyba Tablets in Korean Patients With MDR-TB

Start date: May 25, 2017
Phase:
Study type: Observational

Deltyba Registry aims to collect the usage information of Deltyba which could be a factor of developing resistance in actual clinical settings.

NCT ID: NCT03470155 Completed - Clinical trials for Mitral Valve Insufficiency

Operative Mitral Valve Reconstruction in Functional mv Insufficiency With Reduced Systolic Ventricle Function

REFORM-MR
Start date: June 5, 2018
Phase:
Study type: Observational [Patient Registry]

Functional mitral insufficiency poses a challenge with regard to the optimal time of intervention, particularly because they are frequently associated with left ventricular (LV) dilation and reduced LV ejection fraction (EF). The registry will document the underlying pathology by using transthoracal echo cardiography (TTE) with analysis of common tenting parameters. OP strategies, data and outcomes will be documented, as well as follow-up data for echocardiography, quality of life and MACCE outcomes after 6 months, 1 and 2 years.

NCT ID: NCT03470012 Completed - Clinical trials for Skin (FLACC Scores of Test Subjects) After Tape Removal

Adhesive Tape Trauma Evaluation of a New Gentle Tape in Healthy Infant Subjects

Start date: January 16, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to determine the relative gentleness of a new medical tape.

NCT ID: NCT03469843 Completed - Clinical trials for Congenital Heart Disease

Characterization of the Cardiac Reinnervation of Patients With Transposition of the Great Arteries Long After Repair With the Arterial Switch Operation. Correlation With Electrocardiographic and Exercise Test Parameters

Start date: April 19, 2018
Phase:
Study type: Observational

Cardiac denervation is inherent to the arterial switch (ASO) technique for the repair of transposition of the great arteries (TGA) and the long term reinnervation process has not been studied. We sought to describe the reinnervation status of adult patients long after the ASO, to identify areas of myocardial perfusion/innervation mismatch and to assess the relation of innervation status and exercise capacity.

NCT ID: NCT03469648 Completed - Clinical trials for Patients With ASA Status I-III Scheduled for Surgery

Intraoperative Air-Test

Start date: March 10, 2018
Phase:
Study type: Observational

Although imaging techniques are the reference standard to diagnose alveolar collapse, in the postoperative period and using the peripheral hemoglobin oxygen saturation (SpO2), a non-invasive simple and accurate test (Air-Test) was recently validated to diagnose alveolar collapse. The aim of this study is to non-invasively describe the incidence of intraoperative atelectasis with the Air-Test in an unselected surgical population. In addition, we attempt to describe the association between positive Air-Test and the patient´s preoperative or intraoperative variables.

NCT ID: NCT03469635 Completed - Bariatric Surgery Clinical Trials

Nutritional Status During Pregnancy After Bariatric Surgery

PREGNUTRIBAR
Start date: January 2006
Phase:
Study type: Observational

Background: There is a lack of evidence on whether maternal nutritional deficiencies after Roux-en-Y gastric bypass (RYGB) or sleeve gastrectomy (SG) affect fetal development. The investigators hypothesis is that SG could induce nutritional deficiencies during pregnancy, as RYGB does, because of food restriction. These nutritional deficiencies may alter fetal growth. Methods: Women with singleton pregnancies who had at least one nutritional evaluation during pregnancy in our institution between 2006 and 2017 were included. The investigators evaluated nutritional deficiencies according to standard and pregnancy-specific norms. They have planned to study the relationships between these parameters and fetal growth. Objectives: To compare maternal nutritional parameters and neonatal outcomes after RYGB and SG and to assess the impact of nutritional alterations on fetal growth.

NCT ID: NCT03469570 Completed - Abdominal Surgery Clinical Trials

Assisted Fluid Management IDE Study

AFM
Start date: April 19, 2018
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the performance of the Acumen™ Assisted Fluid Management (AFM) Feature in its ability to predict a subject's fluid responsiveness.