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NCT ID: NCT02395237 Withdrawn - Healthy Clinical Trials

COMPOUND (INN): HOE490O - GLIMEPIRIDE / METFORMIN HCl (Amaryl® M)0 (Glimepiride/Metformin Hydrochloride Immediate Release Combination Tablet) in Fed Conditions in Healthy Male and/or Female Subjects.

Start date: May 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess, after single oral administration under fed conditions, the bioequivalence between the two batches of the same glimepiride/metformin hydrochloride (HCl) 2 mg/1000 mg fixed dose combination (FDC) tablets (immediate release combination tablet Amaryl® M IR 2/1000) manufactured in India and in Turkey.

NCT ID: NCT02385162 Withdrawn - Clinical trials for Glycogen Storage Disease Type II

Biomarker for Glycogen Storage Diseases (BioGlycogen)

BioGlycogen
Start date: August 20, 2018
Phase:
Study type: Observational

Development of a new MS-based biomarker for the early and sensitive diagnosis of Glycogen Storage Diseases from plasma. Testing for clinical robustness, specificity and long-term stability of the biomarker.

NCT ID: NCT02382224 Withdrawn - Clinical trials for Generalized Anxiety Disorder

Worry Exposure for Generalized Anxiety Disorder

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the efficacy of a worry exposure intervention, a form of cognitive behavioral therapy (CBT), in comparison to a waitlist condition for the treatment of Generalized Anxiety Disorder. There will be a total of 60 subjects enrolled at the University of Texas at Austin. Patients will be randomized (like a flip of a coin) to either 12-sessions of WE therapy or a 12-week waitlist before being offered entry into therapy.

NCT ID: NCT02340702 Withdrawn - Disease Clinical Trials

Chronic Obstructive Pulmonary Disease (COPD) in Patients Hospitalized for Acute Decompensated Heart Failure.

COPD
Start date: August 2014
Phase:
Study type: Observational [Patient Registry]

The presence of chronic obstructive pulmonary disease (COPD) would confer increased in-hospital mortality and length of hospital stay in patients with acute decompensated heart failure Assess the (1) prevalence of COPD in patients who are hospitalized for acute decompensated heart failure and (2) the association between COPD and in-hospital mortality or length of stay in this cohort.

NCT ID: NCT02247986 Withdrawn - Conduct Disorder Clinical Trials

Investigating the Impact of Methylphenidate on Neural Response in Disruptive Behavioral Disorder

Start date: September 4, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Background: - Disruptive behavior is a common problem for children and adolescents. It can be treated with some success with stimulant medicine. Researchers want to learn more about how this works. Objective: - To learn how the brain changes when taking the medicine methylphenidate for behavior problems. Eligibility: - Children ages 10 17 with conduct disorder and/or attention deficit disorder. - Healthy volunteers the same age. Design: - Participants will be screened under a separate protocol. - Participants will have two 3-hour sessions at the clinic. Girls who are menstruating will have a pregnancy test before their scans. - Visit 1: All participants will: - Perform simple tests on a computer. - Fill out a questionnaire along with their parent or guardian. - Have an MRI scan. A magnetic field and radio waves take pictures of the brain. Participants will lie on a table that slides into a metal cylinder. A coil will be placed over their head. They will be in the scanner for 60 minutes, lying still or performing a simple task. They will practice the task before the scan. A computer screen will show them task information during the scan. The scanner makes loud knocking sounds. Participants will get earplugs. Their parent or guardian can stay with them during the scan. - Only participants with behavior disorders will: - Take a pill of the study medicine or placebo. - Be monitored for any side effects. - Visit 2 is a repeat of Visit 1, except participants who got a pill in Visit 1 will get the other pill in Visit 2. For healthy volunteers, the 2 visits are exactly the same.

NCT ID: NCT02245776 Withdrawn - Clinical trials for Neurological; Disorder, Nervous System

Stem Cell Therapy in Incurable Neurological Disorders

Start date: December 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study was to analyze the benefit of autologous mononuclear cell therapy in incurable neurological disorders.

NCT ID: NCT02238730 Withdrawn - Depression Clinical Trials

Ultrabrief Right Unilateral and Brief Pulse Bitemporal Electroconvulsive Therapy

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

To evaluate the equivalent efficacy of ultrabrief pulsewidth right unilateral electroconvulsive therapy versus bitemporal brief pulse electroconvulsive therapy in the treatment of depression and to evaluate the cognitive effects of ultrabrief right unilateral electroconvulsive therapy versus bitemporal brief pulse electroconvulsive therapy.

NCT ID: NCT02226458 Withdrawn - Clinical trials for Autism Spectrum Disorder

An Exploratory Open Label Study of EPI-743 (Vincerinone TM) in Children With Autism Spectrum Disorder

Autism
Start date: October 31, 2014
Phase: Phase 2
Study type: Interventional

The investigators hypothesize that EPI-743 may provide clinical benefit to children with Autism Spectrum Disorder.

NCT ID: NCT02212613 Withdrawn - Clinical trials for Major Depressive Disorder and Irritability

Brexpiprazole (OPC 34712) Trial in the Treatment of Adults With Major Depressive Disorder and Irritability

Start date: September 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to explore the effects of fixed-dosed brexpiprazole adjunctive treatment in subjects with Major Depressive Disorder with irritability

NCT ID: NCT02212275 Withdrawn - Clinical trials for Autism Spectrum Disorders

Cortical Metrics in Intervention Trials With Autism Spectrum Disorders

Start date: August 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators overarching aim is to obtain preliminary data to support a larger grant to validate a novel objective, physiologically-based outcome measure for clinical trials in autism spectrum disorders (ASDs) called the cortical metric. Absence of such an outcome measure has greatly hindered the development of treatments for core symptoms of ASD.