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NCT ID: NCT01613820 Withdrawn - Clinical trials for Major Depressive Disorder

Ketamine and Scopolamine Infusions for Treatment-resistant Major Depressive Disorder

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

Ketamine infusions resulted in an acute reduction in global depression scores and in severity of suicidal ideation. Scopolamine infusions produced also a significant improvement in depression that was sustained over time. We therefore plan to investigate the feasibility and efficacy of open-label repeated intravenous administration of ketamine and scopolamine combined in this population of severely depressed, treatment-resistant patients. The results from this study could lead to the development of new strategies for the treatment of patients with TRD.

NCT ID: NCT01612104 Completed - Clinical trials for Post Traumatic Stress Disorder

Psychological First Aid With Children in a High Risk Group - a Repeated Single Case Design

Start date: March 2012
Phase: Phase 1
Study type: Interventional

The purpose of this pilot-study is to evaluate a cognitive behavioral method "Psychological First Aid" used with a group of children (11-16 years) in high risk of developing psychological problems. Participants are recruited from a low-threshold program ("The Children's House in Oslo") where counseling is given to children suspected of being physically or sexually abused, or having witnessed domestic violence. The study includes twelve children and teenagers that receive 2 to 6 sessions of counseling. Psychological problems (e.g. anxiety, depression, reactions to trauma) and quality of life will be assessed at pre- post and follow-up (after 3, 6 and 12 months). In addition, some symptoms of will be assessed daily.

NCT ID: NCT01608399 Completed - Clinical trials for Major Depressive Disorder

Clinical Trial of the Effectiveness of Metacognitive Therapy in the Treatment of Patients With Major Depressive Disorder

Start date: March 2012
Phase: N/A
Study type: Interventional

The main aim of this study is to (1) evaluate the effectiveness of metacognitive therapy for major depressive disorder. Additional aims are to (2) investigate patterns of change and the mechanisms of action involved during treatment, and to (3) examine the impact of meta-cognitions in the treatment and relapse prevention of depression.

NCT ID: NCT01607658 Completed - Clinical trials for Female Orgasmic Disorder

Efficacy and Safety of TBS-2 Testosterone Gel in Women With Acquired Female Orgasmic Disorder

Start date: May 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess and compare the effects of 3 dose strengths of TBS-2 intranasal testosterone gel to placebo on the occurrence of orgasm.

NCT ID: NCT01607593 Completed - Clinical trials for Posttraumatic Stress Disorder

A Retrospective And Multicenter Survey To Investigate The Dosage, Efficacy And Safety Of Sertraline In Posttraumatic Stress Disorder Patients

Start date: August 2012
Phase:
Study type: Observational

This is a multicenter retrospective study to investigate the dosage regimens of sertraline in the treatment of Posttraumatic Stress Disorder (PTSD) under current medical practice and the efficacy and safety of this drug in patients with PTSD. Data will be collected from the medical records of patients with PTSD.

NCT ID: NCT01604161 Completed - Turner Syndrome Clinical Trials

Non-interventional Study of Patients Using Norditropin® for Growth Hormone Deficiency or Turner Syndrome

NordiPAD
Start date: May 2005
Phase: N/A
Study type: Observational

This study is conducted in Japan. The aim of this study is to collect information about the efficacy and safety of Norditropin® (somatropin) in the long-term treatment of short stature with GHD (Growth Hormone Deficiency) where epiphysial discs are not closed and short stature with Turner Syndrome where epiphysial discs are not closed.

NCT ID: NCT01602029 Completed - Schizophrenia Clinical Trials

Randomized Double Blind Placebo Control Study in Patients With Schizophrenia

ROSES
Start date: August 2010
Phase: Phase 2
Study type: Interventional

Negative symptoms and cognitive deficits are two partially-related features of schizophrenia which have a major negative impact on social function and objective quality of life. Standard drug treatments have little impact on either and arguably no effect on primary negative symptoms. Social dysfunction has major economic consequences in both the developed and developing world. There is evidence that anti-inflammatory treatment may have beneficial effects in patients with schizophrenia.

NCT ID: NCT01602016 Terminated - Clinical trials for Autism Spectrum Disorder

A Folinic Acid Intervention for Autism Spectrum Disorders

Start date: May 2012
Phase: Phase 2
Study type: Interventional

Researchers at Arkansas Children's Hospital Research Institute are conducting a study looking at the effects of Folinic Acid on language in Autism Spectrum Disorder and language impairment. The study has 3 phases. Phase 1 confirms that your child has language impairment (there is no compensation for this visit). If language impairment is verified in the phase 1 screening, then your child will be eligible for phase 2. Phase 2 consists of receiving 12 weeks of folinic acid or an inactive placebo, in addition to several evaluations of your child's abilities and a single blood test. Children that complete phase 2 will be eligible for a 12 week open-label trial of folinic acid which is phase 3.

NCT ID: NCT01601340 Terminated - Sickle Cell Disease Clinical Trials

Effects of HQK-1001 in Patients With Sickle Cell Disease

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of HQK-1001 on Hb F in subjects with sickle cell disease.

NCT ID: NCT01601210 Completed - Clinical trials for Major Depressive Disorder

Dose-Ranging Trial of Creatine Augmentation for Adolescent Females With Treatment-Resistant Major Depressive Disorder

Start date: June 2012
Phase: Phase 0
Study type: Interventional

The purpose of this study is to see if creatine, which is a naturally occurring chemical in the body, is effective for treating Major Depressive Disorder (MDD) in female teenagers. The primary hypothesis is that compared to placebo, 2g, 4g, and 10g of creatine monohydrate for eight weeks will be associated with a significant increase in brain phosphocreatine (PCr) concentrations.