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NCT ID: NCT01987960 Terminated - PTSD Clinical Trials

Brexpiprazole as an Additional Treatment to Paroxetine or Sertraline in Adult Patients Suffering From Post-traumatic Stress Disorder (PTSD)

Start date: December 2013
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of brexpiprazole as adjunctive treatment to paroxetine or sertraline on PTSD symptoms.

NCT ID: NCT01987882 Recruiting - Cerebral Palsy Clinical Trials

Cerebral Palsy Hip Outcomes Project - International Multi-centre Study

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

The primary purpose of the project is to evaluate the effectiveness of different intervention strategies to prevent or relieve symptoms associated with hip instability in children with severe cerebral palsy, using the validated Caregiver Priorities and Child Health Index of Life with Disabilities (CPCHILD©) questionnaire as the primary outcome measure of health-related quality of life for this population.

NCT ID: NCT01987804 Completed - Vaginal Atrophy Clinical Trials

Dose-relationship of Vaginally Administrated Oxytocin in Postmenopausal Women

OXYPEP002
Start date: January 2012
Phase: Phase 2
Study type: Interventional

Up to 50% of all postmenopausal women, experience vaginal drynes, i.e. vaginal atrophy is a consequence due to the lack of estrogen. In addition, vaginal atrophy is associated with an increased pH, which creates an environment more susceptible to infections . The mucosal epithelium shows signs of severe senile atrophy and cytological examination demonstrate increased number of the basal and parabasal cells and reduced number of superficial cells . Unlike some other menopausal symptoms (for instance hot flushes), vaginal symptoms generally persist or worsen with aging.Oxytocin is a peptide hormone and it is released systemically via the posterior pituitary. The most well known effects of oxytocin are its roles in female reproduction such as facilitation of birth and breast feeding. Oxytocin has also shown to exert positive effects on the proliferation of human vaginal mucosal cells from postmenopausal women, an effect which could be attributed either to the direct stimulation of new cell formation or to an increased production of other growth factors. The primary objective is to investigate the dose relationsship of topical administrated Vagitocin on the vaginal mucosal membrane, measured in the change (%)of superficial cells up to 7 weeks after baseline.

NCT ID: NCT01987778 Completed - Menopause Clinical Trials

Health Effects of Resistance Training on Postmenopausal Women

Start date: November 2013
Phase: N/A
Study type: Interventional

Today's women will live more than a third of their lives after menopause, i.e. with a changed hormonal and metabolic state. Vasomotor symptoms like hot flushes and sweating are reported by about 75% of all women around menopause and may impair well-being, mental state, daily activities and night sleep. Vasomotor symptoms are less prevalent in women who participate in regular physical exercise. It is, however, still uncertain if physical exercise reduces vasomotor symptoms. The purpose of this randomized controlled study is to establish possible beneficial health effects from 15 weeks of supervised resistance training (RT) on postmenopausal women. End-points include effects from RT in postmenopausal women on 1. clinical outcomes (number and severity of vasomotor symptoms, Health-Related quality of Life (HRQoL), Body Mass Index (BMI), abdominal height, muscle strength and mass, browning of fat), 2. diagnostic variables (production of myokines as irisin, immunological markers) and 3. genetic variables (length of telomeres). The control group will be offered resistance training after the intervention period.

NCT ID: NCT01987674 Terminated - Clinical trials for Type 2 Diabetes Mellitus

Pre-meal Protein Drink Improve Glycemic Regulation

PMB/T2D
Start date: January 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate if a pre-meal drink containing proteins can positively influence glycaemic control in patients with type 2 diabetes mellitus. Comparison with a placebo is included.

NCT ID: NCT01987102 Completed - Osteosarcoma Clinical Trials

Investigation of [6R] 5,10-methylenetetrahydrofolate (Arfolitixorin) as Rescue Therapy for Osteosarcoma Patients Treated With HDMTX.

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

An open-label, multicenter, phase I/II clinical trial to identify the [6R] 5,10-methylenetetrahydrofolate (arfolitixorin) dose with most favorable safety prospect and confirmed ability to mitigate high-dose methotrexate induced toxicity during treatment of osteosarcoma patients

NCT ID: NCT01986816 Withdrawn - Obesity Clinical Trials

Return on Investment on Lap Gastric Bypass Regarding Quality of Life

ROI-LGBP
Start date: April 2014
Phase:
Study type: Observational

The purpose of this study is to investigate the cost of treatment and adverse efffects therof corresponds to quality of life improvements and expected wheightloss.

NCT ID: NCT01986257 Completed - Clinical trials for Borderline Personality Disorder

ERGT for Women Engaging in NSSI - an Effectiveness Study

Start date: October 2013
Phase: N/A
Study type: Interventional

The primary aim is to investigate the effectiveness of Emotion Regulation Group Therapy (ERGT) for women who self-harm in ordinary psychiatric outpatient health care.

NCT ID: NCT01985334 Completed - COPD Clinical Trials

Study to Evaluate the Efficacy and Safety of Glycopyrronium or Indacaterol Maleate and Glycopyrronium Bromide Fixed-dose Combination Regarding Symptoms and Health Status in Patients With Moderate COPD Switching From Treatment With Any Standard COPD Regimen

Start date: February 14, 2014
Phase: Phase 4
Study type: Interventional

The main goal of this study is to evaluate the efficacy and safety of glycopyrronium bromide and indacaterol maleate and glycopyrronium bromide fixed dose combination (FDC) in patients with moderate COPD who switch from their current COPD therapy. This study aims to provide data on how non-exacerbating, but still symptomatic patients with moderate COPD switching from their current COPD treatment to glycopyrronium bromide or indacaterol maleate and glycopyrronium bromide FDC maintain or improve their symptoms. Another purpose of this study is to increase awareness and usage of validated COPD symptoms tools and dyspnea questionnaires in order to facilitate clinical assessment and improve early diagnosis of symptomatic patients.

NCT ID: NCT01985074 Active, not recruiting - Clinical trials for The Focus is to Investigate Effect of a Case Management Interventions in Frequent Visitors to Emergency Departments

A Case Management Study Targeted to Reduce Health Care Utilization for Frequent Emergency Department Visitors

Start date: July 2010
Phase: N/A
Study type: Interventional

The aim of the study is to determine whether a nurse-managed telephone-based case-management intervention can reduce healthcare utilization and improve self-assessed health status in frequent emergency department users.