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NCT ID: NCT01755728 Completed - PDA Clinical Trials

Paracetamol (Acetaminophen) for Closure of PDA in Preterm Infants

Start date: January 1, 2013
Phase: Phase 3
Study type: Interventional

There is a report that acetaminophen may have a role in pharmacological closure of PDA (Patent arterial duct) in preterm infants. The investigators conducted this open label non randomized and non control study to try to support that report.

NCT ID: NCT01754948 Recruiting - Asthma Clinical Trials

Biological Monitoring of Nano Sized Particles in the Airways of Asthmatic Children

EHF
Start date: July 2012
Phase: N/A
Study type: Observational

Background Ambient airborne particulate material (PM) is defined according the aerodynamic diameter into coarse, fine, and ultrafine or "nano" sized particles ranging between 2.5-10 µm (coarse), <2.5 µm (fine), and <0.1 µm (nano(. Many studies have examined particle effect on respiratory health in children, mainly by environmental monitoring of coarse and fine particles. Biological assessment of individual exposure to nano sized particles in correlation to adverse health effect was not previously studied. Hypothesis individual exposure to nano sized particles in children is associated with reduction in forced expiratory volume at one second.

NCT ID: NCT01754532 Completed - Schizophrenia Clinical Trials

Correlation Between Clinical Deterioration in Schizophrenic Patients and Hair Cortisol Levels

Start date: January 2013
Phase:
Study type: Observational

The importance of stress as a possible deteriorating factor for schizophrenic patients is well documented. However, this notion is based on subjective experience and retrospective psychological analysis. A novel method of measuring cortisol using hair has a proven correlation to subjective stress in non-clinical as well as psychiatric clinical populations. This pilot study will attempt to assess the use of cortisol hair level, as a marker of stress, to predict clinical deterioration in schizophrenic patients.

NCT ID: NCT01753960 Not yet recruiting - Hemorrhage Clinical Trials

Surgical Blood Management Using Noninvasive and Continuous Hemoglobin Monitoring(NACHO)

Start date: January 2013
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether Noninvasive and Continuous Hemoglobin Monitoring (NACHO) for Surgical Blood Management affects transfusion decision making algorithm in the operating room.

NCT ID: NCT01753817 Not yet recruiting - Clinical trials for Coronary Catheterization

Assessment of Radial Artery Patency Following Catheterization With a 7F Sheath

Start date: January 2013
Phase: N/A
Study type: Observational

Radial artery occlusion may occur after performance of coronary catheterization via the radial artery (transradial approach). In some cases it may be desirable to insert large (7F) catheters via the radial artery, however the impact of increased catheter size on subsequent radial artery patency is unclear. We hypothesize that radial artery occlusion following 7F catheterization is rare and occurs in < 5% of the cases.

NCT ID: NCT01753609 Not yet recruiting - Obesity Clinical Trials

Safety and Performance Evaluation of Tulip Device in Healthy Overweight and Obese Volunteers

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

The study will assess the safety and performance of an intragastric auto-inflating and degradable balloon

NCT ID: NCT01753349 Completed - Cervical Dystonia Clinical Trials

Phase IV-Cervical Dystonia-INTEREST IN CD2

INTEREST_INCD2
Start date: December 2012
Phase:
Study type: Observational

The purpose of the study is to document long-term response in real-life practice after injection cycles with BoNT-A in subjects suffering from idiopathic cervical dystonia (Long-term clinical and pharmaco-economic data).

NCT ID: NCT01753258 Completed - Pregnancy Clinical Trials

Outcomes of Delivery in Patients With Dyspareunia

Start date: January 2013
Phase: N/A
Study type: Observational

The focus of this pilot study is to determine if a woman who experiences pain during sexual intercourse has a higher risk of complications during labor and delivery secondary to pelvic floor dysfunction, anxiety and intolerance towards pelvic examinations. Furthermore, it is unclear whether women with prepartum dyspareunia experience an improvement following vaginal delivery. While physicians may expect that vaginal birth improves dyspareunia due to the stretching effect on pelvic floor, to date, there is insufficient evidence to support this claim. The Investigators plan to prospectively study 200 patients at our Institution, collect information regarding birth and follow them, via questionnaires, regarding their dyspareunia postpartum.

NCT ID: NCT01753180 Completed - Clinical trials for Chronic Coronary Total Occlusions

Total Occlusion Study in Coronary Arteries - 5

TOSCA-5
Start date: April 2014
Phase: Phase 2
Study type: Interventional

A prospective, multi-center, double blind, 2 stage, placebo-controlled, phase II study, evaluating acute intra-coronary injected collagenase prior to routine standard-of-care percutaneous revascularization procedures in subjects with chronic total coronary artery occlusions (CTOs).

NCT ID: NCT01751126 Completed - Clinical trials for Vernal Keratoconjunctivitis

Double-Masked Trial of NOVA22007 (1mg/mL Ciclosporin/Cyclosporine) Versus Vehicle in Pediatric Patients With Active Severe Vernal Keratoconjunctivitis

Start date: April 29, 2013
Phase: Phase 3
Study type: Interventional

The objective of this study is to compare the efficacy of two different dosing regimen of NOVA22007 (1mg/ml ciclosporin/cyclosporine) eye drops, emulsion versus placebo (vehicle of the formulation) administered four times a day in patients with severe vernal keratoconjunctivitis after 4 months of treatment.