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NCT ID: NCT00160563 Terminated - Asthma Clinical Trials

Prevention of Asthma With Levocetirizine (36 Month Treatment) in Young Children Suffering From Eczema (Atopic Dermatitis) and Sensitized to Grass Pollen and House Dust Mite and Having Completed the Previous EPAAC Trial (NCT00152464)

Start date: June 2004
Phase: Phase 3
Study type: Interventional

Prolongation of the EPAAC™ trial - NCT00152464 (The Early Prevention of Asthma in Atopic Children). 36 months study to evaluate the efficacy and safety of levocetirizine (LCTZ) in preventing the onset of asthma in young atopic children.

NCT ID: NCT00160524 Completed - Crohn's Disease Clinical Trials

A follow-on Safety Study of CDP870 in Subjects With Crohn's Disease (CD) Who Have Completed a 26-week Double Blind Study CDP870-031 [NCT00152490] or CDP870-032 [NCT00152425]

PRECiSE 3
Start date: July 2004
Phase: Phase 3
Study type: Interventional

An open-label follow-on safety study of CDP870 (400 mg every 4 weeks) in patients with Crohn's Disease who have completed a 26-week blinded study (CDP870-031 [NCT00152490] or CDP870-032 [NCT00152425]).

NCT ID: NCT00160212 Completed - Hypertension Clinical Trials

Study to Evaluate the Efficacy and Safety of SLV306 in Subjects With Hypertension

Start date: December 2004
Phase: Phase 2
Study type: Interventional

This study is to compare the efficacy and safety of increasing doses of SLV306 with amlodipine.

NCT ID: NCT00159887 Completed - Clinical trials for Pulmonary Hypertension

Study to Assess the Longterm Safety of Sildenafil Citrate in Patients With Pulmonary Arterial Hypertension

Start date: December 2002
Phase: Phase 3
Study type: Interventional

Open label extension study to the pivotal efficacy study to assess the safety of sildenafil citrate in patients with pulmonary arterial hypertension

NCT ID: NCT00159640 Terminated - Pain Clinical Trials

Placebo Controlled Dose-Response Study Of PD-217,014 In The Treatment Of Postherpetic Neuralgia

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effectiveness of PD-217,014 in the treatment of chronic pain following a shingles infection.

NCT ID: NCT00157183 Completed - Cystic Fibrosis Clinical Trials

Non-invasive Ventilation and Oxygen Therapy in Cystic Fibrosis Patients With Nocturnal Oxygen Desaturation

Start date: March 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether correction of low nighttime oxygen (O2) levels and/ or high carbon dioxide levels in patients with cystic fibrosis improves their quality of life. The treatments being used overnight are (1)O2 (2)pressurised air which assists breathing (non-invasive positive pressure ventilation, NIPPV)

NCT ID: NCT00157170 Completed - HIV Infections Clinical Trials

The Effects of a Supervised Exercise Program on Self Efficacy of People Living With HIV/AIDS.

Start date: September 2002
Phase: N/A
Study type: Interventional

To evaluate the impact of a supervised exercise program (SEP) on self-efficacy,quality of life status and cardiovascular fitness among people with HIV in a 24 week randomised controlled trial.We hypothesised that a combined aerobic and resisted exercise (intervention) would improve these parameters compared to an individual walking program with monthly group forum (control).

NCT ID: NCT00157144 Completed - Clinical trials for Respiratory Insufficiency

Australia and New Zealand Adult Extracorporeal Membrane Oxygenation (ECMO) Audit 2005

Start date: October 2004
Phase: N/A
Study type: Observational

Extracorporeal membrane oxygenation (ECMO) is a means of artificially performing the function of the human lung and/or heart outside the body. Its use is escalating in a wide range of clinical settings in the adult population without evidence or guidelines to support this practice. This study involves a nationwide questionnaire which has two components. The initial pilot survey will attempt to identify all institutions currently practicing ECMO or those intending to do so in the future, and are willing to participate in prospective data collection. The second phase will involve a monthly survey of these centres regarding the extent of ECMO use, practice details implemented, and outcome data. It is hoped that the collection of this information will later assist in the development of guidelines for this expensive and presently unsubstantiated practice, together with the construction of appropriate training programs for staff.

NCT ID: NCT00156325 Completed - Bipolar Disorders Clinical Trials

Escitalopram as a Mood Stabilizer for Bipolar II Disorder

Start date: February 2004
Phase: Phase 2
Study type: Interventional

This study will investigate the efficacy of Escitalopram, a Selective Serotonin Reuptake Inhibitor (SSRI) antidepressant, in the treatment of Bipolar II Disorder. The use of antidepressants for those with bipolar disorder appears common in clinical practice but is not countenanced - at least as monotherapy - in formal treatment guidelines. This view reflects concerns about the possibility of antidepressant drugs inducing switching and rapid cycling in those with Bipolar Disorder. Although the effectiveness of treating Bipolar II patients with SSRIs has received very little attention in the literature, observations of Bipolar II patients treated with SSRIs suggest they may have general mood stabilising properties. Many patients have reported improvements not only in their depressed mood, but also a reduction in the severity, duration and frequency of hypomanic episodes. In this proof of concept study we specifically assess whether a standard dose of an SSRI antidepressant is more effective than placebo in reducing the frequency, severity and duration of both depressive and hypomanic episodes.

NCT ID: NCT00155987 Completed - Brain Injuries Clinical Trials

The DECRA Trial: Early Decompressive Craniectomy in Patients With Severe Traumatic Brain Injury

Start date: August 2003
Phase: Phase 3
Study type: Interventional

This is a multi-centre randomised trial to evaluate the effect of early decompressive craniectomy on neurological function in patients with severe traumatic brain injury. The primary outcome is neurological function measured at 6 months post injury using the Glasgow Outcome Score. Neurological function is qualified as proportion of favourable outcomes (Glasgow Outcome Score Extended [GOSE] grades 5-8).