Clinical Trials Logo

Filter by:
NCT ID: NCT00628329 Withdrawn - Asthma Clinical Trials

Vitamin A, Its Receptors and Asthma

Start date: May 2008
Phase: N/A
Study type: Observational

We wish to understand the association of Vitamin A serum levels and Vitamin A receptor number and responsiveness in asthmatics. We believe that Vitamin A receptors may be less prevalent in asthmatics and their responsiveness decreased.

NCT ID: NCT00627991 Withdrawn - Clinical trials for Cerebrovascular Accident

Blood Pressure Lowering in Acute Stroke Trial (BLAST)

Start date: August 2007
Phase: N/A
Study type: Interventional

Patients who are suffering from a stroke often present to the hospital with elevated blood pressure. Elevated blood pressure in the setting of stroke increases the risk of brain swelling or bleeding into the brain. Even so, there has been concern about lowering the blood pressure with medications because the newly injured parts of the brain may not get the blood flow they need, thereby worsening the damage from the initial stroke. We hope to demonstrate that the drug valsartan can be used safely and modestly to lower blood pressure in acute stroke patients, without having a detrimental effect on brain blood flow or neurologic status. Novel MRI techniques to measure brain blood flow will be used in conjunction with clinical scales to demonstrate safety.

NCT ID: NCT00627627 Withdrawn - Breast Cancer Clinical Trials

A Study to Evaluate the Antitumor Activity and Safety of IPI-504 in Patients With Advanced Breast Cancer

Start date: April 2008
Phase: Phase 1/Phase 2
Study type: Interventional

To evaluate the antitumor activity following treatment with IPI-504 in patients with breast cancer.

NCT ID: NCT00627133 Withdrawn - Clinical trials for Seizure, Alcohol Related

Efficacy of Keppra in Acute Alcohol Related Seizure Control--A Pilot Study

Start date: February 2008
Phase: Phase 2
Study type: Interventional

Pilot study to evaluate efficacy of Keppra (levetiracetam) for seizure control in patients with alcohol related seizures.

NCT ID: NCT00625469 Withdrawn - Clinical trials for Pulmonary Arterial Hypertension

Pulmonary Arterial Hypertension Secondary to Idiopathic Pulmonary Fibrosis and Treatment With Bosentan

Start date: October 2007
Phase: Phase 4
Study type: Interventional

Pulmonary Arterial Hypertension (PAH) in the setting of Idiopathic Pulmonary Fibrosis(IPF)is a risk factor for morbidity and mortality in the peri-lung transplant(LT) setting. Currently there is no significant data to support the use of pulmonary vasodilators for PAH in the setting of interstitial lung disease such as IPF. The majority of IPF patients have PAH either at rest or during exercise. The study hypothesis is that bosentan may improve morbidity and mortality in the peri-LT setting in both IPF cohorts with either resting or exercise PAH.

NCT ID: NCT00625079 Withdrawn - Clinical trials for Pulmonary Hypertension

Pulmonary Hypertension Secondary to Idiopathic Pulmonary Fibrosis And Treatment With Sildenafil

Start date: February 2007
Phase: Phase 4
Study type: Interventional

Pulmonary Arterial Hypertension (PAH) in the setting of Idiopathic Pulmonary Fibrosis(IPF)is a risk factor for morbidity and mortality in the peri-lung transplant(LT) setting. Currently there is no significant data to support the use of pulmonary vasodilators for PAH in the setting of interstitial lung disease such as IPF. The majority of IPF patients have PAH either at rest or during exercise. The study hypothesis is that sildenafil may improve morbidity and mortality in the peri-LT setting in both IPF cohorts with either resting or exercise PAH.

NCT ID: NCT00624312 Withdrawn - Cancer Clinical Trials

Procrit Versus Placebo to Determine Efficacy in Pre-Operative Major Surgical Oncology Operations

Start date: February 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of a two-dose regimen of Procrit prior to a major surgical oncology operation.

NCT ID: NCT00623948 Withdrawn - Pressure Ulcers Clinical Trials

Implanted Gluteal Stimulation System for Pressure Sore Prevention

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

This project will evaluate the feasibility of using a fully implanted gluteal stimulation system for the prevention of Pressure ulcers. The specific goal of this study will be a pilot clinical trial of veterans with reduced mobility in order to establish clinical efficacy of a 2-channel bilateral gluteal stimulation system. A two-arm crossover study of wheelchair users with complete SCI will be carried out. All study participants will receive a fully implanted system incorporating implanted IM electrodes and a Micropulse I IPG stimulator (NDI Medical). Group assignments will be determined at enrollment using a modified randomization scheme. A total of 10 subjects will be recruited to the pilot clinical trial.

NCT ID: NCT00623909 Withdrawn - Laser Therapy Clinical Trials

Laser Therapy in the Treatment of Post Thoracotomy Pain; A Pilot Study

Start date: January 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the safety of the AvicennaTM class IV laser for application over the skin of human subjects. In addition, we seek to measure the effectiveness and utility of this class 4 laser therapy in the treatment of post-thoracotomy pain syndrome.

NCT ID: NCT00622921 Withdrawn - PTSD Clinical Trials

Couples-based Behavioral Psychotherapy for Male Patients With Posttraumatic Stress Disorder and Alcohol Dependence

Start date: February 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Purpose: Phase I focus groups with clinicians and patients will gather qualitative data to focus and inform the content of Phase II. In Phase II, 12 weeks of psychotherapy will be offered to evaluate feasibility and potential efficacy of a couples-based, integrated treatment for men with PTSD and alcohol dependence. Hypotheses: We predict that this experimental psychotherapy, Partners Encouraging Abstinence and Coping with Emotions (PEACE), will reduce patient drinking, reduce PTSD symptoms, and improve relationship functioning.