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NCT ID: NCT00733252 Withdrawn - Lung Cancer Clinical Trials

Optical Coherence Tomography of the Airway for Lung Cancer or Lung Disease

Start date: April 2008
Phase: Phase 1
Study type: Observational

RATIONALE: Diagnostic procedures, such as optical coherence tomography, may help find and diagnose lung cancer or precancerous cells. PURPOSE: This phase I trial is studying how well optical coherence tomography of the airway works in detecting abnormal cells in patients undergoing surgery for lung cancer or lung disease.

NCT ID: NCT00732186 Withdrawn - Clinical trials for Leukemia, Myeloid, Chronic

Study of Ipilimumab and Dasatinib Combination Therapy in Patients With Chronic or Accelerated Chronic Myeloid Leukemia

Start date: August 2009
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the safety of ipilimumab and dasatinib combination therapy in patients with CML

NCT ID: NCT00732108 Withdrawn - Migraine Clinical Trials

Is Topiramate Effective in Treating Dizziness in Patient's With Migraine-Associated Dizziness

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

The purpose of this study is to determine whether topiramate effective in treating dizziness symptoms that are associated with migraine headaches.

NCT ID: NCT00731757 Withdrawn - Sarcoidosis Clinical Trials

Efficacy Study of Humira in the Treatment of Cutaneous Sarcoidosis

Start date: May 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of Humira in the treatment of cutaneous sarcoidosis.

NCT ID: NCT00730717 Withdrawn - Clinical trials for Pyoderma Gangrenosum

Safety and Efficacy Study of Humira in Treatment of Pyoderma Gangrenosum

Start date: May 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of Humira in the treatment of pyoderma gangrenosum.

NCT ID: NCT00730587 Withdrawn - Healthy Clinical Trials

Study of Body Composition Methodology in Young Children (InfantPod)

Start date: n/a
Phase: N/A
Study type: Observational

The InfantPod study is a cross-sectional study designed to determine how practical and precise a body composition method is for measuring body fat and lean tissue in infants and children ages 5 months to 3 years.

NCT ID: NCT00730119 Withdrawn - Respiration Clinical Trials

Evaluation Of The GE Monitor Product Line

Start date: October 2001
Phase: N/A
Study type: Observational

This investigation is a multi-center study that will demonstrate that the GE Monitor meets equivalency and/or accuracy and/or performance criteria. This investigation will compare the test device(s) to itself, or one of the reference parameters, or a combination of parameters, including NIBP, temperature, SpO2, respirations, and ECG.

NCT ID: NCT00728104 Withdrawn - Clinical trials for Cyclic Vomiting Syndrome

The Use of L-Carnitine And CoQ10 Supplements In the Treatment of Cyclic Vomiting Syndrome (CVS)

Start date: October 2007
Phase: N/A
Study type: Observational

This is a study with the principle goal being to learn about the use of L-Carnitine and CoQ10, two vitamin supplements that are currently being used to treat Cyclic Vomiting Syndrome, largely initiated by parents. We want to learn how effective these supplements are compared to standard treatment, at what dose, and what onset of action in order to initiate future prospective study on these supplements.

NCT ID: NCT00728000 Withdrawn - Clinical trials for Pancreatic Adenocarcinoma

Phase II Study Of Neoadjuvant Chemotherapy In Borderline Resectable Pancreatic Adenocarcinoma

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

The goal of this study is to determine the effect of chemotherapy on decreasing the size of unresectable pancreas cancer thereby allowing it to be surgically removed. In addition, this study may provide information on how tumors behave when exposed to certain types of chemotherapy.

NCT ID: NCT00727051 Withdrawn - Clinical trials for Coronary Artery Disease

Comparison of Coronary CT Angiography With Conventional Coronary Angiography in Liver and Lung Transplant Candidates

Start date: June 2007
Phase:
Study type: Observational

The overall goal of this study is to determine if non-invasive imaging with state of the art CT coronary angiography can be used to screen for coronary artery disease in high risk patients prior to liver and lung transplantation. The current protocol for coronary artery disease assessment at UCSF before liver and lung transplantation involves screening with stress tests and/or coronary angiograms in patients with increased risk of coronary artery disease. Coronary angiogram will be used as gold standard for assessment of coronary CTA accuracy.