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NCT ID: NCT00501189 Withdrawn - Clinical trials for Papillomavirus Infections

Gardasil Vaccination as Therapy in Low Grade Cervical Abnormalities

Start date: August 2007
Phase:
Study type: Observational

This project will compare the rate of regression of minimally abnormal Pap smears to normal in women who receive Gardasil to a historical control group. Research hypothesis: Women with low grade cervical dysplasia on Papanicolaou (Pap) smear that receive Gardasil vaccination will revert to a normal within one year at a rate 33% higher than historical controls that did not receive Gardasil vaccination.

NCT ID: NCT00497640 Withdrawn - Clinical trials for Obstructive Sleep Apnea

CPAP Titration Using an Artificial Neural Network: A Randomized Controlled Study

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

The purpose of the study is to determine the validity of the prediction model in reducing the rate of CPAP titration failure and in achieving a shorter time to optimal pressure

NCT ID: NCT00494156 Withdrawn - Clinical trials for Vertebral Artery Injury

Anticoagulation in Blunt Cerebrovascular Injuries

Start date: July 2003
Phase: N/A
Study type: Interventional

Originally thought to be a rare occurrence, BCVI are now diagnosed in approximately 1% of blunt trauma patients. Initially BCVI were thought to have unavoidable devastating neurologic outcomes. But early reports suggested anticoagulation might decrease these events. If untreated, carotid artery injuries (CAI) have a stoke rate up to 50% depending on injury grade, with increasing stroke rates correlating with increasing grades of injury. Current studies report early treatment with antithrombotics - either heparin or anti-platelet agents - in patients with BCVI markedly reduces stroke rates and resultant neurologic morbidity. As reports of bleeding complications have altered heparin protocols in these patients, the use of antiplatelet agents is attractive. Although heparin has been has been proposed as the gold standard treatment due to its initial empiric use, no comparative studies of antithrombotic agents has been performed. In sum, Grade I-III blunt carotid and vertebral arterial injuries (BCVI) have the potential for stroke, and should be treated. Heparin has not been shown to clearly improve healing rates compared with antiplatelet therapy. The purpose of this study is to determine whether systemic anticoagulation alters the course of Grade I-III BCVI compared with antiplatelet therapy. The investigators study hypothesis is that Grade I-III BCVI will heal or progress to pseudoaneurysm formation, independent of systemic antithrombotic regimen, and that the combination of aspirin and clopidogrel is equally efficacious in preventing neurologic symptoms compared to systemic heparin associated with Grade I-III BCVI.

NCT ID: NCT00492947 Withdrawn - Clinical trials for Squamous Cell Carcinoma of Head and Neck

Dendritic Cell Vaccine for Head and Neck Cancer

Dendritic
Start date: June 2007
Phase: Phase 1
Study type: Interventional

This research study is testing a new treatment of cancer of the head and neck. Purpose This research study is being done to: 1. Test the safety of the experimental cancer vaccine made of dendritic cells. An experimental vaccine is one that is not approved by the Food and Drug Administration (FDA). 2. To learn what effects (good and bad) the vaccine will have on you and your head and neck cancer. 3. To learn if the vaccine will stimulate your body's white blood cells, which are part of your immune system (your body's natural defense system).

NCT ID: NCT00488605 Withdrawn - Leukemia Clinical Trials

H-9926-LCH III: Treatment Protocol of the Third International Study for Langerhans Cell Histiocytosis

Start date: August 1, 2023
Phase: Phase 3
Study type: Interventional

LCH III is an international, multicentric, prospective clinical study comprised of: - a randomized clinical trial for multisystem "RISK" patients and - a randomized clinical trial for multisystem "LOW RISK" patients and - a pilot study for patients with single system MFB and localized "SPECIAL SITES"

NCT ID: NCT00487799 Withdrawn - Clinical trials for Heart Failure, Congestive

A Study of Ularitide in the Treatment of Subjects With Acute Decompensated Heart Failure

Start date: n/a
Phase: Phase 1
Study type: Interventional

To determine the maximum tolerated dose (MTD) of ularitide in the treatment of subjects hospitalized with symptomatic acute decompensated heart failure (ADHF).

NCT ID: NCT00485966 Withdrawn - Clinical trials for B-Cell Chronic Lymphocytic Leukemia

Study Evaluating Effects of CX-3543 in Patients With Relapsed or Refractory B-Cell Chronic Lymphocytic Leukemia

Start date: June 2007
Phase: Phase 2
Study type: Interventional

This is a Phase 2, open-label, multicenter, efficacy, safety, and pharmacodynamic study of CX-3543 in patients with relapsed or refractory B-cell chronic lymphocytic leukemia (CLL).

NCT ID: NCT00484666 Withdrawn - Ovarian Cancer Clinical Trials

Platinum-Resistant, Recurrent Epithelial Ovarian Cancer

TopoTxt
Start date: May 2006
Phase:
Study type: Observational

Primary objective: To estimate the overall clinical response rate (CR, PR, SD) of weekly docetaxel and weekly topotecan in women with recurrent platinum resistant ovarian or primary peritoneal cancer. Secondary objectives: To access the safety and tolerability of this novel combination chemotherapy regimen of weekly docetaxel and weekly topotecan in women with recurrent platinum resistant ovarian or primary peritoneal cancer To estimate the progression free survival (PFS) and overall survival (OS) for women with recurrent platinum resistant ovarian or primary peritoneal cancer treated with this weekly docetaxel and weekly topotecan.

NCT ID: NCT00484172 Withdrawn - Obesity Clinical Trials

Genomic Search for Childhood Obesity Genes-A Pilot Study

Start date: June 2007
Phase:
Study type: Observational

The purpose of this study is to screen a pediatric population (ages 2-8) for genes associated with childhood obesity.

NCT ID: NCT00483600 Withdrawn - Kidney Diseases Clinical Trials

Pharmacokinetic Study of Fondaparinux in Outpatients With Renal Dysfunction

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

To determine the appropriate dose and safety of a preventative dose of fondaparinux, an anticoagulant medication (blood thinner) in patients with kidney disease.