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NCT ID: NCT01126853 Withdrawn - Hepatitis B Clinical Trials

Combination Hepatitis A and B Vaccine to Induce Immunity in Non-responders

Start date: April 2010
Phase: Phase 4
Study type: Interventional

Hepatitis B is a vaccine preventable infection which can be transmitted through occupational exposure. Approximately 15% of patients will not respond to an initial series of vaccination. Of those re-vaccinated approximately fifty percent will respond. On the basis of poor response to a third series, repeat vaccination is not recommended and non-responders are considered vulnerable to infection. Cardell studied the use of double dose combination hepatitis A and B vaccine (Twinrix) in non responders who had received four or more doses previously and found a high response rate suggesting this vaccine and dose could be effective. The investigators study seeks to duplicate the findings of Cardell, using a more strict definition of non-responder (6 or more previous doses).

NCT ID: NCT01135199 Withdrawn - Pulmonary Fibrosis Clinical Trials

Pomalidomide for Cough in Patients With Idiopathic Pulmonary Fibrosis

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of pomalidomide over a 12 week duration in the treatment of chronic cough in patients with IPF as measured by a Cough Symptom Diary, Visual Analogue Scale for Cough Severity, Leicester Cough Questionnaire, St. George Respiratory Questionnaire, Cough-Specific Quality-of-Life Questionnaire, and adverse event reporting. There will be an option open to participants, who respond to treatment by meeting pre-determined criteria, to remain in the study for an additional 9 months or for a total of 54 weeks.

NCT ID: NCT01152658 Withdrawn - Clinical trials for Partial Supraspinatus Tear

Partial Tear of Supraspinatus (SSP) and Treatment With Plasma Rich in Growth Factors (PRGF)

PrgfRC001IL
Start date: April 2010
Phase: Phase 1
Study type: Interventional

The objective of this clinical trial is to evaluate the impact and symptomatic efficacy of platelets rich plasma (PRP \ PRGF) in the treatment of partial tears of supraspinatus tendon of rotator cuff. Speed of tendon healing of partial thickness tear of the supraspinatus tendon influenced by local injection of platelets rich plasma

NCT ID: NCT01154504 Withdrawn - Heart Failure Clinical Trials

The Role of Adrenomedullin on the Outcome of Severe Heart Failure: a Clinical Randomized Study

Start date: April 2010
Phase: N/A
Study type: Interventional

1. Study Hypothesis: - The decrease of plasma adrenomedullin (ADM) concentration by ultrafiltration and isovolumetric hemofiltration in patients with acute III and IV Class New York Heart Association Functional(NYHA) heart failure is more pronounced than a standard diuretic treatment and is related with clinical improvement. 2. Outcome Measurements: To correlate the adrenomedullin plasma levels with clinical treatment, ultrafiltration and hemofiltration related to: - Brain natriuretic peptide (BNP) level - angiotensin II level - sympathetic nervous activity - oxydative stress - clinical outcome at the beginning, at discharge and 90 days after randomization.

NCT ID: NCT01171456 Withdrawn - Clinical trials for Gestational Diabetes Mellitus

Early Intervention for Gestational Diabetes

Start date: April 2010
Phase: N/A
Study type: Interventional

Gestational diabetes (GDM) represents a significant and growing source nationwide of morbidity and mortality for both mothers and infants. Between 5 and 10% of pregnancies are complicated by GDM. Infants exposed in utero to hyperglycemia from GDM have an increased risk of neonatal complications as well as an increased prevalence of a number of chronic diseases, including type 2 diabetes and schizophrenia. Recent research shows that treatment with metformin begun as soon as hyperglycemia is detected in pregnancy is safe and effective. Additional studies demonstrated that metformin is able to decrease the incidence of type 2 diabetes among individuals at risk for this disease. Based upon these findings, the investigators propose to test the hypothesis that metformin therapy for women at risk for gestational diabetes, started prior to conception and before the onset of hyperglycemia, both decreases the incidence of and improves the maternal and neonatal outcomes from GDM. The investigators intend to conduct a prospective, randomized, double-blind placebo controlled range-finding study to measure the effects of early metabolic intervention with metformin in women at risk for GDM before the commencement of pregnancy or prior to completion of the first trimester. The target sample size for this pilot study is 100 women. The effect size observed will provide preliminary data for a subsequent study which will be sufficiently powered to detect small or moderate effects from early metabolic intervention in women at risk for GDM. The specific aims of the proposed research consist of the following: 1. Determine whether treating women at risk for GDM with metformin prior to conception and/or completion of the 1st trimester decreases the incidence of GDM at 26 weeks' gestation. 2. Evaluate the effects on maternal and fetal pregnancy outcomes of pre-conception metabolic intervention with metformin in women at risk for GDM. 3. Use these pilot study results to: 1. identify specific demographic characteristics associated with an intervention effect 2. calculate effect size for specific outcomes 3. provide range-finding data for a subsequent study design Metformin therapy for women at risk for gestational diabetes, started prior to conception and before the onset of hyperglycemia, both decreases the incidence of and improves the maternal and neonatal outcomes from GDM.

NCT ID: NCT01219530 Withdrawn - Psychopathology Clinical Trials

Follow Up of Gestational Carriers and Intended Parents

Start date: April 2010
Phase: N/A
Study type: Observational

To explore the attitudes and reactions of gestational carriers and intended parents though their medical, pregnancy and postpartum experiences.

NCT ID: NCT01302717 Withdrawn - Sick Sinus Syndrome Clinical Trials

Left Ventricular Pacing to Avoid Cardiac Enlargement Study

LVPACE
Start date: April 2010
Phase: N/A
Study type: Interventional

In this study, the investigators will examine whether left ventricular pacing is superior to right ventricular apical pacing in preventing deterioration of left ventricular systolic function and cardiac remodeling in patients with bradycardia with high risk for development of pacing-induced heart failure.

NCT ID: NCT01381640 Withdrawn - Healthy Subjects Clinical Trials

A Study to Compare Two Paracetamol Tablets

Start date: April 2010
Phase: Phase 1
Study type: Interventional

This is a single dose pharmacoscintigraphic study investigating the differences in paracetamol absorption between two formulations.

NCT ID: NCT01389674 Withdrawn - Angina Pectoris Clinical Trials

Hybrid Intraprocedural Imaging Based on 2 Different Imaging Methods

Start date: April 2010
Phase: N/A
Study type: Interventional

The investigators will check the feasibility of an intraprocedural vitality diagnostics and the identification of an indication for Percutaneous transluminal coronary angioplasty (PTCA).

NCT ID: NCT01556334 Withdrawn - Clinical trials for Preterm Premature Ruptured Membranes

Erythromycin Versus Azithromycin in Preterm Premature Rupture of Membranes

PEACE
Start date: April 2010
Phase: Phase 3
Study type: Interventional

Preterm Premature Rupture of Membranes (PPROM) is treated with an antibiotic, erythromycin or azithromycin, to prolong pregnancy. Erythromycin is taken for several days and can result in stomach upset in some patients, causing them to stop taking the medication. Therefore, azithromycin is often prescribed instead. Azithromycin is usually taken only once and stomach upset is not seen or greatly reduced. The goal of this study is to see if there is a difference between the antibiotic (azithromycin) compared to the antibiotic (erythromycin) in prolonging pregnancy in patients with Preterm Premature Rupture of Membranes (PPROM). The working hypothesis is that there is no difference in the clinical effectiveness between antibiotic regimens containing the macrolides azithromycin and erythromycin for prolonging latency in PPROM.