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NCT ID: NCT00388492 Not yet recruiting - HIV Infections Clinical Trials

BLADE: Comparison of Once Daily Lopinavir/Ritonavir to Lopinavir/Ritonavir BID Dosing in HIV-Infected Subjects

Start date: n/a
Phase: Phase 4
Study type: Observational

The goal of this study is to evaluate the proportion of subjects both antiretroviral experienced and virologically suppressed on lopinavir/ritonavir (LPV/r)400/100mg twice daily who maintain viral suppression after switching to lopinavir/ritonavir (LPV/r)800/200mg once daily. The hypothesis for this study is that the majority of subjects will remain virologically suppressed with once daily dosing versus twice daily dosing and therefore quality of life will be improved with the once daily dosing of lopinavir/ritonavir (LPV/r)800/200mg.

NCT ID: NCT00343954 Not yet recruiting - Sickle Cell Disease Clinical Trials

PK and PD Responses to Oral L-Citrulline in Patients With Sickle Cell Disease

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

To evaluate PK and PD responses to L-citrulline given orally for four weeks to patients with sickle cell disease who are otherwise healthy.

NCT ID: NCT00318513 Not yet recruiting - Lymphedema Clinical Trials

Safety Study of Bevacizumab to Treat Women With a History of Breast Cancer and Suffering From Upper Extremity Lymphedema

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

The purpose of this study is to determine the safety and side effects of bevacizumab in subjects with lymphedema who will initially receive bevacizumab alone and then in combination with standard manual lymphatic drainage (MLD) and combined decongestive therapy (CDT). This study will help to determine the dose of bevacizumab to be used in future studies of subjects with lymphedema.

NCT ID: NCT00294242 Not yet recruiting - Pregnancy Clinical Trials

Safety Study of Membrane Sweeping in Pregnancy

Start date: February 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if routine membrane sweeping in uncomplicated term pregnancies increases the rate of pre-labor rupture of membranes.

NCT ID: NCT00286923 Not yet recruiting - Migraine Clinical Trials

Does Topiramate Adjust the Excitability of the Brain in Migraine Sufferers?

Start date: February 2006
Phase: N/A
Study type: Observational

The purpose of the study is to determine by the use of non-invasive magnetic stimulation if the medication Topiramate adjusts the excitability of the migraine sufferer's brain. Previous studies have shown the migraine sufferer's brain is more excitable. The magnetic stimulation device has given us a way to look at excitability and to see if it changes at the same time that a headache diary shows if the pattern or severity of headaches changes with the administration of the drug Topiramate. It is expected that as migraine sufferers have fewer headaches with topiramate the testing with magnetic stimulation will show that their brains are less excitable and that if the topiramate does not change the character of headaches then the pattern of excitabilty would not change from the baseline test before medication is started.

NCT ID: NCT00269139 Not yet recruiting - Clinical trials for Borderline Personality Disorder

Outcome of Crisis Intervention for Subjects With Borderline Personality Disorder or Post-Traumatic Stress Disorder

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

Dr. Laddis will test a hypothesis about the nature and the management of behavioral crises in patients with borderline personality disorder (BPD) or post-traumatic stress disorder (PTSD). The term "behavioral crisis" is used strictly for periods of uncontrollable urges to repeat mental or outward activity, e.g., flashbacks, cutting, binging on food, drugs or sex, with no intervals to rethink one's priorities or to consider others' direction. The clinical hypothesis states, in two steps, that: 1. the perception of a life crisis precedes and then underlies every behavioral crisis; 2. the behavioral crisis resolves promptly and all symptoms end if the clinicians engage the patient about his management of the life crisis that underlies the symptoms.

NCT ID: NCT00261144 Not yet recruiting - Cellulite Clinical Trials

Collagenase in the Treatment of Cellulite

Start date: February 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if collagenase injection will reduce or eliminate the appearance of cellulite of the thigh.

NCT ID: NCT00260767 Not yet recruiting - HIV Clinical Trials

Imaging Trial of the Distribution of Topical Gel in the Human Vagina: Enhanced MRI Techniques to Increase Resolution

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

This study will assess the distribution of topical gel in the human vagina, using enhanced MRI techniques. The number and size of uncovered areas will be studied, and the upper genital tract will be examined for the presence of topical gel using MRI.

NCT ID: NCT00253279 Not yet recruiting - Burn Clinical Trials

Alterations in Protein Synthesis Rates of Burn Patients Measured Over Time Using PET Scans

Start date: November 2009
Phase: Phase 1
Study type: Observational

Our specific aim is to gain an understanding of protein synthesis rates in burn patients at various times during their injury and recovery by using PET scans. This will be compared with healthy volunteer controls. We hope this will help optimize nutrition and care regimens for future burn patients.

NCT ID: NCT00238849 Not yet recruiting - Clinical trials for Previously Treated Metastatic Non-Small Cell Lung Cancer

Phase II Study of Oxaliplatin and Navelbine for Second-Line Treatment of Advanced NSCLC.

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the response rate to treatment with oxaliplatin and Navelbine in patients with previously treated NSCLC. Oxaliplatin and Navelbine have not been clinically evaluated yet. However, Navelbine has been safely administered with other platinum compounds.