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NCT ID: NCT01356485 Completed - Sickle Cell Disease Clinical Trials

Safety Study of MP4CO in Adult Sickle Cell Patients

Start date: January 2012
Phase: Phase 1
Study type: Interventional

Sickle Cell Anemia is caused by an inherited hemoglobin disorder. Healthy red blood cells are discoid and can deform and move through small blood vessels to carry oxygen to all parts of the body. In sickle cell disease, as red blood cells circulate and oxygen is released in the circulatory system, the deoxygenated abnormal hemoglobin S can begin to polymerize. When this occurs, the red blood cells can become sticky and elongated. These sickled red blood cells are less flexible and will obstruct small blood vessels and block normal red blood cells from traveling through the circulatory system, which limits oxygen delivery to tissues and organs. This is known as a "sickle crisis". Patients suffering from a sickle crisis experience severe pain and are at risk of stroke, heart attack or even death. By lowering the level of oxygen pressure at which sickling occurs and opening the vasculature and rapidly delivering oxygen directly to ischemic tissues, the addition of MP4CO to existing treatment protocols may alleviate pain associated with a sickle cell crisis, abort a crisis and/or potentially reduce the duration of a crisis. This could mean less time in the hospital and an improved quality of life for patients with sickle cell anemia.

NCT ID: NCT01355159 Completed - Preeclampsia Clinical Trials

High Dose Folic Acid Supplementation Throughout Pregnancy for Preeclampsia Prevention

FACT
Start date: April 2011
Phase: Phase 3
Study type: Interventional

To determine the efficacy of high dose folic acid supplementation for prevention of preeclampsia in women with at least one risk factor: pre-existing hypertension, pre-pregnancy diabetes (type 1 or 2), twin pregnancy, preeclampsia in a previous pregnancy, or body mass index ≥35. It was hypothesized that high dose (4.0 mg per day) supplementation starting in early pregnancy and continued throughout the entire pregnancy will lower the incidence of preeclampsia in pregnant women at high risk of developing preeclampsia.

NCT ID: NCT01322269 Completed - Sickle Cell Disease Clinical Trials

A Study of HQK-1001 in Patients With Sickle Cell Disease

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of three dose levels of HQK-1001 administered once daily for 26 weeks in subjects with sickle cell disease.

NCT ID: NCT01283139 Completed - Clinical trials for Systemic Lupus Erythematosus

A Study to Evaluate the Efficacy and Safety of Sifalimumab in Adults With Systemic Lupus Erythematosus

Start date: March 31, 2011
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of sifalimumab compared to placebo in subjects with moderately to severely active Systemic Lupus Erythematosus (SLE).

NCT ID: NCT01171495 Completed - Clinical trials for Human Immunodeficiency Virus (HIV)

Impact of Nutrition Intervention on HIV/AIDS Infected Patients

INI
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Intervention to investigate the efficacy of a nutritional supplement among ARV-naïve, asymptomatic HIV positive patients with a CD4 count in the range 300-550 cells/ul.

NCT ID: NCT01151891 Completed - Diabetes Clinical Trials

Natural History of Pedal Puncture Wounds in Diabetics

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

There are no evidence (research) based guidelines for treatment of early, closed puncture wounds of the feet in diabetics. Surgeons usually see only the limb- and life-threatening consequences of puncture wounds of the feet in diabetics, and are therefore tempted to advocate more aggressive, preemptive, invasive primary treatment for all such wounds, assuming, from this blinkered perspective that all such wounds progress to serious infection. This study is designed to determine the natural history of puncture wounds of the feet in diabetics, specifically, whether all become infected or whether some do heal without any surgical intervention. It requires administration of a questionnaire to 188 known diabetics attending 11 selected outpatient health care centers in the parish of St. James, Jamaica.

NCT ID: NCT00842088 Completed - Sickle Cell Disease Clinical Trials

Phase 1/2 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of HQK-1001 Administered Daily in Patients With Sickle Cell Disease

Start date: March 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and tolerability of HQK-1001 administered for a total of 12 weeks (with one dosing break) in subjects with sickle cell disease.

NCT ID: NCT00818935 Completed - Type 2 Diabetes Clinical Trials

Low-Intermediate-Glycemic Index Caribbean Foods Versus High Glycemic Index Foods in Type 2 Diabetes

Start date: June 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether low and intermediate GI Caribbean foods are effective in the management of type 2 diabetes.

NCT ID: NCT00429351 Completed - Kwashiorkor Clinical Trials

Aromatic Amino Acid Metabolism in the Pathogenesis of Kwashiorkor

Start date: September 2006
Phase:
Study type: Observational

This research may explain whether a shortage of three special compounds called aromatic amino acids is responsible for the severe illness and high death rate of children with the kwashiorkor type of malnutrition and whether supplying adequate amounts of these compounds in the treatment diet will speed up recovery from this condition. We propose that decreased availability of the aromatic amino acids may be the reason why children with kwashiorkor are sicker and more difficult to treat.

NCT ID: NCT00409890 Completed - Labor Stage, First Clinical Trials

The Effect of Hyoscine Butyl Bromide on the First Stage of Labor in Term Pregnancies

Start date: June 2005
Phase: Phase 2
Study type: Interventional

To determine whether hyoscine butyl bromide is effective in shortening the first stage of labor, with no increase in maternal or neonatal complications.