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Pregnancy Complications clinical trials

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NCT ID: NCT00197730 Completed - HIV Infections Clinical Trials

Trial of Vitamins Among Children of HIV-infected Women

Start date: June 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the effects of multivitamin (B, C, E) supplementation on reducing the risk of morbidity and mortality outcomes among children born to HIV positive mothers, compared to placebo supplementation.

NCT ID: NCT00197561 Completed - HIV Infections Clinical Trials

Partnership on Nutrition and HIV/AIDS Research in Tanzania: Exploratory Research Study on Selenium and HIV Infection

Start date: September 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the oral administration of daily selenium supplements to HIV-1 positive pregnant women: enhances immune status and reduces the HIV-1 viral load at six months postpartum, reduces the risk of lower genital shedding of HIV-1 infected cells at 36 weeks of gestation, and reduces the risk of mastitis at six weeks postpartum, compared to placebo.

NCT ID: NCT00194311 Completed - Clinical trials for Pregnancy Complications

Human Papillomavirus (HPV) Infection in Pregnancy

Start date: April 2005
Phase: N/A
Study type: Observational

The purpose of this study is to determine if maternal infection with human papillomavirus (HPV) is associated with pregnancy complications including spontaneous preterm delivery (sPTD), severe preeclampsia (PE), and poor fetal growth.

NCT ID: NCT00194155 Completed - Clinical trials for Pregnancy Complications

Cytomegalovirus (CMV) Infection in Pregnancy

Start date: May 2003
Phase: N/A
Study type: Observational

The purpose of this study is to determine if (recurrent) cytomegalovirus (CMV) infection of the mother results in pregnancy complications such as preterm delivery, severe preeclampsia, poor fetal growth, or stillbirth.

NCT ID: NCT00194142 Completed - Clinical trials for Pregnancy Complications

Cytomegalovirus (CMV) Infection in Amniotic Fluid

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

The purpose of this study is to determine if detection of cytomegalovirus (CMV) in amniotic fluid collected in the second trimester of pregnancy is associated with pregnancy complications such as preterm delivery or severe preeclampsia.

NCT ID: NCT00190294 Completed - Clinical trials for Pregnancy Complications

Expectant Versus Immediate Medical Management for the Evacuation of the no Evolutionary Pregnancies Before 13 GW

Start date: April 2003
Phase: Phase 4
Study type: Interventional

Compared the interest of one week expectancy vs immediate medical treatment in the taking care of the evacuation of the no evolutionary pregnancies before 13 GW.

NCT ID: NCT00186082 Completed - Clinical trials for Pregnancy Complications, Infectious

Antibiotics for Postpartum Third and Fourth Degree Perineal Tear Repairs

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

This study is undertaken to find out whether prophylactic antibiotics can decrease the infection rate in third and fourth degree perineal tear repairs done in the immediate postpartum period.

NCT ID: NCT00114712 Terminated - Hepatitis C Clinical Trials

The Ribavirin Pregnancy Registry

RPR
Start date: January 2004
Phase:
Study type: Observational [Patient Registry]

Ribavirin should be avoided during pregnancy and during the 6 months before pregnancy in both the female and the male sexual partner. If a pregnancy occurs and is reported to the Ribavirin Pregnancy Registry, the Registry will follow the pregnant woman throughout pregnancy. The Registry will also follow the infant until 1 year of age. The goal of the Registry is to learn more about the effects of ribavirin on pregnancy and the risk for birth defects. Pregnant women exposed to ribavirin, either by taking ribavirin (during pregnancy or 6 months before pregnancy) or through a male sexual partner (who took ribavirin during the female partner's pregnancy or during the 6 months before pregnancy), are encouraged to contact the Registry.

NCT ID: NCT00028145 Completed - HIV Infections Clinical Trials

Prenatal and Postnatal Studies of Interventions for Prevention of Mother-To-Child Transmission

Start date: October 2002
Phase: N/A
Study type: Observational

The purpose of this study is to collect and study clinical and laboratory information about a pregnant or new mother and her medical care that will increase our knowledge of the best care for HIV-infected pregnant women and their children. The rate of transmission of HIV from mothers to their infants has gone down. Specific U.S. Public Health Service guidelines recommend that HIV-infected pregnant women be treated with anti-HIV therapies; but the effectiveness of treatment and safety for the mother and her infant have not been fully examined. This study will monitor the health of women and their infants while they receive anti-HIV therapy. Also, this study will provide information that may be used for future studies.

NCT ID: NCT00015002 Terminated - Clinical trials for Complications, Pregnancy

Repeat Antenatal Steroids Trial

BEARS
Start date: March 2000
Phase: Phase 3
Study type: Interventional

A course of steroids given to a mother who is in labor with a premature fetus will reduce the risk of the premature infant dying or having serious complications. This trial will test whether more than one course of antenatal steroids is more beneficial or risky to the infant than a single course.