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Pregnancy clinical trials

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NCT ID: NCT00121394 Completed - Pregnancy Clinical Trials

Chlorhexidine Vaginal and Infant Wash in Pakistan

Start date: June 2005
Phase: Phase 3
Study type: Interventional

Infection is a major health problem during birth in Pakistan. This study will look at the possibility of using a septic wash to help improve health during birth in Karachi, Pakistan.

NCT ID: NCT00118027 Completed - Pregnancy Clinical Trials

A New Approach to Deliver Malaria Preventions to Pregnant Women at a Community Level in Uganda

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

SUMMARY Background: Malaria is the leading cause of morbidity and mortality among pregnant women in Uganda. Although effective tools for prevention and control of malaria exist, their delivery presents a problem. Intermittent presumptive treatment (IPT) with sulfadoxine-pyrimethamine (SP) is effective, yet >60% of women in Uganda do not get it as < 40%, attend antenatal care. Effective ways of delivering IPT with SP to pregnant women at a community level need to be developed. This study assessed whether community based resource persons like traditional birth attendants (TBAs), community reproductive health workers (CRHWs), adolescent peer mobilizers (APMs) and drug-shop owners (DSV) can distribute IPT with SP to pregnant women. Objectives: The objectives of this study were: - To assess community based approaches for delivering malaria prevention to pregnant women in Uganda; - To assess community perceptions, beliefs and practices associated with malaria treatment and prevention in pregnancy; - To assess whether community based resource persons can deliver IPT to pregnant women and reach those most at risk; - To assess the impact of IPT on anaemia and pregnancy outcome; - To estimate cost-effectiveness of the approaches and assess the acceptability and sustainability of the approaches. Methods: The study was conducted in 5 sub-counties of the Mukono district, situated on the shores of L. Victoria in Central Uganda. The district is hyper-endemic for malaria. 25 parishes with a total population of 75,000 people were used to test the new approaches. Phase 1 obtained qualitative data on community perceptions, beliefs and practices associated with malaria prevention in pregnancy. Phase 2 was an intervention study that assessed distribution of IPT to pregnant women by TBAs, CRHWs, APMs and DSVs compared with health units. Pregnant women of all parities were enrolled. Key resource persons in each parish were identified to sensitise the communities on the intervention. Data was collected regarding: timing of the first dose of SP, proportion of women who complete two doses of SP, birth weight of babies, proportion of low birth-weight babies, and proportion of adolescent pregnancies. The third phase of the study evaluated the sustainability of the approaches. Work Plan: The first phase of the study took two months. The second phase took 14-16 months. Data analysis was expected to take 12 months.

NCT ID: NCT00116272 Completed - Pregnancy Clinical Trials

Organization of Teratology Information Services (OTIS) Autoimmune Diseases in Pregnancy Project

Start date: April 2005
Phase:
Study type: Observational

The purpose of the study is to evaluate the effect of etanercept when used in the first trimester of pregnancy with respect to major structural birth defects of newborns. This is an observational study only - no investigational product is used.

NCT ID: NCT00115271 Completed - Pregnancy Clinical Trials

Antenatal Micronutrient Supplementation and Birth Weight

Start date: January 1999
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine the effects of providing supplements containing alternative combinations of micronutrients during pregnancy on birth weight and other infant and maternal health and nutritional outcomes in a rural area of Nepal.

NCT ID: NCT00114660 Completed - Pregnancy Clinical Trials

Cocoa Butter for Prevention of Stretch Marks

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

This study will check to see if using cocoa butter lotion on the belly, breasts and thighs will help reduce the appearance of stretch marks in pregnancy. Women entering the study will either receive a lotion containing cocoa butter with vitamin E or a lotion containing only vitamin E. After delivery, the study investigators will evaluate whether the women who used cocoa butter lotion were less likely to develop stretch marks.

NCT ID: NCT00099164 Completed - Pregnancy Clinical Trials

Trial of Progesterone in Twins and Triplets to Prevent Preterm Birth (STTARS)

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

Women pregnant with twins or triplets are at high risk of preterm birth, yet no intervention or approach has served to reduce this risk. A recently completed trial by the NICHD sponsored Maternal Fetal Medicine Units (MFMU) Network has, for the first time, demonstrated a treatment that substantially reduces the rate of preterm birth in women at high risk for preterm delivery (i.e. progesterone therapy). Preterm birth was reduced by 35% among progesterone-treated women with a singleton pregnancy when compared with women receiving placebo. The current trial compares weekly treatment by injection of progesterone with placebo in women pregnant with twins or triplets.

NCT ID: NCT00098709 Terminated - Pregnancy Clinical Trials

Fetal Pulse Oximetry Trial (FOX)

Start date: May 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the information provided to the physician by a fetal pulse oximeter during labor will reduce the chances of a cesarean delivery.

NCT ID: NCT00098202 Completed - Pregnancy Clinical Trials

Randomized Placebo-Controlled Trial (RPCT) of Maize/Zinc in Guatemala

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

Malnutrition is a serious health problem in the developing world. This study looks at the effects of changing the type of basic food staple (corn) used in Guatemala and infant zinc supplementation on infants' growth, development, and illnesses from infectious diseases.

NCT ID: NCT00097240 Completed - Pregnancy Clinical Trials

An Observational Study of the Use and Safety of Raptiva During Pregnancy (FOLLOW)

FOLLOW
Start date: January 2005
Phase: Phase 4
Study type: Observational

The Raptiva Pregnancy Registry was a prospective observational study established to obtain data on pregnancy outcomes of women who were exposed to Raptiva.

NCT ID: NCT00097123 Completed - Pregnancy Clinical Trials

RCT of Misoprostol for Postpartum Hemorrhage in India

Start date: September 2002
Phase: N/A
Study type: Interventional

Death rates for pregnant women in rural India are approximately forty-five times higher than in the United States. Bleeding after the birth of a child and underlying anemia are the primary causes of mothers' deaths and sickness in rural India. This study assesses the effectiveness of an oral drug, misoprostol, given in the late stage of labor to reduce the incidence of maternal bleeding following births assisted by midwives in selected sites in Belgaum District, Karnataka, India.