Clinical Trials Logo

Chorioamnionitis clinical trials

View clinical trials related to Chorioamnionitis.

Filter by:

NCT ID: NCT00879190 Completed - Chorioamnionitis Clinical Trials

Ampicillin / Sulbactam vs. Ampicillin / Gentamicin for Treatment of Chorioamnionitis

Start date: May 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Chorioamnionitis is an infection of the placenta and amniotic membranes (bag of waters) surrounding the baby inside of a pregnant woman prior to delivery. This infection is somewhat common and is routinely treated with antibiotics given to the mother both before and after the baby is born. Currently it is not known what is the best choice of antibiotics to treat this type of infection, but commonly used treatments include Unasyn (ampicillin/sulbactam) or ampicillin/gentamicin. We plan to compare these two different antibiotic regimens to see if one is better than the other at treating and preventing bad outcomes from chorioamnionitis in women and babies.

NCT ID: NCT00814905 Completed - Chorioamnionitis Clinical Trials

Treatment of Chorioamnionitis After Delivery

Start date: November 18, 2008
Phase: N/A
Study type: Interventional

Chorioamnionitis occurs in 1% to 5% of term pregnancies and may complicate up to 25% of cases of preterm labor. The traditional regimen used to treat intra-amniotic infection is intravenous ampicillin 2g every 6 hours and intravenous gentamicin 1.5 mg/kg every 8 hrs until delivery . In the past the recommendation has been that the antibiotics be continued postpartum until 24-48 hours afebrile. More recent studies have looked at using a one time dose of antibiotics after delivery vs treating until 24-48 hours afebrile. There have been no studies comparing treatment of chorioamnionitis with antibiotics vs no treatment with antibiotics postpartum. The aim of this study is to compare no treatment vs treatment with one dose after a vaginal delivery and one dose of antibiotics vs a full course until 24 hours afebrile after a cesarean delivery complicated by chorioamnionitis. The hypothesis is that there will be no difference in outcome between the two groups in each arm. This is a randomized study. Once the patient delivers she will be randomized to one of two groups in each arm. First arm (vaginal delivery) A: no treatment, B: treatment with a one time dose of ampicillin/gentamicin; Second arm (c/s) A: one dose of ampicillin/gentamicin/clindamycin, B: treatment with ampicillin/gentamicin and clindamycin until 24 hours afebrile. The goal of the study is to determine the optimal postpartum management of chorioamnionitis.

NCT ID: NCT00724594 Completed - Brain Injury Clinical Trials

Safety of N-acetylcysteine in Maternal Chorioamnionitis (NAC in Chorio)

Start date: August 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this trial was to find the best dose of N-acetylcysteine (NAC) to decrease brain injury in babies exposed to intrauterine infection without causing significant side effects.

NCT ID: NCT00546195 Completed - Prematurity Clinical Trials

Infant Immune Response to Bacterial Infection

Start date: October 15, 2007
Phase: N/A
Study type: Observational

This study will examine the response of white blood cells to bacterial infection in blood taken from the umbilical cords of newly delivered infants. The blood samples will be taken from both male infants who were carried to term and male infants who were born prematurely, and genetic studies will compare these blood samples to samples drawn from healthy adult male volunteers. The study is designed to look at the ways in which the immune systems of newborn infants respond to bacterial infection. Participants in this study will be pregnant Chinese women admitted to the labor ward of the Prince of Wales Hospital (Sha Tin district of New Territories, Hong Kong SAR) for normal spontaneous delivery. Those with known blood-borne infectious diseases such as HIV and hepatitis B will be excluded from this study. Cord blood and placenta samples will be collected after the completion of delivery. The samples collected for this study will be restricted to male newborns. A comparison group of blood samples will be drawn from healthy male adults between 25 and 35 years of age....

NCT ID: NCT00397735 Completed - Inflammation Clinical Trials

N-acetylcysteine in Intra-amniotic Infection/Inflammation

Start date: October 1, 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the study is to determine if N-acetylcysteine (a potent free radical scavenger) prevents the occurrence of adverse neonatal outcomes in preterm deliveries complicated by infection associated with preterm labor or preterm premature rupture of membranes (PPROM). The working hypothesis is that in pregnancies complicated by intra-amniotic infection or inflammation, N-acetylcysteine protects the fetus by preventing the development, or decreasing the intensity and/or progression of the fetal inflammatory syndrome.

NCT ID: NCT00299637 Recruiting - Chorioamnionitis Clinical Trials

Changes in Blood Flow in MCA of Fetuses to Mothers Having Clinical Chorioamnionitis

Start date: October 2006
Phase: Phase 0
Study type: Observational

This study will try to determine whether fetuses to mothers having clinical chorioamnionitis have changes in blood flow in middle cerebral artery.

NCT ID: NCT00185991 Completed - Chorioamnionitis Clinical Trials

Comparison of Once Daily Versus 8 Hour Dosing of Gentamicin for the Treatment of Intrapartum Chorioamnionitis

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

To compare once daily versus 8 hour dosing of gentamicin for the treatment of chorioamnionitis.

NCT ID: NCT00153517 Completed - Premature Birth Clinical Trials

Maternal Effects of Bacterial Vaginosis (BV) Treatment in Pregnancy

Start date: October 1999
Phase: Phase 2
Study type: Interventional

The goal of this study is to examine acceptability and efficacy of 2 kinds of BV treatment among women at low risk for preterm delivery. The objectives are: 1. To examine the side effects and patient acceptability of oral versus intravaginal metronidazole. 2. To compare the efficacy of oral and intravaginal metronidazole for the treatment of BV 3. To study the efficacy of oral and intravaginal metronidazole for the prevention of hospital admission during the 3rd trimester, chorioamnionitis, preterm delivery, and maternal infectious morbidity.

NCT ID: NCT00070746 Completed - Pregnancy Clinical Trials

Perinatal Infections in Pakistan

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

There are large differences in health outcomes related to pregnancy and birth between developed and developing countries. This study will investigate how infections, medical history, health care behavior and psychosocial issues are associated with pregnancy outcomes in Pakistan.

NCT ID: NCT00021671 Completed - HIV Infections Clinical Trials

Antibiotics to Reduce Chorioamnionitis-Related Perinatal HIV Transmission

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see if antibiotic drugs given to treat an infection of the uterus during pregnancy can reduce the chances of HIV being passed from an HIV-positive mother to her baby. A link between bacterial disease of the vagina, premature birth, infection of the uterus during pregnancy, and the passing of HIV from a mother to her baby has been found. Early treatment of these problems may reduce the risk of passing HIV from an HIV-positive mother to her baby. [Note: As of 02/21/03, enrollment into this study was halted because preliminary data showed that the study antibiotics were not effective in preventing mother-to-child HIV transmission.]