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Preterm Delivery clinical trials

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NCT ID: NCT03596125 Terminated - Preterm Delivery Clinical Trials

Correction of Neonatal Glutathione by N-acetylcysteine in Pregnant Women at Risk of Premature Birth (GSH MAP)

Start date: November 5, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

Birth exposes the newborn to oxidative stress, as due to the switch from a protected, relatively hypoxic intrauterine milieu into an environment with a high oxygen pressure. The full-term newborn is well prepared to this massive redox challenge at the time of birth due to his well-integrated antioxidant defenses. On the contrary, numerous bibliographical data and our own work demonstrate the fragility of preterm newborns in this context of oxidative stress, linked to the immaturity of his antioxidant defenses. Premature birth abruptly propels the fetus from the protected, relatively hypoxic intrauterine milieu to an environment at risk of free radical injury caused by mechanical ventilation strategies, including the use of high inspired oxygen fractions or inhaled nitric oxide, generating excessive reactive oxidative species (ROS). Several studies highlight the key role of ROS in adverse outcomes of preterm infant suffering from low birth weight, bronchopulmonary dysplasia, necrotizing enterocolitis or retinopathy. This project aims to evaluate a therapeutic anti-oxidative strategy in order to correct the oxidative status of preterm infants. The investigators propose an early intervention that consists in an antenatal maternal supplementation with N-acetylcysteine (NAC), the acetylated precursor of both cysteine and glutathione, a key physiological antioxidant. This strategy could be promising for the development of simplified and personalized care of preterm infants. GSH MAP is a randomized, single-blind, placebo-controlled study that aims to determine if NAC supplementation in women admitted to hospital care due to preterm labor (prior to 34 weeks of gestational age) may correct glutathione deficiency in neonatal cord blood.

NCT ID: NCT02901626 Terminated - Preterm Delivery Clinical Trials

A Randomized Trial of Pessary in Singleton Pregnancies With a Short Cervix

TOPS
Start date: February 14, 2017
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine whether the Arabin pessary is a useful intervention of preterm birth at less than 37 weeks in women with a singleton gestation and a short cervix.

NCT ID: NCT02545127 Terminated - Preterm Delivery Clinical Trials

Merotocin in Mothers With Inadequate Milk Production and Infants Delivered Prematurely

MERMAID
Start date: May 28, 2021
Phase: Phase 2
Study type: Interventional

Induction and support of lactation in women with preterm delivery and inadequate milk production.

NCT ID: NCT00536003 Terminated - Morbidity Clinical Trials

Vaginal Progesterone to Prevent Preterm Delivery in Women With Preterm Labor

4P
Start date: July 2006
Phase: Phase 3
Study type: Interventional

The administration of vaginal progesterone, in addition to standard tocolysis, will decrease the risk of delivering prematurely and of recurrent preterm labor. We also hypothesize that the reduction in preterm delivery will be associated with a decrease in infant mortality and morbidity.

NCT ID: NCT00439374 Terminated - Preterm Delivery Clinical Trials

RCT of Progesterone to Prevent Preterm Birth in Nulliparous Women With a Short Cervix

SCAN
Start date: April 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see if giving progesterone medication to pregnant women, who have never delivered a baby after 19 weeks of pregnancy and who have a short cervix, lowers the risk of early delivery and improves the health of their baby.