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Premature Birth clinical trials

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NCT ID: NCT02477423 Completed - Clinical trials for Premature Birth of Newborn

A Randomized Controlled Trial Investigating if Antibiotic Use in the First 48 Hours of Life Adversely Impacts the Preterm Infant Microbiome

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether antibiotics given immediately after birth alter the development of the developing preterm infant's microbiome, which may further alter overall clinical outcomes.

NCT ID: NCT02476656 Completed - Preterm Birth Clinical Trials

Placental Inflammation in Prenatal Care

PINC
Start date: June 2015
Phase:
Study type: Observational

Objective of study is to explore expression of stress-related genes and inflammation in placentas and umbilical cord blood for women participating in group prenatal care compared with women receiving individual prenatal care.

NCT ID: NCT02473055 Completed - Clinical trials for Premature Birth of Newborn

Kangaroo Care and Premature Infant Sleep

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

90 preterm infants were randomly assigned to kangaroo care (skin-to-=skin, chest-to-chest) group (n=50) or control (remained in incubator, prone (n=40) for a pretest period of 2- 3 hours, then fed, then KC group was placed in KC and control group remained in incubator for a 2-3 hr test period. EEG measures of sleep, HR, and RR were taken. .

NCT ID: NCT02471482 Completed - Clinical trials for Premature Brain Oxygenation

Effect of Mozart Music on Cerebral Oxygenation and Behavioural Response of Premature Infants

Start date: December 2013
Phase: N/A
Study type: Interventional

This study is intended to see the effect of Mozart music on oxygen content of brain of premature infants once they achieve corrected gestation of 28-32 weeks and are clinically stable. Each baby is its own control. Difference of Oxygenation of brain will be measured during period with and without music. In addition behavioural response of baby will be recorded during intervention

NCT ID: NCT02470676 Not yet recruiting - Preterm Birth Clinical Trials

Cervical Pessary vs Vaginal Progesterone in Preventing Preterm Birth Among Women Presenting With Short Cervix: An Open-label Randomized Controlled Trial

Start date: July 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this randomized control trial is to determine whether cervical pessary plus vaginal progesterone is superior to vaginal progesterone alone in decreasing preterm delivery rate, and improving perinatal outcome, among women presenting with an asymptomatic mid-pregnancy short cervix, in singleton and twin gestations. All women with singleton or twin pregnancies undergoing routine ultrasonography up to 24 completed weeks of gestation (for examination of fetal anatomy and growth) and diagnosed with cervical length of ≤25 mm in singleton, or ≤38 mm in twins, will be invited to participate in the clinical trial. Women who meet eligible criteria will be invited to participate in the clinical trial. Women will be randomly assigned into one of the following groups: group A (vaginal progesterone) or group B (vaginal progesterone + pessary). Follow-up visits for ultrasound assessment of fetal growth and cervical length will be carried out every two weeks until 37 weeks of gestation.

NCT ID: NCT02469519 Completed - Premature Birth Clinical Trials

Impact of a Booster Course of Antenatal Steroids on Neonatal Outcome in Patients With Premature Rupture of the Membranes

ACSinPROM
Start date: March 3, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

This trial hopes to prospectively evaluate the impact of one versus two courses of antenatal steroids on the incidence of major neonatal morbidity in pregnant women with pre-labor premature rupture of the membranes.

NCT ID: NCT02452580 Active, not recruiting - Clinical trials for Premature Birth of Newborn

The Norwegian Family Centered Care Study

Start date: September 1, 2013
Phase:
Study type: Observational

This study evaluates possible effects of two different NICU designs; by comparing traditional and Family Centered Care in terms of infant nutrition, health and growth, and coping by family.

NCT ID: NCT02451228 Completed - Pregnancy Clinical Trials

Indomethacin PK and PD Therapy in Pregnancy

Start date: May 2015
Phase:
Study type: Observational

This study will follow pregnant women who are taking indomethacin as Standard of Care (SOC) for the indications of preterm labor (PTL), short cervix, or other indications, to evaluate the pharmacokinetics (PK), what the body does to the drug, and pharmacodynamics (PD), effectiveness of the drug in treating the specific intended disease process of this medication. This will help us develop more information for medication dosing specific to pregnant women experiencing preterm labor. Indomethacin is often prescribed to pregnant women presenting with preterm labor or shortened cervix, which places them at risk for preterm labor and delivery. Indomethacin has been used since the 1970s to prolong pregnancy by decreasing uterine contractions. However, despite the widespread use of indomethacin in pregnancy, there is limited information available to help physicians determine how much indomethacin to prescribe and how often to prescribe it.

NCT ID: NCT02441335 Completed - Preterm Birth Clinical Trials

CellulaR Injury and Preterm Birth

CRIB
Start date: January 2015
Phase:
Study type: Observational

The goal of this study is to examine how cellular dysfunction can lead to preterm birth. Women with singleton pregnancies with spontaneous preterm labor, preterm premature rupture of membranes, and cervical insufficiency (20 to 36-6/7 weeks gestation), and term deliveries (greater than 38 weeks) will be enrolled. Medical/obstetric history and pregnancy outcomes will be recorded. Maternal blood, urine and cervical cells (enrollment); cord blood and placental biopsy (delivery) will be collected.

NCT ID: NCT02438371 Terminated - Preterm Labor Clinical Trials

Nifedipine or Nifedipine Plus Indomethacin for Treatment of Acute Preterm Labor

Start date: May 2015
Phase: Phase 4
Study type: Interventional

Tocolytic agents are used for the treatment of preterm labor. It is unclear whether combination treatments of two tocolytic agents are more effective in stopping preterm labor compared to one. Therefore, the investigators propose a comparative effective trial of nifedipine plus indomethacin vs. nifedipine alone for the treatment of preterm labor