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Premature Birth clinical trials

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NCT ID: NCT00579553 Completed - Premature Birth Clinical Trials

Comparing IM vs. Vaginal Progesterone for Pre-term Birth

Start date: October 2006
Phase: N/A
Study type: Interventional

This is a randomized controlled trial comparing weekly intramuscular injection of 17 alpha hydroxylprogesterone caproate with daily vaginal progesterone in women with singleton pregnancies and history of prior spontaneous preterm birth in terms of maternal, fetal and neonatal outcomes. Our aim is to assess the effects on maternal, fetal and neonatal outcomes of antenatal progesterone administered intramuscularly versus vaginally in women with singleton pregnancy and a history of prior preterm birth.

NCT ID: NCT00569530 Completed - Clinical trials for Bronchopulmonary Dysplasia

Trial of Late Surfactant to Prevent BPD: A Pilot Study in Ventilated Preterm Neonates Receiving Inhaled Nitric Oxide

TOLSURFPilot
Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the combination of late doses of Infasurf with inhaled nitric oxide will interact to improve the surfactant function and thus the respiratory status and outcome of treated infants.

NCT ID: NCT00568113 Completed - Preterm Labour Clinical Trials

N-Acetyl Cysteine for Prevention of Preterm Birth

NAC
Start date: July 2007
Phase: Phase 4
Study type: Interventional

The antioxidant effect of N-Acetyl cysteine can abort the inflammatory cascade responsible for initiation of preterm labour especially among patients with reccurent preterm birth and patients having bacterial vaginosis

NCT ID: NCT00556478 Completed - Clinical trials for Premature Ejaculation

Efficacy, Safety and Tolerability of PSD502 (a Topical Anesthetic) in the Treatment Premature Ejaculation

PSD502-PE-002
Start date: October 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness, safety and tolerability of the investigational drug, PSD502 in subjects with premature ejaculation (PE) The study drug, PSD02, is a metered dose (measured dose), topical (applied to the skin surface) anesthetic (numbing) spray containing a mixture of lidocaine and prilocaine. The study drug will be applied in a spray to the penis prior to intercourse in order to decrease sensitivity in an attempt to delay ejaculation.

NCT ID: NCT00549211 Completed - Clinical trials for Premature Ejaculation

A First Time in Human Study in Healthy Male Volunteers for Compound GSK557296.

Start date: October 2007
Phase: Phase 1
Study type: Interventional

A study conducted on healthy volunteers to determine the safety, tolerability and affect on the human body by experimental drug GSK557296.

NCT ID: NCT00537459 Completed - Clinical trials for Premature Ejaculation

A Study On Concentrations Of 16448 In Blood And The Safety Of This Compound In Healthy Males With Premature Ejaculation

Start date: December 2006
Phase: Phase 2
Study type: Interventional

16448 is being investigated for the treatment of primary premature ejaculation (PE) using a novel mode of action. There are no approved therapies for premature ejaculation, and novel therapies are needed for this syndrome. 16448 has been shown to increase ejaculatory latency in the PCA rat model of premature ejaculation. A novel instrument, the Sexual Assessment Monitor (SAM), will be used to measure ejaculatory latency time in this study. This device, which measures ELT under standard conditions, has been shown to provide a more reliable measure of ejaculatory latency compared to the use of a stopwatch during sexual intercourse

NCT ID: NCT00502697 Completed - Preterm Birth Clinical Trials

Tennessee Connections for Better Birth Outcomes

BBO
Start date: November 2006
Phase: N/A
Study type: Interventional

Women with a history of a prior preterm birth (PTB) have a high probability of a recurrent preterm birth. Some risk factors and health behaviors that contribute to PTB may be amenable to intervention. Home visitation is a promising method to deliver evidence based interventions. We evaluated a system of care designed to reduce preterm births and hospital length of stay in a sample of pregnant women with a history of a PTB. All participants (N = 211) received standard prenatal care. Intervention participants (N = 109) also received home visits by certified nurse-midwives guided by protocols for specific risk factors (e.g., depressive symptoms, abuse, smoking). Data was collected via multiple methods and sources including intervention fidelity assessments. Average age was 27.6 years. Racial breakdown mirrored local demographics. Most women had a partner, a high school education, and Medicaid. Enhanced prenatal care by nurse-midwife home visits may limit some risk factors and shorten intrapartum length of stay for women with a prior PTB. This study contributes to knowledge about evidence-based home visit interventions directed at risk factors associated with PTB.

NCT ID: NCT00497289 Completed - Preterm Infants Clinical Trials

Comparison of Two Different Lipid Emulsions for Parenteral Nutrition in Preterm Infants

Start date: January 2006
Phase: Phase 2
Study type: Interventional

The study shall provide evidence for the save and efficient use of a fish oil containing lipid emulsion in parenteral nutrition of preterm infants.Safety will be assessed by monitoring hepatological and hematological laboratory parameters. Efficiency will be assessed by monitoring of inflammatory parameters.

NCT ID: NCT00494702 Completed - Premature Birth Clinical Trials

Oxygen Toxicity in the Resuscitation in Extremely Premature Infants

OXTOX
Start date: April 2005
Phase: Phase 3
Study type: Interventional

The investigators hypothesize that using low oxygen concentrations during resuscitation of extremely premature infants will avoid oxidative stress derived damage and improve outcome.

NCT ID: NCT00494429 Completed - Premature Neonates Clinical Trials

Optimizing the Use of Morphine in Pre-Term Neonates

Start date: May 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to improve the dosing of morphine in critically ill premature neonates.