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Obstetric Labor, Premature clinical trials

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NCT ID: NCT01829204 Recruiting - Bacterial Vaginosis Clinical Trials

Prospective Data Bank Creation to Study Vaginal Conditions

CRIPB-13-002
Start date: April 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to identify and elucidate the pattern and perhaps role of atypical proteins, cytokines and vaginal microbial flora in the pathogenic mechanisms involved in the development of vulvodynia, recurrent fungal and bacterial vaginosis and preterm labor.

NCT ID: NCT01773135 Completed - Clinical trials for Threatened Preterm Labor

Maternal Serum Level of ACTH as a Predictive Marker of Preterm Labor in Patients With Threatened Preterm Labor

PTL
Start date: January 2013
Phase: N/A
Study type: Observational [Patient Registry]

The aim of this study is use of ACTH as a predictive marker in patients of threatened preterm labor .

NCT ID: NCT01722760 Completed - Clinical trials for Bronchopulmonary Dysplasia

Tidal Neonatal NO, Vitamins A and D, and Infant Lung Disease - The AD-ON Study

Start date: August 2013
Phase: N/A
Study type: Observational

Children born prematurely are of greater risk of developing chronic lung disease (Bronchopulmonary Dysplasia). With an increase in the amount of premature children, we expect an increasing number of children with BPD. Today we do not have many ways of predicting or treating this condition, and the children are usually in hospital for several months after birth. Many are dismissed with home oxygen. Children with BPD are typically often re-submitted to hospital with respiratory disease the first couple of years, and some of them have problems throughout childhood and into adulthood. Other scientists have found a correlation between BPD and Chronic Obstructive Pulmonary Disease (COPD). The condition as well as the treatment (steroids), are associated with great risk of adverse effects as Cerebral Palsy, blindness, deafness and mental retardation. The investigators wish to find a safe way to identify the children in greater risk of developing BPD, who could therefore benefit from a more intensive treatment.An early diagnosis would increase the possibility of predicting the prognosis. Other studies have proven a connection between both low vitamin A and D and high exhaled nitrogen oxide (NO) with lung disease. With this trial the investigators wish to make a reference material for NO and vitamins A and D in infants admitted to the neonatal department at two hospitals in Denmark, both with and without treatment with nasal Continuous Positive Airway Pressure. The investigators furthermore wish to describe an eventual connection between BPD and these factors by examining a large group of children on 7 specific occasions within the first two months of life and at a one year follow up.

NCT ID: NCT01722708 Recruiting - Clinical trials for Abnormal Vaginal Flora

Comparison Between Oral Clindamycin Vs Metronidazole for the Treatment of Abnormal Vaginal Flora in High Risk Pregnancies

Start date: November 1, 2012
Phase: N/A
Study type: Interventional

Abnormal vaginal flora is a risk factor for preterm labor. Therefore, in high risk pregnancies for preterm labor the diagnosis and treatment of abnormal flora is indicated. Clindamycin and metronidazole given orally are both acceptable treatments in these cases. The purpose of this study is to compare the effectiveness of Clindamycin Vs metronidazole for the treatment of abnormal vaginal flora in high risk pregnancies. For this purpose, pregnant women who are considered high risk for preterm labor and were diagnosed with abnormal vaginal flora will be randomly treated either with clindamycin or metronidazole. Eradication of the abnormal flora and adverse effects will be monitored and compared

NCT ID: NCT01702376 Completed - Clinical trials for Obstetric Labour, Premature

This Study Will Investigate the Effect of Single Oral Doses of Retosiban on Cardiac Repolarization, With Moxifloxacin as a Positive Control in Healthy Volunteers.

Start date: October 3, 2012
Phase: Phase 1
Study type: Interventional

This will be a randomized, placebo-controlled, single, oral dose, four-way Williams crossover study design in healthy male and female subjects. The study consists of screening (28 days), treatment (1 day/dosing session) and follow-up (7 to 14 days) period and the total duration of study participation for each subject will be approximately 9 weeks. Each subject will participate in 4 dosing sessions separated by a minimum 7-day washout period. All subjects will receive single doses of retosiban 100 mg, (treatment A) retosiban 800 mg (Treatment B), moxifloxacin 400 mg (Treatment C) and placebo (Treatment D) in one of the four treatment sequences (ABDC, BCAD, CDBA, DACB) following a Williams design Twelve-lead ECGs and continuous Holter monitoring, clinical laboratory safety tests, vital sign measurements, physical examinations, adverse event reports, and pharmacokinetic samples will be collected throughout the study. In each study period, cardiac conduction will be measured using a 24-hour continuous 12-lead Holter monitor from the morning of Day 1 (dosing) until the morning of Day 2.

NCT ID: NCT01627587 Completed - Clinical trials for Obstetric Labour, Premature

A Two Cohort Study to Look at the Metabolites of GSK221149, the Metabolism of GSK221149 Administered With a High Fat Meal and With Ketoconazole

Start date: December 12, 2011
Phase: Phase 1
Study type: Interventional

This is a two part study. Part A of the study will evaluate the metabolites of GSK221149 following single and repeat oral dosing and will also assess the pharmacokinetics of GSK221149 when administered with a potent CYP3A4 inhibitor Ketoconazole. Part B of the study will look at the pharmacokinetics of GSK221149 following a high fat meal.

NCT ID: NCT01577121 Completed - Clinical trials for Preterm Labor With Intact Membranes

Evaluation of the Use of Indomethacin as Co-treatment in Women With Preterm Labor and High Risk of Intraamniotic Inflammation

INDOGEST
Start date: April 2012
Phase: Phase 2
Study type: Interventional

To demonstrate if indomethacin associated to conventional treatment for preterm labor is useful to delay delivery and to improve neonatal morbimortality in women with preterm labor with high risk of intraamniotic inflammation

NCT ID: NCT01523483 Completed - Preterm Birth Clinical Trials

Vaginal Progesterone for Prevention of Preterm Birth After an Episode of Preterm Labor

Start date: March 2012
Phase: N/A
Study type: Interventional

The investigators study objective is to investigate the effectiveness of vaginal micronized progesterone in prolonging pregnancy after an episode of preterm labor which responded to tocolytic treatment. Furthermore, the investigators aim is to study the mechanisms of actions of progesterone supplementation by examining its effect on the two components of parturition: cervical ripening and myometrial contractility. The investigators will utilize transvaginal ultrasound to assess the changes in the cervical tissue, and non-invasive trans-abdominal uterine EMG to assess the uterine muscle activity. The investigators will also look at the effect of progesterone on contraction frequency by tocodynamometer (TOCO), though EMG is expected to provide much more information.

NCT ID: NCT01518816 Recruiting - Preterm Labor Clinical Trials

Role of Serum Total Antioxidant Level in Preterm Labor

Start date: October 2011
Phase: N/A
Study type: Observational

The aim of this study is to detect the association between maternal serum antioxidant level and preterm labor.

NCT ID: NCT01431885 Completed - Preterm Labor Clinical Trials

Two Methods of Diagnosing Preterm Labor

Start date: August 2011
Phase: N/A
Study type: Interventional

Use of modern diagnostic tools e.g. fetal fibronectin and ultrasound measurement of cervical length to diagnose preterm labor can result in improved outcomes compared to traditional diagnosis based on digital examination to measure cervical change.