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Obstetric Labor, Premature clinical trials

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NCT ID: NCT04532086 Not yet recruiting - Preterm Labor Clinical Trials

Uterocervical Angle and Preterm Labour

Start date: November 20, 2020
Phase:
Study type: Observational

To determine whether a novel ultrasonographic marker, uterocervical angle, correlates with risk of spontaneous preterm birth

NCT ID: NCT04404686 Not yet recruiting - Clinical trials for Obstetric Labor, Premature

Vaginal Indomethacin for Preterm Labor

TOCOMED
Start date: October 2020
Phase: Phase 2/Phase 3
Study type: Interventional

Indometacin is a cyclooxygenase agent from the NSAID family that has been used to treat preterm contractions since the 70's by preventing the synthesis of prostaglandins. It has been shown to be significantly more effective than placebo and postpone labor for 7-10 days, prolong pregnancies above 37 weeks of gestation and reduce numbers of small for gestational age neonates. Nifedipine is a calcium channel blocker agent that has been shown to reduce rates of labor within 48 hours from treatment. Previous studies comparing rectal Indometacin to oral nifedipine were inconclusive. Prostaglandins are synthesized in the uterus and the uterine cervix and therefore local administration of Indometacin may be more effective than other forms of administration, as been shown in a previous study. In this study we aim to compare vaginal Indometacin administration to a commonly used tocolytic agent, nifedipine.

NCT ID: NCT04105881 Not yet recruiting - Labor, Premature Clinical Trials

Correlation Between Vitamin D and B Regulatory Cell in Pregnancy

Start date: February 10, 2020
Phase:
Study type: Observational

During pregnancy , the maternal immune system is always confronted with fetal alloantigens. the immunological mechanisms that prevent the rejection of the fetus are still not under understood.

NCT ID: NCT04104984 Not yet recruiting - Preterm Labour Clinical Trials

Detection of Preterm Labour by Cervical Length

Start date: February 15, 2020
Phase: Early Phase 1
Study type: Interventional

Detection of short cervix by transvaginal ultrasound and its evidence based management to prevent preterm birth .

NCT ID: NCT03623685 Not yet recruiting - Preterm Labor Clinical Trials

UTEROCERVİCAL ANGLE MEASUREMENT IN SPONTANEOUS PRETERM BIRTH (UAMSPB)

UAMSPB
Start date: August 10, 2018
Phase: N/A
Study type: Interventional

İn this study Study; Between August 2018 and August 2019, the Ministry of Health, Medeniyet University, Göztepe Training and Research Hospital, Gynecology and Obstetrics Clinic Will be Included for Routine Control Purposes, Single Pregnancies Between 16-24 Weeks and no Known Risk Factors for Preterm Delivery . Each Participant Will be Given Written and Verbal Information About the Work and Will be Informed. Uterocervical Angle Measurement; Dorsolithotomy, Using a Sterilized Vaginal Ultrasonic Probe. It Will be Seen That the Distance Between the Internal Cervical os and the External Cervical os is Inclusive of the Cervical Isthmus That Can be Seen With the Anterior Uterine Wall. The First Line Will be Drawn Between the Internal Cervical os and the External Cervical os. The Second Line Will be Drawn as Passing Through the Internal Cervical Ostia, Parallel to the Anterior Uterine Wall. The Angle Between the Two Lines on the Internal Cervical Vertebra Will be Measured. Patients Will be Followed up Until the End of the 37th Gestational Week. The Gestation Week They Are Giving Birth Will be Recorded. Patients Were Then Classified as Before and After 37 Gestational Weeks and Uterocervical Angle Measurements Between 16-24 Gestational Weeks Were Compared.

NCT ID: NCT03047304 Not yet recruiting - Preterm Labor Clinical Trials

Magnesium Effect on Embryonal PR Interval

Start date: February 14, 2017
Phase: N/A
Study type: Interventional

Magnesium is a known treatment for neuroprotection in preterm labor before 32 week of gestation. High concentration of Magnesium in the blood stream known as cause of conduction abnormalities and ECG changes such us prolonged QT, QRS and PR in about. The goal of our work is to evaluate the PR intervals in embryos after maternal treatment with magnesium during preterm labor.

NCT ID: NCT02598323 Not yet recruiting - Premature Labour Clinical Trials

Prevention and Treatment of Premature Labour for Asymptomatic Pregnant Women

Echo-col
Start date: November 2015
Phase: N/A
Study type: Interventional

State of the question and research objective: International trials have shown that ultrasound measurement of the cervix identifies a population at high risk of preterm delivery. In case of short neck several types of treatments can be recommended: progesterone, the establishment of a strapping or pessary. These three treatments reduce the risk of preterm delivery. There is no French study. The objective of this study is to reduce prematurity in the PACA region Monaco-Corsica by introducing a routine ultrasound screening strategy asymptomatic short necks. Population concerned: All patients with active singleton pregnancy between 16 and 26 SA SA are eligible to ultrasound of the cervix. - Primary endpoint: delivery rate before 37 weeks. - Criteria secondary judgments rate of deliveries before 37 weeks, neonatal mortality morbidity. Expected result: a prematurity of 50%

NCT ID: NCT01985594 Not yet recruiting - Preterm Labor Clinical Trials

Utrogestan Versus Nifedipine as Tocolysis for Preterm Labor: a Randomised Controlled Trial

UTROGESTAN
Start date: November 2013
Phase: Phase 2
Study type: Interventional

RESEARCH HYPOTHESIS -Incidence of preterm delivery is lower in women treated with oral micronized progesterone (Utrogestan) as acute tocolysis agent compare to Nifedipine group with fewer maternal side effect

NCT ID: NCT01360034 Not yet recruiting - Clinical trials for Obstetric Labor, Premature

Nifedipine Versus Indomethacin in the Treatment of Preterm Labour

Start date: December 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study was to compare the effectiveness of nifedipine versus indomethacin as tocolytic for the treatment of preterm labour with short cervix (< 2.5cms).

NCT ID: NCT01022619 Not yet recruiting - Clinical trials for Gestational Diabetes

The Association Between High Risk Pregnancy and Sleep-disordered Breathing

Start date: January 2010
Phase: N/A
Study type: Observational

The aim of the present study is to establish, using polysomnographic criteria and prospective nature, whether sleep apnea in pregnancy is more prevalent in women with high risk pregnancies including preeclampsia, gestational diabetes, and pre-mature contractions, and to determine the effect of sleep disordered breathing in pregnancy on fetal outcome. The investigators' hypothesis is that sleep-disordered breathing is more prevalent in women with high risk pregnancy compared to those with uncomplicated pregnancy.