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Preterm Labor clinical trials

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NCT ID: NCT05612984 Withdrawn - Preterm Labor Clinical Trials

Calcium Aspirin Multiple Micronutrients (CAMMS) to Reduce Preterm Birth

CAMMS
Start date: April 1, 2024
Phase: Phase 3
Study type: Interventional

This trial will evaluate the impact of an integrated intervention of daily maternal calcium, aspirin, and multiple micronutrients (CAMMS) compared to iron-folic acid (IFA) during pregnancy on preterm birth and other adverse birth outcomes. Both interventions will be delivered through existing antenatal service platforms using context-specific strategies informed by formative research incorporating human-centered design processes to achieve high acceptability and high adherence, in three low-income countries with diverse contexts: Burkina Faso, Pakistan, and Zimbabwe.

NCT ID: NCT03122704 Withdrawn - Preterm Labor Clinical Trials

Group B Streptococcus (GBS) Infection and in Preterm Labor Women Conceived Through IVF

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

This is a cross - sectional study to determine the prevalence of GBS infection and associated factors in preterm labor women conceived through ART. 221 subjects will be involved.

NCT ID: NCT02351310 Withdrawn - Premature Birth Clinical Trials

Effectiveness of ACS in Extreme Preemies

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

This is a randomized prospective clinical study that will evaluate the effects of antenatal corticosteroid administration (ACS) vs. placebo in singleton pregnancies who are threatening to deliver prematurely between 22 0/7 and 23 6/7 weeks on admission with the goal of improving composite neonatal mortality and morbidity.

NCT ID: NCT01869361 Withdrawn - Preterm Labor Clinical Trials

Indomethacin for Tocolysis of Preterm Labor

Start date: August 1, 2020
Phase: Early Phase 1
Study type: Interventional

Indomethacin for tocolysis for 48 hours vs placebo

NCT ID: NCT01406197 Withdrawn - Preterm Labor Clinical Trials

Uterine Electrical Activity Before and After Progesterone Treatment for Preterm Labor

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

This study will examine the effects of various formulations of progesterone on uterine electromyographic (EMG) activity in pregnant patients in premature labor to determine if progesterone will suppress uterine electrical activity and which formulation may be best for inhibition of uterine activity. Patients will be monitored prior to treatment and following treatment (every 2 to 4 hours) with one of three different formulations of progesterone for up to two days. Patients will continue to be observed until they deliver. Comparisons will be for uterine EMG activity from before treatment to that following treatments at 2, 4, 8, 12 24 and 48 hours and times of delivery after treatments (hours or days following treatments). Comparisons between mean values for EMG activity between the various treatments at the various times will also be made.