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Preterm Birth clinical trials

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NCT ID: NCT00163020 Completed - Preterm Birth Clinical Trials

17OHP for Reduction of Neonatal Morbidity Due to Preterm Birth (PTB) in Twin and Triplet Pregnancies

170HP
Start date: November 2004
Phase: Phase 2/Phase 3
Study type: Interventional

Hypothesis: Among women with twin or triplet pregnancies, weekly injections of 17-alpha-hydroxyprogesterone caproate (17OHP), started before 24 weeks of gestation, will reduce neonatal morbidity by reducing the rate of preterm delivery. This study involves two concurrent double-blinded randomized clinical trials of 17OHP versus placebo. Each trial will test the efficacy and safety of 17OHP in women with a specific risk factor for preterm birth. The two risk factors to be studied are: 1. Twin pregnancy 2. Triplet pregnancy

NCT ID: NCT00135902 Completed - Preterm Birth Clinical Trials

Omega-3 Fatty Acid Supplementation to Prevent Preterm Birth in High Risk Pregnancies

Start date: February 2005
Phase: Phase 3
Study type: Interventional

A recently completed trial of weekly injections of 17 alpha hydroxyprogesterone caproate (17P) found significant effectiveness for 17P in preventing recurrent preterm birth. However, the group who received 17P in this trial still had a high rate of preterm birth. Several reports have shown that dietary supplementation of fish oil, which is rich in Omega-3 fatty acids, reduces the risk of preterm birth. This trial tests whether adding the Omega-3 supplement to 17P therapy has the potential for further reducing the risk of preterm birth in women who have previously had a spontaneous preterm delivery. The trial will compare Omega-3 fatty acid with placebo in women receiving 17P therapy. The hypothesis being tested is: "Among women at high risk for preterm birth receiving weekly injections of 17P, the addition of Omega-3 nutritional supplement will further reduce the rate of preterm birth."

NCT ID: NCT00128141 Completed - Preterm Birth Clinical Trials

Effect of Tactile and Kinesthetic Stimulation on Very Low Birth Weight Preterm Infants

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

Two groups of preterm infants with birth weight equal to or less than 1500 grams will be studied. One group will receive the standard care and the other will receive standard care plus maternal special tactile stimulation. Gain of weight, length and head circumference, date of the beginning of enteral feedings, length of time to recover birth weight and age of hospital discharge will be recorded and compared between both groups.

NCT ID: NCT00120588 Completed - Preterm Birth Clinical Trials

Neuroprotection by Magnesium Sulfate Given to Women at Risk of Very Preterm Birth

Start date: July 1997
Phase: Phase 4
Study type: Interventional

Magnesium is neuroprotective in neonatal animal models of acquired hypoxic-ischemic and/or inflammatory cerebral lesions. It is associated with a significant reduction of perinatal death and cerebral palsy in some observational studies. The objective of the study is to assess if prenatal magnesium sulfate given to women at risk of preterm birth before 33 week's gestation is neuroprotective.

NCT ID: NCT00099164 Completed - Pregnancy Clinical Trials

Trial of Progesterone in Twins and Triplets to Prevent Preterm Birth (STTARS)

Start date: April 2004
Phase: Phase 3
Study type: Interventional

Women pregnant with twins or triplets are at high risk of preterm birth, yet no intervention or approach has served to reduce this risk. A recently completed trial by the NICHD sponsored Maternal Fetal Medicine Units (MFMU) Network has, for the first time, demonstrated a treatment that substantially reduces the rate of preterm birth in women at high risk for preterm delivery (i.e. progesterone therapy). Preterm birth was reduced by 35% among progesterone-treated women with a singleton pregnancy when compared with women receiving placebo. The current trial compares weekly treatment by injection of progesterone with placebo in women pregnant with twins or triplets.