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1.
Ultrasound Obstet Gynecol ; 30(5): 697-705, 2007 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17899571

RESUMEN

OBJECTIVE: To investigate the efficacy of vaginal progesterone to prevent early preterm birth in women with sonographic evidence of a short cervical length in the midtrimester. METHODS: This was a planned, but modified, secondary analysis of our multinational, multicenter, randomized, placebo-controlled trial, in which women were randomized between 18 + 0 and 22 + 6 weeks of gestation to receive daily treatment with 90 mg of vaginal progesterone gel or placebo. Cervical length was measured with transvaginal ultrasound at enrollment and at 28 weeks of gestation. Treatment continued until either delivery, 37 weeks of gestation or development of preterm rupture of membranes. Maternal and neonatal outcomes were evaluated for the subset of all randomized women with cervical length < 28 mm at enrollment. The primary outcome was preterm birth at

Asunto(s)
Cuello del Útero/anomalías , Nacimiento Prematuro/prevención & control , Progesterona/administración & dosificación , Progestinas/administración & dosificación , Adulto , Método Doble Ciego , Femenino , Humanos , Embarazo , Resultado del Embarazo , Embarazo de Alto Riesgo , Cremas, Espumas y Geles Vaginales
2.
Ultrasound Obstet Gynecol ; 30(5): 687-96, 2007 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17899572

RESUMEN

OBJECTIVE: Preterm birth is the leading cause of perinatal morbidity and mortality worldwide. Treatment of preterm labor with tocolysis has not been successful in improving infant outcome. The administration of progesterone and related compounds has been proposed as a strategy to prevent preterm birth. The objective of this trial was to determine whether prophylactic administration of vaginal progesterone reduces the risk of preterm birth in women with a history of spontaneous preterm birth. METHODS: This randomized, double-blind, placebo- controlled, multinational trial enrolled and randomized 659 pregnant women with a history of spontaneous preterm birth. Between 18 + 0 and 22 + 6 weeks of gestation, patients were assigned randomly to once-daily treatment with either progesterone vaginal gel or placebo until either delivery, 37 weeks' gestation or development of preterm rupture of membranes. The primary outcome was preterm birth at

Asunto(s)
Aborto Habitual/prevención & control , Nacimiento Prematuro/prevención & control , Progesterona/administración & dosificación , Progestinas/administración & dosificación , Administración Intravaginal , Adolescente , Adulto , Algoritmos , Método Doble Ciego , Femenino , Humanos , Placebos , Embarazo , Resultado del Embarazo , Embarazo de Alto Riesgo , Cremas, Espumas y Geles Vaginales
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