The preterm birth is considered as a main problem in the modern obstetrics, being the responsible of greatest of 50% neonatal morbimortality and heavy costs. Despite the significant medical advances, the rate of prematurity has not declined over the past 40 years and even continues to rise in the developed countries. In order to decrease the prematurity is necessary that two premises: to identify the pregnant women at risk of preterm birth, and dispose of useful measures aimed at prolonging the pregnancy and therefore avoid preterm delivery. The investigators propose a clinical trial with the objective to identify effective strategies to reduce the premature birth (34 weeks and earlier) rate in the population of pregnant women at risk for premature birth, which will be identified by ultrasound during the second trimester of their pregnancy. The investigators intend to compare two accepted strategies: administration of progesterone (vaginally) or the placement of vaginal pessaries. These 2 strategies are affordable, easy to apply, and they present very few maternal-fetal secondary effects.
The preterm birth is considered as a main problem in the modern obstetrics, being the responsible of greatest of 50% neonatal morbimortality and heavy costs. Despite the significant medical advances, the rate of prematurity has not declined over the past 40 years and even continues to rise in the developed countries. In order to decrease the prematurity is necessary that two premises: to identify the pregnant women at risk of preterm birth, and dispose of useful measures aimed at prolonging the pregnancy and therefore avoid preterm delivery. Since 1990, many published articles describe the sonographic measurement of the cervix from the week 16 as method of population screening to detect women at risk. Several studies provide evidence about an inverse relationship between the cervical length and the risk of preterm delivery. For this reason, if there is an effective intervention for patients with cervix short (about \< 25mm), made this measure in the middle of the second term, the investigators could reduce the prematurity. Regarding possible therapeutic strategies, recent published data demonstrate the effective of vaginal progesterone and cervical pessary in this population. However, both treatments have never been compared and none of the two strategies are indicated in this population. Therefore it results necessary to compare both treatments in order to establish clinical recommendations. The investigators propose a clinical trial to compare two accepted strategies: administration of progesterone (vaginally) or the placement of vaginal pessaries in order to reduce the premature birth (34 weeks and earlier) rate in the population of pregnant women at risk for premature birth, which will be identified by ultrasound during the second trimester of their pregnancy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
254
200 mg vaginal route per day
Cervical pessary certified by European Conformity (CE0482, MED/CERT ISO 9003/EN 46003;Dr Arabin, lower larger diameter 70 mm, height 30 mm,and upper smaller diameter 32 mm)
University Hospital San Juan de Alicante
Sant Joan d'Alacant, Alicante, Spain
University Hospital Quiron Dexeus
Barcelona, Barcelona, Spain
Igualada Hospital
Igualada, Barcelona, Spain
Burgos University Hospital
Burgos, Burgos, Spain
Ciudad Real General University Hospital
Ciudad Real, Ciudad Real, Spain
Guadalajara General University Hospital
Guadalajara, Guadalajara, Spain
University Hospital de León
León, León, Spain
University Hospital Príncipe de Asturias
Alcalá de Henarés, Madrid, Spain
University Hospital Fundación de Alcorcón
Alcorcón, Madrid, Spain
University Hospital Madrid Monte Principe
Boadilla del Monte, Madrid, Spain
...and 17 more locations
Proportion of spontaneous preterm birth before 34 weeks of gestation
Time frame: up to 11 weeks (from date of randomization until delivery)
Proportion of spontaneous preterm birth before 37 weeks of gestation
Time frame: up to 17 weeks (from date of randomization until delivery)
Proportion of Spontaneous preterm birth before 28 weeks of gestation
Time frame: up to 8 weeks (from date of randomization until delivery)
Rate of premature rupture of membranes before 34 weeks of gestation
Time frame: up to 11 weeks (from date of randomization until delivery)
Weight at birth
Time frame: up to 21 weeks (from date of randomization until delivery)
Rate of fetal and neonatal mortality
Time frame: From date of randomization until the date of delivery, assessed up 21 weeks
Symptomatic vaginal infections during treatment period
Time frame: From date of randomization until the date of delivery, assessed up 21 weeks
Proportion of participants with adverse events
Time frame: From date of randomization until the date of delivery, assessed up 21 weeks
Rate of Chorioamnionitis during third term
Time frame: From date of randomization until the date of delivery, assessed up 21 weeks
Need of admission because of premature labor before 34 weeks of gestation
Time frame: up to 14 weeks (from date of randomization until delivery)
Rate of neonatal morbidity
Time frame: From date of randomization until the date of delivery, assessed up 21 weeks
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