Vaginal progesterone reduces the rate of preterm birth in women with a sonographic short cervix: a multicenter, randomized, double‐blind, placebo‐controlled trial
National Institutes of Health · Wayne State University · +25 more institutions
Abstract
Women with a sonographic short cervix in the mid-trimester are at increased risk for preterm delivery. This study was undertaken to determine the efficacy and safety of using micronized vaginal progesterone gel to reduce the risk of preterm birth and associated neonatal complications in women with a sonographic short cervix.
This was a multicenter, randomized, double-blind, placebo-controlled trial that enrolled asymptomatic women with a singleton pregnancy and a sonographic short cervix (10-20 mm) at 19 + 0 to 23 + 6 weeks of gestation. Women were allocated randomly to receive vaginal progesterone gel or placebo daily starting from 20 to 23 + 6 weeks until 36 + 6 weeks, rupture of membranes or delivery, whichever occurred first. Randomization sequence was stratified by center and history of a previous preterm birth. The primary endpoint was preterm birth before 33 weeks of gestation. Analysis was by intention to treat.
Citation impact
- FWCI
- 50.68
- Percentile
- 100%
- References
- 115
Authors
26- SSSonia S. Hassan
National Institutes of Health, Wayne State University, Detroit Medical Center, Hutzel Women's Hospital, Eunice Kennedy Shriver National Institute of Child Health and Human Development
- RRRoberto RomeroCorresponding
National Institutes of Health, Wayne State University, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Michigan State University
- DVD. Vidyadhari
Mediciti Institute of Medical Sciences
- SFShalini Fusey
Government Medical College and Hospital
- JKJason K. Baxter
Thomas Jefferson University
Topics & keywords
- Medicine
- Placebo
- Obstetrics
- Cervix
- Gestation
- Randomization
- Gynecology
- Randomized controlled trial
- Good health and well-being