TY - JOUR
T1 - A Randomized Trial of Progesterone in Women with Bleeding in Early Pregnancy
AU - Coomarasamy, Arri
AU - Devall, Adam J
AU - Cheed, Versha
AU - Harb, Hoda
AU - Middleton, Lee J
AU - Gallos, Ioannis D
AU - Williams, Helen
AU - Eapen, Abey K
AU - Roberts, Tracy
AU - Ogwulu, Chriscasimir C
AU - Goranitis, Ilias
AU - Daniels, Jane P
AU - Ahmed, Amna
AU - Bender-Atik, Ruth
AU - Bhatia, Kalsang
AU - Bottomley, Cecilia
AU - Brewin, Jane
AU - Choudhary, Meenakshi
AU - Crosfill, Fiona
AU - Deb, Shilpa
AU - Duncan, W Colin
AU - Ewer, Andrew
AU - Hinshaw, Kim
AU - Holland, Tom
AU - Izzat, Feras
AU - Johns, Jemma
AU - Kriedt, Kathiuska
AU - Lumsden, Mary-Ann
AU - Manda, Padma
AU - Norman, Jane E
AU - Nunes, Natalie
AU - Overton, Caroline E
AU - Quenby, Siobhan
AU - Rao, Sandhya
AU - Ross, Jackie
AU - Shahid, Anupama
AU - Underwood, Martyn
AU - Vaithilingam, Nirmala
AU - Watkins, Linda
AU - Wykes, Catherine
AU - Horne, Andrew
AU - Jurkovic, Davor
N1 - Copyright © 2019 Massachusetts Medical Society.
PY - 2019/5/9
Y1 - 2019/5/9
N2 - BACKGROUND: Bleeding in early pregnancy is strongly associated with pregnancy loss. Progesterone is essential for the maintenance of pregnancy. Several small trials have suggested that progesterone therapy may improve pregnancy outcomes in women who have bleeding in early pregnancy.METHODS: We conducted a multicenter, randomized, double-blind, placebo-controlled trial to evaluate progesterone, as compared with placebo, in women with vaginal bleeding in early pregnancy. Women were randomly assigned to receive vaginal suppositories containing either 400 mg of progesterone or matching placebo twice daily, from the time at which they presented with bleeding through 16 weeks of gestation. The primary outcome was the birth of a live-born baby after at least 34 weeks of gestation. The primary analysis was performed in all participants for whom data on the primary outcome were available. A sensitivity analysis of the primary outcome that included all the participants was performed with the use of multiple imputation to account for missing data.RESULTS: A total of 4153 women, recruited at 48 hospitals in the United Kingdom, were randomly assigned to receive progesterone (2079 women) or placebo (2074 women). The percentage of women with available data for the primary outcome was 97% (4038 of 4153 women). The incidence of live births after at least 34 weeks of gestation was 75% (1513 of 2025 women) in the progesterone group and 72% (1459 of 2013 women) in the placebo group (relative rate, 1.03; 95% confidence interval [CI], 1.00 to 1.07; P = 0.08). The sensitivity analysis, in which missing primary outcome data were imputed, resulted in a similar finding (relative rate, 1.03; 95% CI, 1.00 to 1.07; P = 0.08). The incidence of adverse events did not differ significantly between the groups.CONCLUSIONS: Among women with bleeding in early pregnancy, progesterone therapy administered during the first trimester did not result in a significantly higher incidence of live births than placebo. (Funded by the United Kingdom National Institute for Health Research Health Technology Assessment program; PRISM Current Controlled Trials number, ISRCTN14163439.).
AB - BACKGROUND: Bleeding in early pregnancy is strongly associated with pregnancy loss. Progesterone is essential for the maintenance of pregnancy. Several small trials have suggested that progesterone therapy may improve pregnancy outcomes in women who have bleeding in early pregnancy.METHODS: We conducted a multicenter, randomized, double-blind, placebo-controlled trial to evaluate progesterone, as compared with placebo, in women with vaginal bleeding in early pregnancy. Women were randomly assigned to receive vaginal suppositories containing either 400 mg of progesterone or matching placebo twice daily, from the time at which they presented with bleeding through 16 weeks of gestation. The primary outcome was the birth of a live-born baby after at least 34 weeks of gestation. The primary analysis was performed in all participants for whom data on the primary outcome were available. A sensitivity analysis of the primary outcome that included all the participants was performed with the use of multiple imputation to account for missing data.RESULTS: A total of 4153 women, recruited at 48 hospitals in the United Kingdom, were randomly assigned to receive progesterone (2079 women) or placebo (2074 women). The percentage of women with available data for the primary outcome was 97% (4038 of 4153 women). The incidence of live births after at least 34 weeks of gestation was 75% (1513 of 2025 women) in the progesterone group and 72% (1459 of 2013 women) in the placebo group (relative rate, 1.03; 95% confidence interval [CI], 1.00 to 1.07; P = 0.08). The sensitivity analysis, in which missing primary outcome data were imputed, resulted in a similar finding (relative rate, 1.03; 95% CI, 1.00 to 1.07; P = 0.08). The incidence of adverse events did not differ significantly between the groups.CONCLUSIONS: Among women with bleeding in early pregnancy, progesterone therapy administered during the first trimester did not result in a significantly higher incidence of live births than placebo. (Funded by the United Kingdom National Institute for Health Research Health Technology Assessment program; PRISM Current Controlled Trials number, ISRCTN14163439.).
KW - Abortion, Spontaneous/prevention & control
KW - Administration, Intravaginal
KW - Adult
KW - Double-Blind Method
KW - Female
KW - Humans
KW - Live Birth
KW - Pregnancy
KW - Pregnancy Complications/diagnostic imaging
KW - Pregnancy Trimester, First
KW - Progesterone/administration & dosage
KW - Progestins/administration & dosage
KW - Treatment Failure
KW - Uterine Hemorrhage/drug therapy
U2 - 10.1056/NEJMoa1813730
DO - 10.1056/NEJMoa1813730
M3 - Article (Academic Journal)
C2 - 31067371
SN - 0028-4793
VL - 380
SP - 1815
EP - 1824
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 19
ER -