Early universal use of oral progesterone for prevention of preterm births in singleton pregnancy (SINPRO study): protocol of a multicenter, randomized, double-blind, placebo-controlled trial

被引:6
|
作者
Cheung, Ka Wang [1 ]
Seto, Mimi Tin Yan [1 ]
Ng, Ernest Hung Yu [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, 6-F Prof Block,102 Pokfulam Rd, Hong Kong, Peoples R China
关键词
Preterm birth; Progesterone; Cervical length; Universal use; SONOGRAPHIC SHORT CERVIX; VAGINAL PROGESTERONE; SYSTEMATIC ANALYSIS; TIME TRENDS; WOMEN; RISK; EPIDEMIOLOGY; OUTCOMES; LENGTH;
D O I
10.1186/s13063-020-4067-z
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Preterm birth accounts for 75% of perinatal deaths and more than 50% of long-term neurological disabilities. For a singleton pregnancy, progesterone treatment is effective in prevention of preterm birth in women with an asymptomatic short cervix or a history of preterm birth. However, a large proportion of preterm births still is not currently preventable. The aim of this study is to determine whether early universal use of oral progesterone before 14 + 0 weeks of gestation can prevent preterm birth better than universal screening of cervical length at 18 + 0 to 23 + 6 weeks of gestation, followed by progesterone treatment in those with a short cervix in singleton pregnancy. Methods This is a multicenter, randomized, double-blind, placebo-controlled trial registered with ClinicalTrials.gov on 12 February 2018. Eligible consecutive pregnant women with singleton gestation attending antenatal outpatient clinics will be recruited after receiving counseling and signing the written consent form. Transvaginal cervical length measurement will be performed at recruitment (before 14 + 0 weeks of gestation) and between 18 + 0 and 23 + 6 weeks of gestation. After randomization, women will be randomly assigned to either the treatment group (oral dydrogesterone 10 mg three times daily) or the placebo group, and medication will be started before 14 + 0 weeks of gestation. Assigned groups will be unblinded if the cervical length is <= 25 mm between 18 + 0 and 23 + 6 weeks of gestation, and the management option for short cervix will be discussed (oral progesterone, vaginal progesterone, or cervical cerclage). The primary outcome is preterm birth before 37 + 0 weeks of gestation. Discussion Progesterone is used extensively in part of the in vitro fertilization program as luteal phase support, and it is not associated with teratogenicity. Universal progesterone supplementation may be a better approach to prevent preterm birth. This large, multicenter, randomized, double-blind, placebo-controlled trial will provide the best evidence, leading to the best strategy for the prevention of preterm birth.
引用
收藏
页数:7
相关论文
共 50 条
  • [41] Prevention of radiotherapy induced enteropathy by probiotics (PREP): protocol for a double-blind randomized placebo-controlled trial
    Yeon Joo Kim
    Jesang Yu
    Sung Pyo Park
    Seung Hae Lee
    Young Seok Kim
    BMC Cancer, 21
  • [42] Double-blind randomized placebo-controlled trial of sibutramine
    Bray, GA
    Ryan, DH
    Gordon, D
    Heidingsfelder, S
    Cerise, F
    Wilson, K
    OBESITY RESEARCH, 1996, 4 (03): : 263 - 270
  • [43] Randomized, double-blind, placebo-controlled trial of nicotine replacement therapy in pregnancy
    Kapur, B
    Hackman, R
    Selby, P
    Klein, J
    Koren, G
    CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, 2001, 62 (04): : 274 - 278
  • [44] PYRIDOXINE FOR NAUSEA AND VOMITING OF PREGNANCY - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL
    VUTYAVANICH, T
    SUPREEYA, W
    RUANGSRI, R
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1995, 173 (03) : 881 - 884
  • [45] Duloxetine in the Prevention of Depressive Recurrences: A Randomized, Double-Blind, Placebo-Controlled Trial
    Perahia, David G. S.
    Maina, Giuseppe
    Thase, Michael E.
    Spann, Melissa E.
    Wang, Fujun
    Walker, Daniel J.
    Detke, Michael J.
    JOURNAL OF CLINICAL PSYCHIATRY, 2009, 70 (05) : 706 - 716
  • [46] Topiramate for migraine prevention in children: A randomized, double-blind, placebo-controlled trial
    Winner, P
    Pearlman, EM
    Linder, SL
    Jordan, DM
    Fisher, AC
    Hulihan, J
    HEADACHE, 2005, 45 (10): : 1304 - 1312
  • [47] A double-blind, randomized, placebo-controlled trial of olanzapine in the prevention of psychotic relapse
    Beasley, CM
    Sutton, VK
    Hamilton, SH
    Walker, DJ
    Dossenbach, M
    Taylor, CC
    Alaka, KJ
    Bykowski, D
    Tollefson, GD
    JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2003, 23 (06) : 582 - 594
  • [48] Topiramate for the prevention of paediatric migraine: a randomized, double-blind, placebo-controlled trial
    Winner, P
    Pearlman, EM
    Linder, S
    Jordan, D
    Fisher, A
    Hulihan, J
    CEPHALALGIA, 2004, 24 (09) : 814 - 814
  • [49] Allopurinol in the prevention of ERCP pancreatitis: A randomized double-blind placebo-controlled trial
    Romagnuolo, J
    Bailey, RJ
    Mortimer, ST
    Todoruk, DT
    Ferguson, JP
    deGara, C
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2002, 97 (09): : S302 - S303
  • [50] 17-hydroxyprogesterone caproate for preterm rupture of the membranes: a multicenter, randomized, double-blind, placebo-controlled trial
    Combs, C. Andrew
    Garite, Thomas J.
    Maurel, Kimberly
    Abril, Diana
    Das, Anita
    Clewell, William
    Heyborne, Kent
    How, Helen
    Huang, Wilson
    Lewis, David
    Lu, George
    Miller, Hugh
    Nageotte, Michael
    Porreco, Richard
    Sheikh, Asad
    Tran, Lan
    AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2015, 213 (03)