Back to Search
Start Over
Trial protocol OPPTIMUM– Does progesterone prophylaxis for the prevention of preterm labour improve outcome?
- Source :
- BMC Pregnancy and Childbirth, Norman, J E, Shennan, A, Bennett, P, Thornton, S, Robson, S, Marlow, N, Norrie, J, Petrou, S, Sebire, N, Lavender, T & Whyte, S 2012, ' Trial protocol OPPTIMUM-Does progesterone prophylaxis for the prevention of preterm labour improve outcome? ', BMC pregnancy and childbirth, vol. 12, pp. 79 . https://doi.org/10.1186/1471-2393-12-79, BMC Pregnancy and Childbirth, Vol 12, Iss 1, p 79 (2012)
- Publication Year :
- 2012
- Publisher :
- Springer Science and Business Media LLC, 2012.
-
Abstract
- Background Preterm birth is a global problem, with a prevalence of 8 to 12% depending on location. Several large trials and systematic reviews have shown progestogens to be effective in preventing or delaying preterm birth in selected high risk women with a singleton pregnancy (including those with a short cervix or previous preterm birth). Although an improvement in short term neonatal outcomes has been shown in some trials these have not consistently been confirmed in meta-analyses. Additionally data on longer term outcomes is limited to a single trial where no difference in outcomes was demonstrated at four years of age of the child, despite those in the “progesterone” group having a lower incidence of preterm birth. Methods/Design The OPPTIMUM study is a double blind randomized placebo controlled trial to determine whether progesterone prophylaxis to prevent preterm birth has long term neonatal or infant benefit. Specifically it will study whether, in women with singleton pregnancy and at high risk of preterm labour, prophylactic vaginal natural progesterone, 200 mg daily from 22 – 34 weeks gestation, compared to placebo, improves obstetric outcome by lengthening pregnancy thus reducing the incidence of preterm delivery (before 34 weeks), improves neonatal outcome by reducing a composite of death and major morbidity, and leads to improved childhood cognitive and neurosensory outcomes at two years of age. Recruitment began in 2009 and is scheduled to close in Spring 2013. As of May 2012, over 800 women had been randomized in 60 sites. Discussion OPPTIMUM will provide further evidence on the effectiveness of vaginal progesterone for prevention of preterm birth and improvement of neonatal outcomes in selected groups of women with singleton pregnancy at high risk of preterm birth. Additionally it will determine whether any reduction in the incidence of preterm birth is accompanied by improved childhood outcome. Trial registration ISRCTN14568373
- Subjects :
- Research design
medicine.medical_specialty
Reproductive medicine
Placebo
lcsh:Gynecology and obstetrics
Study Protocol
03 medical and health sciences
Child Development
Obstetric Labor, Premature
0302 clinical medicine
Double-Blind Method
Pregnancy
Obstetrics and Gynaecology
Humans
Medicine
030212 general & internal medicine
Child
lcsh:RG1-991
Progesterone
030219 obstetrics & reproductive medicine
business.industry
Obstetrics
17-alpha-Hydroxyprogesterone
Incidence
Incidence (epidemiology)
Pregnancy Outcome
Obstetrics and Gynecology
medicine.disease
Child development
3. Good health
Administration, Intravaginal
Pregnancy Trimester, First
Short cervix
Systematic review
Research Design
Pregnancy Trimester, Second
Sample Size
Female
RG
Progestins
business
Subjects
Details
- ISSN :
- 14712393 and 14568373
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- BMC Pregnancy and Childbirth
- Accession number :
- edsair.doi.dedup.....06ac5826c8fc941103746f5b961c3a68
- Full Text :
- https://doi.org/10.1186/1471-2393-12-79