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NCT Number: NCT01801410

Induction With Foley OR Misoprostol (INFORM) Study

Between 40,000 and 80,000 pregnant women die annually from pre-eclampsia and eclampsia. Magnesium sulphate and anti-hypertensive therapies can reduce the morbidity associated with pre-eclampsia. The only cure, however, comes with delivery. Prompt delivery of the baby, preferably by vaginal route, is vital in order to achieve good maternal and neonatal outcomes. Induction of labour is therefore a critical intervention in order to prevent morbidity to both mother and baby. Two low cost interventions - oral misoprostol tablets and transcervical Foley catheterization - are already used by some in low resource settings, but their relative risks and benefits are not known. These interventions could optimize the care pathway for women needing induction of labour. This is especially important in low resource settings where improvement is most needed and the potential to reduce the maternal and neonatal mortality and morbidity is the greatest. The ideal induction agent would result in a relatively short induction to delivery interval without risk to fetus and with low rates of emergency caesarean section. The induction to delivery interval is especially important in pre-eclampsia and eclampsia where the condition may deteriorate rapidly until delivery. Inductions with prostaglandins, including misoprostol, are sometimes associated with uterine hyperstimulation and consequent fetal hypoxia, whilst the effectiveness and safety of Foley catheter as an induction agent has been persistently questioned. This study will identify the risk, benefits and trade-offs in efficacy, safety, acceptability and cost of these two low cost induction methods.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Daga Memorial Women's Hospital, Nagpur, Maharashtra, India

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About this study

This is a pragmatic, open-label, randomised control trial of two methods for labour induction among women with pre-eclampsia. Women requiring delivery for preeclampsia in two hospitals in Nagpur, India will be randomised to one of two treatment groups: transcervical Foley catheter or oral misoprostol tablets.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ongoing pregnancies with a live fetus in whom the decision has been made to induce vaginal delivery because of preeclampsia or uncontrolled hypertension. Women will be included irrespective of whether an intrapartum caesarean section on fetal grounds or would be considered or not.
  • Women age ≥18 years
  • Signed informed consent form

Exclusion criteria

  • • Women with previous caesarean sections
  • Those unable to give informed consent
  • Multiple pregnancy
  • History of allergy to misoprostol
  • Ruptured membranes
  • Chorioamnionitis (by clinical diagnosis)

Treatment and study plan

foley catheter

Device

Transcervical Foley catheter (silicone, size 18F with 30ml balloon)

Other names: Cervical ripening balloon, balloon catheter

Misoprostol

Drug

25mcg every 2 hours for maximum of 12 doses

Other names: Cytotec

Primary outcomes

  1. Attainment of vaginal delivery within 24 hours.

    Time frame: 24 hours

Sponsors and collaborators

Lead sponsor

University of Liverpool

Other

Collaborators

  • Daga Memorial Women's Hospital, Nagpur, India
  • Government Dental College and Hospital, India
  • Gynuity Health Projects

Registry information

Official study title

Induction of Labour in Pre-eclamptic Women: a Randomised Trial Comparing the Foley Balloon Catheter With Oral Misoprostol

Acronym: INFORM

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Feb 28, 2013
Registry last updated
Dec 14, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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