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Induction With Foley OR Misoprostol (INFORM) Study

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

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01801410
Acronym
INFORM
Enrollment
602
Registered
2013-02-28
Start date
2013-12-31
Completion date
2015-06-30
Last updated
2015-12-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fetus or Newborn; Effects of Induction of Labor, Pre-eclampsia

Keywords

pre-eclampsia, labor induction, misoprostol, Foley catheter

Brief summary

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.

Detailed description

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.

Interventions

DEVICEFoley Catheter

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

DRUGMisoprostol

25mcg every 2 hours for maximum of 12 doses

Sponsors

Gynuity Health Projects
CollaboratorOTHER
Government Dental College and Hospital, India
CollaboratorOTHER_GOV
Daga Memorial Women's Hospital, Nagpur, India
CollaboratorOTHER
University of Liverpool
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frame
Attainment of vaginal delivery within 24 hours.24 hours

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026