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Comparison of characteristics of women undergoing labor induction with oxytocin and oral misoprostol

Comparison of characteristics of women undergoing labor induction with oxytocin and oral misoprostol

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012080610511N1
Enrollment
65
Registered
2012-09-13
Start date
2010-02-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Induction of Labor. Failed medical induction of labour

Interventions

Intervention 1: First group received oral misoprostol, 25 mcg every 2 hours for up to 24 hours. Intervention 2: The oxytocin group recevied an infusion of 10 IU. Starting with four drops per minute,
Treatment - Drugs
First group received oral misoprostol, 25 mcg every 2 hours for up to 24 hours
The oxytocin group recevied an infusion of 10 IU. Starting with four drops per minute, which was doubled each quarter hour up to 64 drops.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 36 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 39 to 42 weeks of gestational age; Estimated fetal weight 4000 g; Normal fetal heart rate; cephalic presentation; Absence of uterine contractions; Singleton pregnancy; Bishop score of 7 or less. Exclusion criteria: Previous uterine surgery including caesarean section; Intrauterine fetal death IUGR; Oligohidroamnius; Placenta previa; Umbilical cord Prolapse; Corioamnionitis symptoms; Symptoms of active herpes; kidney or liver disease; NST Non-Stress Test reactive bread; Contraindication for Administration of prostaglandin. Contraindication for induction of labor; Vaginal bleeding of unknown cause.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Time of induction to active phase. Timepoint: During 12, 18, 24 hours. Method of measurement: clock.;Start time of induction to delivery. Timepoint: During 12, 18, 24 hours. Method of measurement: clock.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Maryam Karamali

Shahid Beheshti University of medical sceinces

dr.karamali@arakmu.ac.ir+98 21 2271 9013

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026