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comparison of two different routes of T.Misoprostol 25mcg in initation of labour pain.

comparison of oral versus sublingual misoprostol for cervical ripening and induction of labour

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/09/009632
Enrollment
80
Registered
2017-09-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- pregnant women

Interventions

None listed

Sponsors

kasturba medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant women with Singleton fetus; Cephalic presentation; Bishop Score < 6; Normal CTG

Exclusion criteria

Exclusion criteria: parity >3; Estimated fetal weight >3.5kg; Previous cesarean section; Non reassuring/abnormal fetal heart rate pattern

Design outcomes

Primary

MeasureTime frame
induction to delivery intervalTimepoint: 24 hours—

Secondary

MeasureTime frame
mode of the delivery, vaginal delivery within 24 hours, duration of labour, any side effects, birth weight, apgar score, neonatal intensive care unit admission.Timepoint: 24 hours—

Countries

India

Contacts

Public ContactDr Jyothi shetty

kasturba medical college

jthshetty@gmail.com9845973697

Outcome results

None listed

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