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Induction of labor by oral misoprostol solution

A Randomized control study of titrated and static oral misoprostol solution for induction of labor at term

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047385
Enrollment
Unknown
Registered
2021-06-13
Start date
2017-12-01
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Induction of labor

Interventions

titrated oral misoprostol solution versus static-dose oral misoprostol solution:titrated oral misoprostol solution versus static-dose oral misoprostol solution

Sponsors

Dr Barbie Sharma
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) Singleton live pregnancy; 2) >=37 weeks gestation; 3) Cephalic presentation; 4) Reactive NST 5) Modified Bishops score <=6.

Exclusion criteria

Exclusion criteria: 1) Hypersensitivity to misoprostol; 2) Uterine scar due to previous cesarean section or other uterine surgery; 3) Grand multipara; 4) Multiple gestations; 5) High risk pregnancies preeclampsia with severe features significant maternal cardiac, renal, liver disease; 6) Any contraindication to induction and vaginal delivery e.g. cephalopelvic disproportion, malpresentation, fetal compromise and ante partum hemorrhage; 7) Intrauterine fetal demise.

Design outcomes

Primary

MeasureTime frame
Induction to delivery time;—

Countries

India

Contacts

Public ContactDr Barbie Sharma

Christian Medical College and Hospital, Ludhiana, Punjab

barbiesharma.9@gmail.com+91 88 00328108

Outcome results

None listed

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