Skip to content

To evaluate the safety of efficacy of different drugs in second trimester abortion

To evaluate the safety and efficacy of Mifepristone with Misoprostol versus Dinoprostone gel with Misoprostol in second trimester pregnancy termination in tertiary care centre

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/089975
Enrollment
60
Registered
2025-07-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: O04- Complications following (induced)termination of pregnancy

Interventions

Intervention1: Medical termination of pregnancy in second trimester by Mifepristone and Misoprostol: tab Mifepristone 200mg oral after 48hrs tab Misoprostol 400mcg per vagina every 3 hours to maximum

Sponsors

Dr Geetha Shree B
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant women between 18 to 45years seeking termination of pregnancy between 13-24 weeks of gestation fulfilling the prerequisites of Medical Termination of Pregnancy act 1971 and its amendments in 2021

Exclusion criteria

Exclusion criteria: Women with hemoglobin less than 8mg/dl Multiple Pregnancy Women with coagulation disorder Women with other medical disorders Incomplete abortion Patient with per vaginal leak Low lying placenta Patient with more than 1 previous cesarean section Intrauterine death Septic abortion Molar pregnancy Prior allergy to any of the drugs used in the study

Design outcomes

Primary

MeasureTime frame
To evaluate the safety and efficacy of Mifepristone and Misoprostol versus dinoprostone gel with Misoprostol in second trimester pregnancy termination; in terms of rate of complete abortion and induced abortion intervalTimepoint: One year

Secondary

MeasureTime frame
To compare & analyse need for surgical evacuation, uterine rupture, blood loss , sepsis, pain & need for analgesia between the study groupTimepoint: One year

Countries

India

Contacts

Public ContactDr Sunita Kittali

Belagavi institute of medical sciences

sunitamsog@gmail.com9480208858

Outcome results

None listed

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