Skip to content

Induction of abortion in the first trimester by misoprostol or misoprostol with different dose of letrozo

Induction of abortion in the first trimester by misoprostol or misoprostol with different dose of letrozol In women referring to Akbarabadi hospital in 1398-1399

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160523028008N13
Enrollment
114
Registered
2021-03-21
Start date
2021-05-05
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Medical abortion. Complication following abortion and ectopic and molar pregnancy,unspecified

Interventions

Intervention 1: Intervention group: Letrozole 10 mg and misoprostol tablets 800 mg three doses at intervals of three hours vaginal made by Abureyhan Pharmaceutical Company, Iran. Intervention 2: Inter

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age older than 18 years Gestational age based on ultrasound findings less than 12 weeks Patient and spouse satisfaction Lack of systemic diseases such as hypertension, kidney disease Hemoglobin greater than or equal to 10 g / l, diastolic blood pressure less than 95 mm Hg

Exclusion criteria

Exclusion criteria: Having an IUD Any allergy to letrozole or misoprostol Liver disease, kidney failure, high blood pressure and asthma Convulsions

Design outcomes

Primary

MeasureTime frame
The interval between induction and abortion beginning and opening of cervical internal os. Timepoint: Until 24 hours after receiving Misoprostol, every 1 hou. Method of measurement: Sonography.;The interval between induction and complete abortion. Timepoint: Until 24 hours after receiving Misoprostol, every 1 hour. Method of measurement: Sonography.

Secondary

MeasureTime frame
Gastrointestinal problems (nausea or vomiting). Timepoint: From receiving Letrozole until 24 hours after receiving Misoprostol. Method of measurement: Objective.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojgan Mokhtari

Iran University of Medical Sciences

mokhtari.m@iums.ac.ir+98 21 6655 2972

Outcome results

None listed

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