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Comparison the effect of Letrozole with Misoprostol on induction of first trimester abortion in pregnancy

Comparison the effect of Letrozole plus Misoprostol with Misoprostol alone on induction of first trimester abortion in pregnant women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015050119037N8
Enrollment
70
Registered
2015-06-01
Start date
2014-11-22
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

Therapeutic Abortion. Therapeutic/Medical Abortion (termination of pregnancy)

Interventions

Intervention 1: First intervention group (control): Receiving 8 Misoprostol 100 mcg tablets as a single vaginal dose from Abureyhan drug manufacturing company, Iran. Intervention 2: Second interventio
Treatment - Drugs
First intervention group (control): Receiving 8 Misoprostol 100 mcg tablets as a single vaginal dose from Abureyhan drug manufacturing company, Iran
Second intervention group (trial): Receiving 4 Letrozole 2.5 mg tablets daily for 3 days (orally), from Abureyhan drug manufacturing company, Iran Plus Receiving 8 Misoprostol 100 mcg tablets as a

Sponsors

Investigator
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 34 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Pregnant women with 18 to 34 years of age with nonviable pregnancy under 12 weeks from the first day of last menstrual period. Exclusion criteria: History of systemic diseases or presence of acute conditions that require any urgent intervention and treatment.

Exclusion criteria

Exclusion criteria:

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 hour. Method of measurement: Physical examination.;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 ContactDr. Masoumeh Mohammadi

Kosar Obstetrics and Gynecology Hospital

mmohammadni@qums.ac.ir+98 28 3323 7267

Outcome results

None listed

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