The Value of Pretreatment With Letrozole on Induction Time of Medical Evacuation With Misoprostol in Cases of Missed Abortion

ConditionLetrozole
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorCairo University

About this trial

The aim is to evaluate the effect of letrozole pretreatment on the induction time during medical evacuation using misoprostol in women diagnosed with missed abortion, and to compare its efficacy and safety to misoprostol alone.

Eligibility criteria

Qualifiers

Women aged 18 - 45 years.

Diagnosed with missed abortion confirmed by ultrasound (absent fetal heartbeat and/or no embryonic development).

Gestational age ≤ 12 weeks based on last menstrual period

Hemoglobin levels >10 g/dL.

Disqualifiers

Incomplete abortion, inevitable abortion, or threatened miscarriage.

Suspected ectopic pregnancy and molar pregnancy.

History of allergy or contraindication to misoprostol or letrozole.

Coagulopathy or use of anticoagulant medications.

Trial design

Treatments tested in this trial

  • Intervention Group: letrozole followed by misoprostol
  • Control Group: misoprostol only

Treatment groups

74 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators