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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
74
Group A (Intervention Group) will receive letrozole followed by misoprostol.
Group B (Control Group) will receive misoprostol only, without prior letrozole pretreatment
Time of complete uterine evacuation
Time from misoprostol administration to complete uterine evacuation
Time frame: one week following Misoprostol administration
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