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Clinical Trial Summary

Prospective interventional study where participants with non-viable pregnancy at 1st trimester will be randomized into two arms, one group will receive conventional treatment with oral mifepristone followed by misoprostol vaginally and another group will receive letrozole for three consecutive days followed by misoprostol vaginally in an attempt to terminate the pregnancy medically. Mean duration of induction to expulsion of product of conception and rate of complete abortion will be compared in two groups.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05304273
Study type Interventional
Source Calcutta National Medical College and Hospital
Contact Jhuma Biswas
Phone +91 9433019780
Email drjhumabiswas78@gmail.com
Status Recruiting
Phase Phase 3
Start date May 5, 2022
Completion date May 2024

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