Clinical Trials Logo

Clinical Trial Summary

This is a randomized trial, assessing Misoprostol efficacy in cervical preparation several hours prior to hysteroscopy, comparing the different routes of administration (PO/PV/buccal). Initial cervical dilatation will be assessed, as well as surgical ease of dilatation, time required to achieve dilatation and patient preference.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Prevention


Related Conditions & MeSH terms

  • Cervical Preparation Prior to Hysteroscopy

NCT number NCT02474433
Study type Interventional
Source Wolfson Medical Center
Contact Hadas Ganer Herman, MD
Phone 972526206696
Email hadassganer@yahoo.com
Status Recruiting
Phase Phase 4
Start date July 2015
Completion date July 2017