Same-day Cervical Preparation With Misoprostol Before Hysteroscopy

• Status: Unknown status
• Trial end date: 2017-07-01
• Target enrollment: 0
• Participant gender: Female

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.

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Wolfson Medical Center
• Treatments: Misoprostol

Criteria

Inclusion Criteria:

• Patients admitted for elective hysteroscopy (diagnostic/surgical) at Wolfson Medical Center

• Written consent supplied

Exclusion Criteria:

• Contraindications to prostaglandin treatment (severe asthma, glaucoma, severe cardiac disease, renal failure)

• Prostaglandin allergy

• Pregnancy

• Genital infection

• Space-occupying lesion in the endocervical canal

• Prior cervical surgery