Misoprostol Prior to Office Hysteroscopy in Patients With no Risk Factors for Experiencing Unacceptable Pain

• Status: Unknown status
• Trial end date: 2015-10-01
• Target enrollment: 0
• Participant gender: Female

Summary

The aim of this study is to assess whether vaginal misoprostol reduces pain during office hysteroscopy in parous patients with no risk factors for experiencing severe or unacceptable pain.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Cairo University
• Treatments: Misoprostol

Criteria

Inclusion Criteria:

• Patients with at least one vaginal delivery who have an indication for office hysteroscopy.

Exclusion Criteria:

• Nulliparous patients, menopausal patients and patients with cervical pathology, and previous history of caesarean section or cervical surgery