Misoprostol For Nulliparous Women Before Hysteroscopy

Status Recruiting

Clinical Trial Summary

To compare the impact of 400-microgram self-administered vaginal versus self-administered oral misoprostol at home on preoperative cervical ripening in nulliparous women prior to outpatient hysteroscopy.

Clinical Trial Description

There is no consensus on the effect of misoprostol on cervical ripening for nulliparous women. The aim of the study is to compare the impact of 400-microgram self-administered vaginal versus self-administered oral misoprostol at home on preoperative cervical ripening in nulliparous women prior to outpatient hysteroscopy. ;

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Cervical Ripening

Clinical Trial Details

NCT number	NCT01156948
Study type	Interventional
Source	Wenzhou Medical University
Contact
Status	Recruiting
Phase	Phase 3
Start date	May 2008
Completion date	December 2011

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See also
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