Clinical Trials Directory

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UnknownNCT01156948

Misoprostol For Nulliparous Women Before Hysteroscopy

Comparison of Vaginal Versus Oral Misoprostol for Nulliparous Women Prior to Operative Hysteroscopy

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Wenzhou Medical University · Academic / Other
Sex
Female
Age
16 Years – 40 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGmisoprostol400ug vaginally the day before surgery
DRUGoral misoprostol400ug misoprostol orally the day before the surgery

Timeline

Start date
2008-05-01
Primary completion
2010-08-01
Completion
2011-12-01
First posted
2010-07-05
Last updated
2010-07-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01156948. Inclusion in this directory is not an endorsement.