Status:
UNKNOWN
Misoprostol For Nulliparous Women Before Hysteroscopy
Lead Sponsor:
Wenzhou Medical University
Conditions:
Cervical Ripening
Eligibility:
FEMALE
16-40 years
Phase:
PHASE3
Brief 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 hysterosco...
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-admi...
Eligibility Criteria
Inclusion
- nulliparous women who are referred to outpatient hysteroscopy and who have given informed consent will be eligible for study recruitment.
Exclusion
- women with a known allergy to misoprostol.
Key Trial Info
Start Date :
May 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2011
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT01156948
Start Date
May 1 2008
End Date
December 1 2011
Last Update
July 8 2010
Active Locations (1)
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1
the 1st Affiliated Hospital of Wenzhou Medical College
Wenzhou, Zhejiang, China, 325000