Clinical Trials Directory

Trials / Completed

CompletedNCT00572819

Hysteroscopy After Pretreatment With Misoprostol and Estradiol Trial

Does Self-Administered Vaginal Misoprostol Result in Cervical Ripening in Postmenopausal Women After 14 Days Pre-Treatment With Estradiol?

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Ullevaal University Hospital · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to investigate whether 1000 micrograms of self-administered vaginal misoprostol 12 hours before operative hysteroscopy results in effective preoperative cervical ripening after two weeks pretreatment with 25 micrograms daily vaginal estradiol, compared to placebo (lactosum monohydricum) in postmenopausal women.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostol1000 micrograms of self-administered vaginal misoprostol compared to placebo 12 hours before operative hysteroscopy after two weeks pretreatment with 25 micrograms daily vaginal oestradiol.
DRUGPlaceboVaginal lactosum monohydricum administered 24 hours in postmenopausal women, compared to misoprostol after two weeks pretreatment with 25 micrograms daily vaginal oestradiol.

Timeline

Start date
2008-01-01
Primary completion
2009-05-01
Completion
2009-05-01
First posted
2007-12-13
Last updated
2009-05-25

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT00572819. Inclusion in this directory is not an endorsement.