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
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol | 1000 micrograms of self-administered vaginal misoprostol compared to placebo 12 hours before operative hysteroscopy after two weeks pretreatment with 25 micrograms daily vaginal oestradiol. |
| DRUG | Placebo | Vaginal 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.