Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | misoprostol | 400ug vaginally the day before surgery |
| DRUG | oral misoprostol | 400ug 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.