Trials / Completed
CompletedNCT01612065
Optimum Misoprostol Dose Prior to Office Hysteroscopy
The Optimum Dose of Vaginal Misoprostol Prior to Office Hysteroscopy: Double Blind Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 132 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
Misoprostol is an effective agent for cervical priming before office hysteroscopy, vaginal route is the best, optimum dose not yet known.
Detailed description
The investigators will compare between 2 different doses of vaginal misoprostol, group (1) 200 ug, group (2) 400 ug, 3hours prior to office hysteroscopy , Infertile patient, patients with abnormal bleeding and patient with recurrent abortion Outcome measure: pain score, easiness of the procedure, procedure time, complications
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Misoprostol | 200 ug |
| DRUG | Misoprostol | Misoprostol vaginally, 400 ug |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2013-03-01
- Completion
- 2013-04-01
- First posted
- 2012-06-05
- Last updated
- 2013-04-11
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT01612065. Inclusion in this directory is not an endorsement.