Clinical Trials Directory

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

TypeNameDescription
DRUGMisoprostol200 ug
DRUGMisoprostolMisoprostol 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.