Hysmis Study Misoprostol for cervical priming prior to hysteroscopy in postmenopausal or nulliparous women; a multi-centre randomised placebo controlled trial
Completed
- Conditions
- pain10029903hysteroscopy
- Registration Number
- NL-OMON39813
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 136
Inclusion Criteria
Indication for diagnostic or therapeutic hysteroscopy
Nulliparity if premenopausal
Postmenopausal state (>1 year after last menstruation)
Adequate command of the Dutch language
Informed consent
Exclusion Criteria
Allergy for Misoprostol
Previous cervical surgery
Active infection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Pain measured by a continuous pain score meter</p><br>
- Secondary Outcome Measures
Name Time Method