A comparative study of vaginal hyoscine butyl bromide and misoprostol on cervical ripening for gynecological intrauterine procedures
Phase 3
Recruiting
- Conditions
- Intrauterine interventions.Encounter for gynecological examinationZ01.4
- Registration Number
- IRCT20151228025732N68
- Lead Sponsor
- Semnan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
Age 18 to 55 years
Before menopause
Exclusion Criteria
Pregnancy
History of more than 3 deliveries
Anatomic abnormalities in the genital tract
Infection or wound visible in the cervix or vagina
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical diameter. Timepoint: Before and after the intervention. Method of measurement: The largest size of Hegar dilator that can be inserted without resistance and easily.;The amount of pain. Timepoint: Before and after the intervention. Method of measurement: Visual analogue scale for pain (0 to10).;Bleeding rate. Timepoint: Before and after the intervention. Method of measurement: Cylindrical (cc).
- Secondary Outcome Measures
Name Time Method