Effect of vaginal misoprostol in ease of doing hysteroscopy
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Women undergoing diagnostic hysteroscopy fulfilling the selection criteria
- Registration Number
- CTRI/2015/04/005666
- Lead Sponsor
- JIPMER Government medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 122
Inclusion Criteria
a. Age more than 18 years
b. Women undergoing diagnostic hysteroscopy
Exclusion Criteria
1.Recent or current pelvic inflammatory disease
2.Pregnancy
3.Active uterine bleeding
4.Recent uterine perforation
5.Known sensitivity to prostaglandins
6. Bronchial asthma, renal failure, or glaucoma
7.Previous cesarean delivery
8.Previous cervical surgery
9.Neurological disorders affecting the evaluation of pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Ease of cervical entryTimepoint: It will be recorded on a 5 point Likert scale
- Secondary Outcome Measures
Name Time Method 1. Pain perception using 10 point visual analog scale. <br/ ><br>2. Procedural time defined as the time from introduction of hysteroscope from external cervical os to visualization of uterine cavityTimepoint: Pain perception will be assessed using the visual analogue scale immediately after procedure. <br/ ><br>An assistant will check the procedure time.