Comparison of the effect of different timing of misoprostol tablet administration on softening of uterine cervix during hysteroscopic procedure
Not Applicable
- Conditions
- Health Condition 1: null- Women more than 18years of age undergoing Vaginoscopic Hysteroscopy in JIPMER
- Registration Number
- CTRI/2018/08/015430
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Women more than 18years
Undergoing vaginoscopic hysteroscopy in WCH JIPMER
Exclusion Criteria
Cervical stenosis
Previous LSCS
Contraindications to misoprostol
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Ease of entry into the cervix recorded on a 10-point visual analogue scale and 5-point Likert scale <br/ ><br>2. Pain perception, recorded by 10-point visual analogue scale and 11 point Numerical Rating Scale. <br/ ><br>3. Procedural time from introduction of scope through external cervical os to visualization of the uterine cavityTimepoint: Pain will be assessed at three time points (1) During the procedure (2) At the end of the procedure <br/ ><br>(3) 30 minutes after the completion of procedure. <br/ ><br>Ease of entry and procedural will be recorded at the of procedure.
- Secondary Outcome Measures
Name Time Method Procedural time <br/ ><br>Occurrence of side effectsTimepoint: Procedural time <br/ ><br>Occurrence of side effects