Health Condition 1: null- Women more than 18years of age undergoing Vaginoscopic Hysteroscopy in JIPMER
Conditions
Interventions
Intervention1: Group A (Short interval group): Misoprostol 200mcg vaginally, given 3hours prior to the hysteroscopy.
Control Intervention1: Group B, (Long interval group): Misoprostol 200mcg vaginally
Sponsors
JIPMER
Eligibility
Inclusion criteria
Inclusion criteria: Women more than 18years Undergoing vaginoscopic hysteroscopy in WCH JIPMER
Exclusion criteria
Exclusion criteria: Cervical stenosis Previous LSCS Contraindications to misoprostol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Ease of entry into the cervix recorded on a 10-point visual analogue scale and 5-point Likert scale 2. Pain perception, recorded by 10-point visual analogue scale and 11 point Numerical Rating Scale. 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 (3) 30 minutes after the completion of procedure. Ease of entry and procedural will be recorded at the of procedure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Procedural time Occurrence of side effectsTimepoint: Procedural time Occurrence of side effects | — |
Countries
India
Contacts
Public ContactDr Dilip Kumar Maurya
JIPMER
Outcome results
None listed