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Effect of vaginal misoprostol in ease of doing hysteroscopy

Efficacy of vaginal Misoprostol in cervical priming in women undergoing vaginoscopic hysteroscopy : A Randomised Controlled Trialâ??

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/04/005666
Enrollment
108
Registered
2015-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Women undergoing diagnostic hysteroscopy fulfilling the selection criteria

Interventions

Intervention1: Group A:: Vaginal Misoprostol 200 microgram will be inserted 3 hours before the diagnostic hyseteroscopy Control Intervention1: Group B: No drug or medication will be administered int

Sponsors

JIPMER Government medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a. Age more than 18 years b. Women undergoing diagnostic hysteroscopy

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
1. Ease of cervical entryTimepoint: It will be recorded on a 5 point Likert scale

Secondary

MeasureTime frame
1. Pain perception using 10 point visual analog scale. 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. An assistant will check the procedure time.

Countries

India

Contacts

Public ContactDr Dilip Kumar Maurya

JIPMER

dilipkm2@gmail.com9442136037

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 7, 2026