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Comparison of two methods of hysteroscopy in women undergoing diagnostic hysteroscopy

Comparison of Standard Technique and Vaginoscopic Technique of Hysteroscopy in terms of intraoperative outcome in women undergoing Diagnostic Hysteroscopy under Anasthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099648
Enrollment
60
Registered
2025-12-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified

Interventions

Intervention1: Vaginoscopic Technique: Hysteroscopy performed using the vaginoscopiic (no touch) technique without the use of speculum or cervical instrumentation under anasthesia hysteroscope inserte

Sponsors

Lady Hardinge Medical College and SSKH Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women undergoing diagnostic hysteroscopy under general / regional anesthesia for indications such as abnormal uterine bleeding, infertility recurrent pregnancy loss or suspected intrauterine pathology (e.g. polyps, submucosal fibroids).

Exclusion criteria

Exclusion criteria: Women with previous history of surgeries involving cervix (e.g. H/o Manchester operation cervical conisation etc.) Pregnant women or those with suspected pregnancy. Presence of active pelvic infection or genital tract infection.

Design outcomes

Primary

MeasureTime frame
Time taken for hysteroscope entry into the uterine cavity (in minutes and second)Timepoint: Time taken for hysteroscope entry into the uterine cavity (in minutes and second)—

Secondary

MeasureTime frame
Proportion of women requiring Conversion of technique from group 2 to group 1. Proportion of women having intraoperative complications (cervical laceration, uterine perforation, bleeding) in both groups. Postoperative pain after 6 hours of procedure (using VAS).Timepoint: Intraoperative 6 hours post procedure—

Countries

India

Contacts

Public ContactDr Aishwarya Kpaur

Lady Hardinge Medical College SSKH

aish9kapur@gmail.com8851605061

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026