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A Hospital based cross sectional study

Clinicopathological evaluation of post-menopausal bleeding: A hospital based prospective cross-sectional study at rural tertiary care center - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/084102
Enrollment
84
Registered
2025-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

None listed

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Suman Meena
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Postmenopausal women with c/o bleeding per vagina

Exclusion criteria

Exclusion criteria: Women with bleeding disorder/blood dyscrasia,Women on anticoagulant,Women with vaginal bleeding from vulval cause,Women with menopausal hormonal therapy Women with history of perineal trauma,Deranged liver function test, thrombocytopenia

Design outcomes

Primary

MeasureTime frame
To evaluate the clinical features in postmenopausal bleeding,To differentiate various histopathology finds in postmenopausal bleeding.Timepoint: 78 Weeks—

Secondary

MeasureTime frame
To observe the USG finding in postmenopausal bleeding, To co-relate the various histopathological finding with the clinical featuresTimepoint: 78 weeks—

Countries

India

Contacts

Public ContactNupur Mittal

Uttar Pradesh University of Medical Sciences

mittalnupur246@gmail.com8791282884

Outcome results

None listed

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