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Improving Cervical Cancer Screening in Women Living with HIV

Integration Of Cervical Cancer Screening With HPV Self Sampling Into Routine HIV Health Care Services Among Women Living With HIV In Maharashtra: An Implementation Research Mixed Methods Study - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/06/089264
Enrollment
600
Registered
2025-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: B20- Human immunodeficiency virus [HIV]disease

Interventions

Sponsors

Dr Sharmila Pimple
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Lab diagnosed HIV-positive women Female patients aged 25-65 years Non pregnant women

Exclusion criteria

Exclusion criteria: Past history of Cervical Cancer Pregnant Women

Design outcomes

Primary

MeasureTime frame
1. Sociodemographic Profile 2. Reproductive & Sexual history 3. High risk HPV prevalence HPVDNA 16, HPV DNA18, Other High-risk types 4. Conventional PAP cytology ASCUS, LSIL, HSIL, AGC, ASC-H, SCC 5. Prevalence of Acetowhite lesions through VIA with Mobile ODT 6. Acceptability of HPV self-sampling and Mobile ODT- - % of eligible women aware of cervical cancer screening. - % of eligible women screened through hrHPV self-testing. - % of eligible women screened through VIA with Mobile ODT. 7. Feasibility of HPV self-sampling and VIA with Mobile ODT: - Self-sample HPV DNA screening coverage - VIA with Mobile ODT screening coverage - Screen positive compliance with Reference diagnosis: Conventional CytologyTimepoint: 24 months

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Sharmila Pimple

Tata Memorial Hospital

pimplesharmila@gmail.com9223207939

Outcome results

None listed

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