FindTrial
Sign In

Comparing the diagnostic accuracy of hand-held colposcope with that of standard colposcope in detecting abnormal cervical lesions

Diagnostic accuracy of hand-held colposcope (Gynocular) in comparison with standard colposcope in women with abnormal cervical cytology or Visual Inspection with Acetic acid (VIA) positivity: a cross over randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022584
Enrollment
230
Registered
2019-12-31
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified

Interventions

Intervention1: Colposcopic examination under a hand-held colposcope: After obtaining informed consent, patients with abnormal cervical cytology or VIA or VILI positivity will be subjected to hand-held

Sponsors

Jawaharlal Institute of Postgraduare Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women between age 21-65 years attending Gynaecology Outpatient Department (OPD) with abnormal VIA or cervical cytology identified through pap smear

Exclusion criteria

Exclusion criteria: 1.Pregnant women 2.Women with ongoing vaginal bleeding 3.Patients with acute cervicitis 4.Patients with an obvious growth in cervix

Design outcomes

Primary

MeasureTime frame
Diagnostic accuracy of Gynocular colposcope comparison with standard colposcope in patients with abnormal cervical cytology or VIA positivity.Timepoint: 2-3 weeks—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactSowmiya J

Jawaharlal Institute of Postgraduate Medical Education and Research

muralidraiims@gmail.com8940760837

Outcome results

None listed

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