None listed
Conditions
Interventions
Intervention1: NIL: Till date there have been a couple of studies to evaluate the monocular colposcope and compare its performance in detection of cervical neoplasias to that of conventional colposcop
Sponsors
Cervical Cancer Prevention and Control Initiative CPCI Project
Eligibility
Inclusion criteria
Inclusion criteria: 1. Women aged between 30 to 60 years 2. Intact Uterus 3. Non Pregnant
Exclusion criteria
Exclusion criteria: 1. Pregnancy 2. Past history of cervical pre cancer and /cancer treatment 3. Women refused to give informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To determine the sensitivity of gynocular in detecting cervical high grade lesions and cancers 2. To evaluate the agreement between diagnosis of different grades of cervical neoplasias made by gynocular and cervical histopathology Timepoint: 1 year | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the agreement between diagnosis of different grades of cervical neoplasias made by gynocular and cervical histopathology Timepoint: 2 YEARS | — |
Countries
India
Contacts
Public ContactDipanwita Banerjee
CHITTARANJAN NATIONAL CANCER INSTITUTE
Outcome results
None listed