None listed
Conditions
Interventions
Intervention1: nil: nil
Control Intervention1: nil: nil
Sponsors
ICST Corporation
Eligibility
Inclusion criteria
Inclusion criteria: Healthy non pregnant women
Exclusion criteria
Exclusion criteria: 1. Women diagnosed with breast cancer 2. Pregnant women 3. Women below 40 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The Primary end points are the sensitivity, specificity, accuracy and the positive and negative predictive values of the Breast cancer screening tools.Timepoint: 24 months | — |
Secondary
| Measure | Time frame |
|---|---|
| The Secondary end-point are a) Detection rates for detecting any breast lesion & suspicious breast lesions by the two screening methods. b) Concordance of conventional clinical Breast examination [CBE] with that using the Breast Care Glove by Trained PHW Timepoint: 24 months | — |
Countries
India
Contacts
Public ContactDr Vandita Pahwa
Homi Bhabha Cancer Hospital and Research Centre
Outcome results
None listed