None listed
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Society For Applied Studies
Eligibility
Inclusion criteria
Inclusion criteria: Pregnant women with any period of gestation, consenting for participation
Exclusion criteria
Exclusion criteria: Known cyanotic cardiac condition at the time of enrolment. Known jaundice at the time of enrolment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Agreement between hemoglobin estimation using a non-invasive point of care device and laboratory estimation of hemoglobin during pregnancyTimepoint: 24 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Agreement between ferritin estimation using a minimally-invasive point of care ferritin measurement device and laboratory estimation of serum ferritin during pregnancyTimepoint: 24 months;2. Stakeholder perceptions on acceptability of non-invasive hemoglobin measurement and anemia managementTimepoint: 24 months;3. Appropriate screening ranges for use of point-of-care non-invasive hemoglobin and minimally invasive ferritin assays as a screening tool for anemia during pregnancyTimepoint: 24 months;4. Estimation of potential cost saving from point-of-care non-invasive hemoglobin and minimally invasive ferritin assays as a screening tool for anemia during pregnancyTimepoint: 24 months | — |
Countries
India
Contacts
Public ContactDr Nidhi Goyal
Society for Applied Studies
Outcome results
None listed