None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Blood banks must be willing to participate and consent to the study. The blood banks must be located in geographically diverse regions. The blood banks must agree to use the BIMS system for the full duration of the study. Each blood bank must scan 200 blood bags using BIMS.
Exclusion criteria
Exclusion criteria: Blood banks that do not have the technical capability to implement BIMS. Blood banks that are not willing to participate for the entire study period. Blood banks with fewer than 200 blood bags to be scanned during the study period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of errors in blood grouping, viral screening, and avoidance of repeat donors by linking with phone or other identifiers.Timepoint: Month 1: Recruitment of blood banks, training sessions, and baseline data collection. Months 2-7: Implementation of BIMS, ongoing data collection, and monitoring. Month 8: Data analysis and review. Month 9: Report writing and dissemination of results. | — |
Secondary
| Measure | Time frame |
|---|---|
| Minimization of Blood Wastage Increased Transparency Improved Donor Communication System Integration Quality Assurance ImprovementTimepoint: Month 1: Recruitment of blood banks, training sessions, and baseline data collection. Months 2-7: Implementation of BIMS, ongoing data collection, and monitoring. Month 8: Data analysis and review. Month 9: Report writing and dissemination of results. | — |
Countries
India
Contacts
CR Healthcare