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Immediate and delayed side effects in blood donors after blood donation.

Study of immediate and delayed adverse donors reactions in voluntary whole blood donors.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2016/09/007320
Enrollment
1000
Registered
2016-09-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

None listed

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Donors who meet the acceptability criteria as whole blood donor will be included in the study as per the standard operating procedures (SOP) for Criteria of blood donor suitability/ selection of the department.

Exclusion criteria

Exclusion criteria: Donors who do not meet the acceptability criteria as whole blood donor will be excluded from the study as per the donor selection SOP of the department.

Design outcomes

Primary

MeasureTime frame
To identify high risk group for anticipated donor reactions that can lead to better preventive strategies. It can also be used to evaluate and potentially improve blood donor safety and comfort.Timepoint: To identify high risk group for anticipated donor reactions that can lead to better preventive strategies. It can also be used to evaluate and potentially improve blood donor safety and comfort. In the long run, this will help us in enhancing donor satisfaction and donor retention and thus ensuring continuous blood supply.

Secondary

MeasureTime frame
In the long run, this will help us in enhancing donor satisfaction and donor retention and thus ensuring continuous blood supply.Timepoint: 2 to 3 months

Countries

India

Contacts

Public ContactDr Priti D Desai

Tata Memorial Hospital

anu.n198@gmail.com02224177000

Outcome results

None listed

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