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Analysis of adverse events in voluntary platelet donors.

Analysis of immediate and delayed adverse events in voluntary platelet donors associated with plateletpheresis procedure.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/10/028311
Enrollment
1000
Registered
2020-10-09
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

Control Intervention1: Nil: Nil

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The donors who fulfil the eligibility criteria for platelet donation, as per SOP, will be included in study.

Exclusion criteria

Exclusion criteria: The donors who do not fulfil eligibility criteria for platelet donation, as per SOP, will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
To study immediate & delayed adverse events in plateletpheresis donors.Timepoint: The adverse events experienced by platelet donors will be analysed over a period of 4 months—

Secondary

MeasureTime frame
To analyze factors associated with these adverse events if any.Timepoint: It will be analysed over a period of 4 months—

Countries

India

Contacts

Public ContactDr Pallavi Gaikwad

Tata Memorial Hospital, HBNI

dr_priti99@yahoo.com9987815691

Outcome results

None listed

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