Skip to content

Comparison of Pooled Platelets and Single Donor Platelet Concentrate

In Vitro and In Vivo Comparison of Buffy Coat Pooled Platelets and Apheresis Platelet Concentrate in Hemato-Oncology Patients in a Tertiary Care Centre: A Non-Randomized Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/047874
Enrollment
35
Registered
2022-12-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: C910- Acute lymphoblastic leukemia [ALL] Health Condition 2: C920- Acute myeloblastic leukemia Health Condition 3: C925- Acute myelomonocytic leukemia Health Condition 4: C924- Acute promyelocytic leukemia Health Condition 5: C919- Lymphoid leukemia, unspecified Health Condition 6: C929- Myeloid leukemia, unspecified Health Condition 7: C91Z- Other lymphoid leukemia Health Condition 8: C92Z- Other myeloid leukemia Health Condition 9: C96Z- Other specified malignant neoplasms

Interventions

Intervention1: Buffy Coat Pooled Platelets: 1 unit (200-300ml) of Buffy Coat Pooled Platelets will be transfused intravenously to hemato-oncology patients with thrombocytopenia. The platelet increment

Sponsors

Dr Juhi Bhatia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All hemato-oncology patients admitted to the Department of Medical Oncology-Hematology, AIIMS Rishikesh, who will be requiring more than one adult dose of platelet transfusion during their single admission at AIIMS Rishikesh.

Exclusion criteria

Exclusion criteria: 1. Patients requiring less than 2 adult doses of platelet transfusion during the course of their single admission at AIIMS Rishikesh. 2. Patients not willing to be a part of the study. 3. Patients requiring multiple transfusions of random donor platelets but requiring less than one adult dose of platelet concentrate during the course of a single admission.

Design outcomes

Primary

MeasureTime frame
1. Increment in platelet count in patients with buffy coat pooled platelets and apheresis platelet concentrate transfusion 2. Analysis of the transfusion reactions after transfusion of both the productsTimepoint: 1 hour and 24 hours post transfusion

Secondary

MeasureTime frame
Analysis of the in vitro quality parameters of buffy coat pooled platelet concentrate and apheresis platelet concentrateTimepoint: Day 1 and Day 5

Countries

India

Contacts

Public ContactDr Juhi Bhatia

AIIMS Rishikesh

ashish.jain.modi@gmail.com9917817515

Outcome results

None listed

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