- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06151977
Impact of Lecuofiltration of Packed Red Blood Cells on Different Hematological Parameters Measured by Advia 2120
November 21, 2023 updated by: Yasmin Mohamed Sayed, Assiut University
Parameters of lecuofiltration of packed Red blood cells.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
Impact of lecuofiltration of packed Red blood cells on different hematological parameters measured by Advia 2120
Study Type
Observational
Enrollment (Estimated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yasmin Mo Sayed, Res
- Phone Number: 01155456741
- Email: yasmeend4@gmail.com
Study Contact Backup
- Name: Saher Ab Elgamal, Pro
- Phone Number: 01002342312
- Email: S.elgammal@med.aun.edu.eg
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Healthy donors
Description
Inclusion Criteria:
packed RBC ADIA2120
Exclusion Criteria:
- Whole blood
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Impact of lecuofiltration of packed Red blood cells on different hematological parameters measured by Advia 2120
Time Frame: From 1/1/ 2024 to 29/12/2024
|
Leucodepletion of packed RBC affects the different parameters of blood component as hemoglobin, platelets , WBCs and so on.
Measurement will be done by ADIA2120 hematological analyzer by taking a sample from the packed RBC before and after leucodepletion to compare the difference in hematological parameters.
|
From 1/1/ 2024 to 29/12/2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 1, 2024
Primary Completion (Estimated)
December 29, 2024
Study Completion (Estimated)
December 29, 2024
Study Registration Dates
First Submitted
November 16, 2023
First Submitted That Met QC Criteria
November 21, 2023
First Posted (Actual)
November 30, 2023
Study Record Updates
Last Update Posted (Actual)
November 30, 2023
Last Update Submitted That Met QC Criteria
November 21, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Leucodepleted blood parameters
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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