Healthy Clinical Trial
— M-PRPOfficial title:
A Single Center, Prospective Study to Compare the Quality and Quantity of the Cellular Content of M-PRP Harvested After Peripheral Mobilization of Progenitor Cells Using Filgrastim Versus Pegfilgrastim
NCT number | NCT05573386 |
Other study ID # | MPRP |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | August 9, 2021 |
Est. completion date | August 5, 2023 |
The goal of this prospective, observational study is to compare the quality and quantity of the cellular content of platelet-rich plasma harvested after administering one of two cell-stimulating proteins, filgrastim and pegfilgrastim. The main question it aims to answer is: • Will participants have a similar cellular content when comparing a 4-day filgrastim treatment to a one-day pegfilgrastim treatment? Participants will have the following intervention administered: - 130mL of blood will be drawn on the first visit after consent and in followup visits after administering treatment (4 days for filgrastim, 7 days for pegfilgrastim) - Half of all participants will receive filgrastim first, followed by pegfilgrastim 8 weeks after filgrastim treatment concludes. The other half will receive the treatments in reverse order Researchers will compare the quality and quantity of cell content after each treatment administration as well as comparing differences in data dependent on which order treatment was given.
Status | Recruiting |
Enrollment | 10 |
Est. completion date | August 5, 2023 |
Est. primary completion date | August 5, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 19 Years to 39 Years |
Eligibility | Inclusion Criteria: - Healthy 19-39 of age and weight 50-100kg - Subject consents to coming 5 serial days for filgrastim treatment and additional blood draw, 8 weeks later two additional visits for pegfilgrastim treatment and blood draw 7 days later. This order of administration will be provided to half of the participants, where as the other half will receive the same treatments in reverse order. Exclusion Criteria: - Female - Weight < 50kg or > 100kg - Previous allergic reaction to filgrastim, PEG, lidocaine, latex, acrylic, or any other injectable numbing agent - History of Diabetes - Abdominal tenderness to palpation - Unclear lung fields on physical exam - Splenomegaly - Significant cardiovascular, renal, hepatic, or pulmonary disease - White blood cell count (WBC) over 20,000/microliter (mcL) upon initial complete blood count (CBC) screening - Blood disorders, autoimmune disorders, disorders requiring immunosuppression, cancer, an ongoing infectious disease, sickle cell, or other blood disorders. |
Country | Name | City | State |
---|---|---|---|
United States | Andrews Research and Education Foundation | Gulf Breeze | Florida |
Lead Sponsor | Collaborator |
---|---|
Andrews Research & Education Foundation | Florida |
United States,
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* Note: There are 50 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Arthrex Angel system for PRP concentration | Machine utilizing centrifugation and optics to precisely separate cell types using buffy coat method. . All cells have a density range and non-uniformly after centrifugation. Arthrex Angel system has the unique ability to isolate specific cells using inherent properties of cells that absorb differing wavelengths of light. The settings on the system can be controlled to adjust the proportion of cells versus plasma. Increasing the setting from 7% to 15%, the Angel system isolates more cells from a deeper portion of the buffy coat, which results in capturing more HPCs per volume. | at time of enrollment | |
Primary | Arthrex Angel system for PRP concentration | Machine utilizing centrifugation and optics to precisely separate cell types using buffy coat method. . All cells have a density range and non-uniformly after centrifugation. Arthrex Angel system has the unique ability to isolate specific cells using inherent properties of cells that absorb differing wavelengths of light. The settings on the system can be controlled to adjust the proportion of cells versus plasma. Increasing the setting from 7% to 15%, the Angel system isolates more cells from a deeper portion of the buffy coat, which results in capturing more HPCs per volume. | 8 weeks from enrollment, upon switch in treatment from filgrastim/pegfilgrastim |
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