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Research Report
Platelet-Rich Plasma: A Comprehensive Analysis of its Composition, Mechanisms, and Clinical Utility in Regenerative Medicine
I. Introduction to Platelet-Rich Plasma (PRP)
A. Definition and Core Concept
Platelet-Rich Plasma (PRP) is an autologous biological product derived from a patient's own whole blood. It represents a processed liquid fraction of peripheral blood characterized by a platelet concentration significantly above baseline physiological levels.[1] Normal human blood typically contains approximately 150,000 to 350,000 platelets per microliter. In contrast, therapeutic PRP preparations are generally designed to achieve platelet concentrations that are 3 to 5 times higher than this baseline, often aiming for or exceeding 1 million platelets per microliter.[3] Some advanced preparation systems report the capability to achieve even greater concentration factors, potentially up to 9-fold or 11-fold increases.[3]
This concentration of platelets results in a product rich in a diverse array of growth factors, cytokines, chemokines, and other bioactive molecules. These components are integral to the body's natural processes of tissue repair and regeneration.[1] The fundamental therapeutic rationale for utilizing PRP is to leverage and amplify these endogenous healing mechanisms. By delivering a supraphysiological dose of these reparative biomolecules directly to a site of injury, chronic degeneration, or surgical intervention, PRP aims to accelerate and enhance the natural healing cascade, potentially leading to improved clinical outcomes.[1]
B. Historical Background and Evolution
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/03/26 | Phase 1 | Recruiting | Tang-Du Hospital | ||
2024/11/15 | Phase 2 | Not yet recruiting | |||
2022/10/18 | Not Applicable | Completed | Hebei Medical University Third Hospital | ||
2022/01/31 | Phase 2 | ENROLLING_BY_INVITATION | Wroclaw Medical University | ||
2021/11/03 | Not Applicable | Completed | |||
2020/12/09 | Phase 1 | UNKNOWN | |||
2020/02/11 | Not Applicable | Completed | Yung-Tsan Wu | ||
2017/07/07 | Phase 4 | Completed | |||
2016/10/12 | Phase 3 | Completed | |||
2014/08/12 | Phase 3 | Withdrawn | Basque Health Service |
FDA Drug Approvals
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No FDA approvals found for this drug. |
EMA Drug Approvals
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No EMA approvals found for this drug. |
HSA Drug Approvals
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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No TGA approvals found for this drug. |
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