ACP Max Cellular Characterization At 90 ML Starting Volume

Overview

About this study

The aims of this study are to comprehensively characterize the cellular composition of PRP from ACP Max; quantify relevant cell types in PRP.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

To be eligible for inclusion in this study, the subjects must meet any of the following criteria:

  • Subjects, 18 years and older, undergoing routine orthopedic surgical procedures that will have already have IV placement as part of the surgical procedure.

  • Complete a signed consent form.

Exclusion Criteria: 

To be eligible for inclusion in this study, the subjects must not meet any of the following criteria:

  • History of superficial infection within 6 months of study enrollment, or  evidence of current superficial infection.

  • Taking anticoagulant medications (e.g. warfarin, heparin) or clopidogrel (Plavix).

  • Taking anti-rheumatic disease medication (including methotrexate or other antimetabolites) within 3 months prior to study enrollment.

  • On chronic, immunosuppressive transplant therapy or having a chronic, immunosuppressive state, including use of systemic steroids/corticosteroids.

  • Systemicinflammatory,rheumatologicalorconnectivetissuedisorderincludingbutnot limited to rheumatoid arthritis, systemic sclerosis, system lupus erythematosus, and Ehlers-Danlos Syndrome.

  • Ongoing infectious disease, including but not limited to tuberculosis, HIV, hepatitis, and syphilis.

  • History of cancer/malignancy with the exception of adequately treated basal cell or squamous cell carcinoma of the skin within the last 5 years.

  • History of blood dyscrasia, including but not limited to anemia, thrombocytopenia, and monoclonal gammopathy.

  • Currently pregnant individuals.

  • Individuals under the age of 18 years old.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 10/24/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Edward Haupt

Open for enrollment

Contact information:

Edward Haupt

(904) 953-2496

haupt.edward@mayo.edu

More information

Publications

Publications are currently not available