Program for Collection of BioSpecimens

About this Study

The objective of the protocol is to conduct biospecimen collection while protectingthe rights, privacy, and safety of those subjects who provide biospecimens to assist in, but not limited to, the evaluation of current products, products in development and/or competitive products, for device assessment studies, marketing purposes,design control testing, quality control, product incident reports, post-marketrequirements, training, and clinical trial testing for product performance testing.

Sponsor Protocol ID:pending
IRB Number:pending
Pending Activation
Observational/Not Applicable
October 09, 2020
Eligibility Criteria
Both Male and Female

Inclusion Criteria

Subjects that satisfy all of the following conditions will be considered for participation:

a.         Meet the minimum state and site age                                requirements.

b.          Able to read, write and follow instructions in                   English or the language of Informed Consent                   Form  

c.         Able and willing to provide informed consent

Exclusion Criteria

Subjects with any one of the following characteristics will be excluded from participation in this study:

a.     Medical condition that would put them at risk for donating. This may include, but is not limited to, such conditions as, peptic ulcer disease, gastrointestinal problems, anemia, cancer, heart/lung/liver disease, malaria, chest pains, planned or recent surgical procedure, syphilis, tuberculosis, clotting disorders.

b.     Have any known adverse reaction to sample donations or blood drawing procedures, such as allergies, uncontrolled bleeding, recurrent fainting or convulsions.

c.     For sample collection with Broom or Brush/Spatula: Known to be pregnant.

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Emergency Medicine
Participating Locations
University Hospital
Contact Information
Contact Name: Rebekah Peacock
Phone Number: 601-815-3008
Principal Investigator:Galbraith, James W, M.D.
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