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Tissue Repository Providing Annotated Biospecimens for Approved Investigator-directed Biomedical Research Initiatives

Tissue Repository Providing Annotated Biospecimens for Approved Investigator-directed Biomedical Research Initiatives

Recruiting
18-85 years
All
Phase N/A

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Overview

To collect, preserve, and/or distribute annotated biospecimens and associated medical data to institutionally approved, investigator-directed biomedical research to discover and develop new treatments, diagnostics, and preventative methods for specific and complex conditions.

Eligibility

Inclusion Criteria:

  • Persons 18 to 85 years of age at the date of informed consent.
  • If presenting with a history of a specific condition, the diagnosis is confirmable in the medical record or may be confirmed using other forms of verification including self-reporting.
  • Understands the procedures and requirements of the study by providing written informed consent (or verbal assent if a legally authorized representative will sign the ICF), including consent for authorization for protected health information disclosure.

Exclusion Criteria:

  • Persons younger than 18 years of age or older than 85 years of age at the date of informed consent.
  • Receipt of blood products 30 days before the study blood draw.
  • Receipt of an investigational (unapproved) drug 30 days before the study blood draw.
  • A confirmable diagnosis of any medical condition that would increase potential phlebotomy risks.
  • Has donated a unit of blood within the last 2 months at the date of informed consent.

Study details
    Age-Related Macular Degeneration
    Allergies
    Alpha-Gal Syndrome
    Alzheimer Disease
    Amyloidosis
    Ankylosing Spondylitis
    Arthritis
    Alopecia Areata
    Asthma
    Atopic Dermatitis
    Autism
    Autoimmune Hepatitis
    Behcet's Disease
    Beta-Thalassemia
    Cancer
    Celiac Disease
    Kidney Diseases
    COPD
    Crohn Disease
    Cystic Fibrosis
    Diabetes
    Dravet Syndrome
    DMD
    Fibromyalgia
    Graves Disease
    Thyroid Diseases
    Hepatitis
    Hidradenitis Suppurativa
    ITP
    Leukemia
    ALS
    Lupus or SLE
    Lymphoma
    Multiple Sclerosis
    Myasthenia Gravis
    Heart Diseases
    Parkinson Disease
    Pemphigus Vulgaris
    Cirrhosis
    Psoriasis
    Schizophrenia
    Scleroderma
    Sickle Cell Disease
    Stroke
    Ulcerative Colitis
    Vasculitis
    Vitiligo

NCT05635266

Sanguine Biosciences

18 May 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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