RECRUITING

NIEHS Repository of Stored Biological Samples for Future Use

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Background: Laboratory tests that use blood and urine can provide a great deal of information about human health and disease. To develop even better tests and to improve the ways samples are handled for testing researchers need to experiment with samples from healthy people. Objective: This natural history study will collect blood and urine from healthy people. The samples will build a repository that will be used for all kinds of research. Eligibility: Healthy people aged 18 years or older. Design: Participants will have 1 study visit. The visit will last up to 2 hours. Participants will be screened. They will answer questions about their health history. They will list any medications they take. They will consent to donate samples for research and future use: Blood: Up to 4.5 tablespoons of blood may be collected from a needle inserted into a vein. Urine: Participants will be given a sterile container to provide a sample. Some participants may be asked to provide other types of samples. Some participants may be asked to provide new samples if their first ones are depleted.

Official Title

NIEHS Repository of Stored Biological Samples for Future Use

Quick Facts

Study Start:2024-07-15
Study Completion:2032-07-19
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05666739

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Stated willingness to comply with all study procedures and availability for the duration of the study.
  2. 2. Ability to provide informed consent.
  3. 3. Male or female, aged \>=18
  4. 4. Able to travel to the NIEHS CRU for study visits
  1. 1. Not willing to have samples stored for future use.
  2. 2. Any condition that, in the investigator s opinion, places the participant at undue risk for complications associated with required study procedures.

Contacts and Locations

Study Contact

NIEHS Join A Study Recruitment Group
CONTACT
(855) 696-4347
myniehs@nih.gov
Stavros Garantziotis, M.D.
CONTACT
(984) 287-4412
garantziotis@mail.nih.gov

Principal Investigator

Stavros Garantziotis, M.D.
PRINCIPAL_INVESTIGATOR
National Institute of Environmental Health Sciences (NIEHS)

Study Locations (Sites)

NIEHS Clinical Research Unit (CRU)
Research Triangle Park, North Carolina, 27709
United States

Collaborators and Investigators

Sponsor: National Institute of Environmental Health Sciences (NIEHS)

  • Stavros Garantziotis, M.D., PRINCIPAL_INVESTIGATOR, National Institute of Environmental Health Sciences (NIEHS)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-15
Study Completion Date2032-07-19

Study Record Updates

Study Start Date2024-07-15
Study Completion Date2032-07-19

Terms related to this study

Keywords Provided by Researchers

  • Blood
  • Urine
  • Assay Development
  • Natural History

Additional Relevant MeSH Terms

  • Normal Physiology