Collection and Distribution of Biospecimens for Novel Research

Status unconfirmed

Conditions studied: Cancer, Healthy, Gastrointestinal Complication, Autoimmune Diseases, Infectious Disease, Women's Health: High-Risk Pregnancy, Dermatologic Disease, Blood Disease

In brief

iSpecimen aims to create a clinical partner network of hospitals, laboratories, academic institutions, and other healthcare organizations ("institutions") capable of providing researchers and educators ("researchers") with annotated biospecimens for use in biomarker discovery and validation; diagnostic test and instrumentation development and validation; therapeutics development; other medical research including the impact that various specimen collection and handling methods and conditions have on research results; and in education such as researcher or physician training (collectively "research").

Key facts

Study ID

NCT05080907

Run by

iSpecimen Inc

People needed

100000

Starts

2016-07-15

Expected to finish

2025-01-01

Last updated by the study team

2022-11-09

Who can join

Age: 1 and older, up to 99. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Individual is developmentally aged 7 years old and above for RUO collections (only)
• Individual meets requirements of a current request for research materials from iSpecimen
• If a blood collection will be performed as part of the screening process or RUO collection, the individual's health will be assessed by medical staff through medical record review, clinical exam, and/or the review of an updated medical history as provided by the participant
• Individual has reviewed and signed a consent form for an RUO specimen collection if required as part of the research or if a minor or a person with diminished decision-making capacity, their parent/guardian or Legally Authorized - Representative has reviewed and signed the consent form on their behalf.
• Individual has reviewed and signed a consent form for remnant specimen usage in research if required as part of the research or if a minor or a person with diminished decision-making capacity, their parent/guardian or Legally Authorized Representative has reviewed and signed the consent form on their behalf

You may not qualify if…

• Subjects that do not meet the inclusion criteria outlined above.

Where it is running

• Central Alabama — Birmingham, Alabama, United States
• Northern Alabama — Huntsville, Alabama, United States
• Southern Alabama Area — Mobile, Alabama, United States
• Central Alabama — Montgomery, Alabama, United States
• Western New York — Buffalo, New York, United States
• Greater Philadelphia Area — Philadelphia, Pennsylvania, United States
• Western Pennsylvania — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.