Collection and Distribution of Biospecimens for Novel Research Uses
iSpecimen Inc · NCT03848962
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 1 mo–89 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 10000
- US sites recruiting
- 1
- Study start
- June 30, 2016
- Record last updated
- November 9, 2022
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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").
Conditions: Cancer; Healthy; Gastrointestinal Complication; Autoimmune Diseases; Infectious Disease; Women's Health: High-Risk Pregnancy; Dermatologic Disease; Blood Disease
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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
Exclusion Criteria
- Subjects that do not meet the inclusion criteria outlined above.
Recruiting US locations
iSpecimen
Huntsville, AL 35801
Site contact: Emily L Hubbard · 256-797-0003 · ehubbard@ispecimen.com
Study contacts (from the official record)
- Emily L Hubbard · 2567970003 · ehubbard@ispecimen.com
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