RECRUITING

The Use of Residual De-identified Specimens and/or Samples From Patients for Clinical Research

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

Acquire residual human specimens and/or samples from patient samples which were sent for testing at LabPMM, LLC for Clinical Research

Official Title

The Use of Residual De-identified Specimens and/or Samples From Patients for Clinical Research

Quick Facts

Study Start:2024-03-30
Study Completion:2027-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06222164

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Specimen/sample, peripheral blood (PB), bone marrow (BM), genomic DNA (gDNA) and/or formalin-fixed paraffin-embedded tissue (FFPE) from patients whose specimens/samples have been sent to LabPMM for clinical testing
  2. 2. Donor Age ≥ 18 years
  1. 1. Sample/specimen has been obtained from a third-party vendor with a Materials Transfer Agreement (MTA) on file with LabPMM
  2. 2. The specimens/samples have previously been enrolled in a clinical study

Contacts and Locations

Study Contact

Andrew Schut
CONTACT
+1 858.224.6600
aschut@invivoscribe.com

Study Locations (Sites)

LabPMM
San Diego, California, 92121
United States

Collaborators and Investigators

Sponsor: Invivoscribe, Inc.

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 Date2024-03-30
Study Completion Date2027-06-30

Study Record Updates

Study Start Date2024-03-30
Study Completion Date2027-06-30

Terms related to this study

Keywords Provided by Researchers

  • residual samples hematologic diseases

Additional Relevant MeSH Terms

  • Hematologic Diseases