Actively Recruiting

Age: 18Years +
All Genders
NCT06081517

Evaluating Disparities in Precision Oncology

Led by Indiana University · Updated on 2025-06-13

10600

Participants Needed

1

Research Sites

253 weeks

Total Duration

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AI-Summary

What this Trial Is About

This is a non-randomized observational trial designed to collect detailed clinical, social determinant, and genomic data from patients enrolled in molecular oncology tumor boards across four comprehensive cancer centers.

CONDITIONS

Official Title

Evaluating Disparities in Precision Oncology

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to provide written informed consent and HIPAA authorization
  • Patients must be �3E= 18 years old at the time of consent
  • Patients planning to undergo molecular testing as part of their routine cancer care
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Indiana University Health Melvin and Bren Simon Comprehensive Cancer Center

Indianapolis, Indiana, United States, 46202

Actively Recruiting

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Research Team

M

Maria McQuade, BA

CONTACT

B

Bryan P Schneider, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Evaluating Disparities in Precision Oncology | DecenTrialz