Actively Recruiting

Age: 18Years +
MALE
NCT05840484

Comprehensive Monitoring of Men With Prostate Cancer Cared for by "Active Surveillance

Led by M.D. Anderson Cancer Center · Updated on 2026-02-19

100

Participants Needed

1

Research Sites

330 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Prostate cancer is the most commonly diagnosed cancer in men. However, there is a wide range in prognosis determined by a host of factors. This study will evaluate the feasibility of guiding therapeutic intervention electronically facilitated symptom and disease monitoring in patients being followed on Active Surveillance. Additionally, we will develop a tissue and data resource to support discovery and hypothesis generation to evaluate germline and/or somatic alterations in relation to cancer-specific and overall outcomes..

CONDITIONS

Official Title

Comprehensive Monitoring of Men With Prostate Cancer Cared for by "Active Surveillance

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologic diagnosis of prostate adenocarcinoma within 24 months of study entry
  • Meets one of the following: very low or low-risk prostate cancer per NCCN guidelines, intermediate-risk prostate cancer requesting active surveillance, or high-risk localized prostate cancer with severe medical comorbidities
  • Agree to comply with the surveillance schedule
  • Age over 18 years
  • Written informed consent provided
  • Fluent in English to participate in symptom and patient report monitoring
Not Eligible

You will not qualify if you...

  • Decline to share medical data for research purposes
  • Prior radiation therapy for treatment of the primary tumor
  • Planned hormonal therapy, chemotherapy, or radiation therapy while on the study protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

C

Christopher Logothetis, 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

3

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