Actively Recruiting

Age: 18Years +
All Genders
NCT05100342

Prospective Validation of a Points Score System Predicting 30-day Survival

Led by Indiana University · Updated on 2026-05-08

214

Participants Needed

3

Research Sites

272 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a one-stage single-arm phase II clinical trial designed to prospectively test the survival prediction tool as developed by Lee et al on patients referred to radiation oncology for palliative treatments. Survival prediction score based on objective data including laboratory values, attendance to emergency room, and primary cancer origin will be assigned to each patient at time of enrollment.

CONDITIONS

Official Title

Prospective Validation of a Points Score System Predicting 30-day Survival

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older at time of consent
  • Ability to provide written informed consent
  • Cancer diagnosis referred to Radiation Oncology for palliative radiation therapy
  • Patients who choose not to receive radiation therapy or are not recommended to receive it remain eligible
  • Patients do not need to complete prescribed palliative radiation therapy to remain eligible
Not Eligible

You will not qualify if you...

  • Unable to participate in follow-up visits as determined by the investigator (virtual or phone follow-up allowed)
  • Receiving definitive or curative radiation therapy
  • Self-reported pregnancy or nursing

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

IU Health West

Avon, Indiana, United States, 46123

Actively Recruiting

2

IU Health North / Schwarz Cancer Center

Carmel, Indiana, United States, 46032

Actively Recruiting

3

Methodist Hospital

Indianapolis, Indiana, United States, 46202

Actively Recruiting

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Research Team

J

Jessica Anders

CONTACT

N

Naoyuki G Saito, MD PhD

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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