Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT06778408

Hybrid Arc Palliative Radiation Therapy (HART): A Single Arm Phase II Trial

Led by University of Vermont Medical Center · Updated on 2026-02-05

103

Participants Needed

1

Research Sites

148 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a prospective single-center single-arm Phase II trial of HART for patients with metastatic cancer. The primary objective is to assess the incidence of acute GI toxicity following HART. PRO-CTCAE GI scores observed in the study patients will be compared to historical rates. Secondary outcomes include measuring changes in health-related quality of life, esophageal quality of life, toxicity, dosimetric outcomes, and pain.

CONDITIONS

Official Title

Hybrid Arc Palliative Radiation Therapy (HART): A Single Arm Phase II Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histological confirmation of cancer with radiographic (CT, MRI or PET) evidence of metastatic disease
  • Palliative radiotherapy indicated for bone or soft tissue metastases or primary targets in the thorax, abdomen, or pelvis as part of standard care
  • Age 18 years or older
  • Women of child-bearing potential and men must agree to use effective contraception during the study and for 90 days after therapy
  • Ability to understand and willingness to sign informed consent
Not Eligible

You will not qualify if you...

  • Receiving any other investigational agents or concurrent cytotoxic chemotherapy
  • Pregnant or nursing women
  • Serious medical conditions that prevent safe delivery of radiation therapy as determined by the radiation oncologist

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Vermont Medical Center

Burlington, Vermont, United States, 05401

Actively Recruiting

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Research Team

N

Nataniel H Lester-Coll, MD

CONTACT

C

Christopher Anker, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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