Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06650033

Pelvis Adaptive Radiotherapy (ART)

Led by Royal North Shore Hospital · Updated on 2026-02-05

280

Participants Needed

1

Research Sites

320 weeks

Total Duration

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Sponsors

R

Royal North Shore Hospital

Lead Sponsor

N

Northern Sydney and Central Coast Area Health Service

Collaborating Sponsor

AI-Summary

What this Trial Is About

Pelvis Adaptive radiotherapy (ART) is a two phase study looking at using adaptive radiotherapy to help reduce toxicity for cancer patients having radiotherapy in the pelvic region. Adaptive radiotherapy is a new technology that provides the ability to account for daily changes in anatomy. Adaptive radiotherapy also provides a foundation for which radiotherapy margins might be safely reduced. Phase 1 of this study is looking to see if a radiation therapist centred adaptive workflow can be implemented. If phase 1 of this study is safe and feasible, the study will proceed to phase 2. Phase 2 of the study looks at using adaptive technology to reduce radiation treatment margins. The primary aim of this study is to see whether margin reduced treatment using adaptive radiotherapy can reduce side effects for patients with cancer in the pelvic area.

CONDITIONS

Official Title

Pelvis Adaptive Radiotherapy (ART)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18
  • ECOG performance status 0-2
  • Patients receiving curative or adjuvant pelvic radiation including prostate cancer with nodal treatment, post prostatectomy, bladder cancer, rectal cancer, anal cancer, adjuvant radiotherapy for gynecological cancers, or pelvic lymph nodes only
  • Ability to understand and willing to sign informed consent
Not Eligible

You will not qualify if you...

  • Presence of hip prosthesis
  • Patient separation from radiation center to skin edge > 24 cm measured on diagnostic scan

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

Northern Sydney Local Health District

St Leonards, New South Wales, Australia, 2065

Actively Recruiting

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Research Team

N

Nada Cheikh-Ali

CONTACT

H

Heidi Tsang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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