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ACTIVE NOT RECRUITING
NCT01550237
NA

Curative Image Guided Radiotherapy for Prostate Cancer

Sponsor: St. Olavs Hospital

View on ClinicalTrials.gov

Summary

The clinical importance of cone beam computer tomography based image guided radiotherapy (CT- IGRT) has not been established. The primary aim of the present trial is to investigate whether CT- IGRT and consequently reduced safety margins reduces the rectal side effects from curative, high dose radiotherapy in prostate cancer. Any impact of the reduced planning target volume in the CT- IGRT arm on biochemical freedom from disease will be evaluated as secondary outcome. An open randomised phase III trial. The included men will be randomised to receive curative radiotherapy to 78 Gy in 39 fractions with weekly orthogonal position verification and standard safety margins (10-15 mm) or 78 Gy in 39 fractions with daily CT position verification and reduced safety margins (7mm).

Official title: A Randomised, Two Centre Trial on Daily Cone-beam vs Standard Weekly Orthogonal Image Guided Radiotherapy (IGRT) for Prostate Cancer

Key Details

Gender

MALE

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

260

Start Date

2012-10

Completion Date

2025-09

Last Updated

2025-06-05

Healthy Volunteers

No

Interventions

RADIATION

radiotherapy daily verification reduced safety margins

curative radiotherapy to 78 Gy in 39 fractions with daily CT position verification and reduced safety margins (7mm)

RADIATION

radiotherapy weekly verification standard safety margins

curative radiotherapy to 78 Gy in 39 fractions with weekly orthogonal position verification and standard safety margins (10-15 mm)

Locations (2)

Ålesund Sykehus

Ålesund, Norway

St Olavs Hospital

Trondheim, Norway