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Clinical Trials in Germany / NCT04083937
Recruiting Not applicable

Prostate Cancer Patients Treated With Alternative Radiation Oncology Strategies

NCT04083937 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2018-09-12
Last updated
2026-03-09

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

Hypofractionated radiotherapy with photonsHypofractionated radiotherapy with protonsNormofractionated radiotherapy with photons

Hypofractionated radiotherapy with photons: hypofractionated radiotherapy with photons (total dose 57.0 Gray in 19 fractions)

Hypofractionated radiotherapy with protons: hypofractionated radiotherapy with protons (total dose 57.0 Gray relative biological effectiveness (RBE) in 19 fractions)

Normofractionated radiotherapy with photons: normofractionated radiotherapy with photons (total dose 70.0 Gray in 35 fractions)

Study summary

As the most common male carcinoma, prostate cancer is a major tumor entity in oncology. In addition to definitive radiotherapy, surgical procedure is considered to be an oncologically equivalent therapeutic alternative for non-metastatic malignancies in the primary setting. However, a subsequent radiotherapy of the prostate bed is often necessary, which takes place as an "adjuvant" treatment immediately after surgery or in the course of a repeated increase in PSA and usually extends over several weeks. For the primary situation (without previous surgery), several randomized phase III clinical trials have shown that it is possible to shorten radiotherapy by increasing the single dose (called hypofractionation). In the context of two prospective Phase II studies, which were carried out in Heidelberg, it has since been shown that hypofractionation with both photons and protons is safe and feasible even in the postoperative situation.

The current, prospective and randomized PAROS study is now intended to demonstrate a multicentric phase III study as an improvement in the quality of life caused by rectum toxicity (primary endpoint) by the use of protons. The oncological non-inferiority of hypofractionated radiotherapy after surgery is a secondary endpoint.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * histology-proven prostate cancer with Gleason Score and PSA-value; * indication for prostate bed irradiation (adjuvant/ salvage) after prostatectomy; * Karnofsky-Index ≥ 70% * age ≥ 18 years Exclusion Criteria: * androgen deprivation therapy * lymphatic spread * macroscopic tumor/ R2 * stage IV (M1) * previous irradiation

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Heidelberg Heidelberg Germany Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04083937 on ClinicalTrials.gov ↗ ← All trials in Germany