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Clinical Trial Summary

The goal is to gain insight in the development and course of the toxicity after a curative treatment of prostate cancer


Clinical Trial Description

All with curative intent treated prostate cancer patients will be enrolled in the SFP (Standard Follow-up Programme). It also includes the post -operative adjuvant treatments and the patients with positive lymph nodes. Patients will complete weekly questionnaires to score the patient -rated toxicity. Biweekly patients are seen by the treating radiation oncologist and / or AIOS in which the physician -rated toxicity is scored. In the follow-up will always patient -rated toxicity and physician -rated toxicity can be determined. Use of an SFP should yield a profit for the practitioner , such as the automatic generation of letters. This should apply to all SFPs . Quality of life and toxicity in patients will be completed on the touch-screen computers at FU visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03034187
Study type Observational
Source University Medical Center Groningen
Contact S. Aluwini, MD PhD
Phone +31503612346
Email s.al-uwini@umcg.nl
Status Recruiting
Phase
Start date April 1999
Completion date January 2028

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