Understanding toxicity in prostate cancer treatment

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to gather insights into the development and progression of toxicity experienced by patients after curative treatment for prostate cancer. Participants will be enrolled in a Standard Follow-up Programme (SFP) and will complete weekly questionnaires to assess patient-rated toxicity. Additionally, biweekly evaluations by radiation oncologists will provide physician-rated toxicity scores. The study focuses on both acute and late toxicity, as well as the impact on quality of life for these patients.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* All curative treated patients with prostatecancer( with positive lymph nodes)
* All patients who will be treated with RT( including post-operative, adjuvant treatments)
* Are willing to fill in toxicity and QOL-questionnarys (QLQ-PR25 en de QLQ-C30)

Exclusion Criteria:

Patients who are not willing to fill in toxicity and QOL-questionnarys Patients who will not get RT Non-curative or palliative treated patients (with bone mestasis) Non-prostate cancer-patients

Where it's running

• University Medical Center Groningen
  Groningen, Netherlands Recruiting

Study contacts

• Study coordinator: S. Aluwini, MD PhD
• Email: s.al-uwini@umcg.nl
• Phone: +31503612346

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.