Non-Interventional Study PREVENT - PREVENT

Study identifier:NIS-ORU-XXX-2014/2

ClinicalTrials.gov identifier:NCT02155998

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Non-interventional Study of Postoperative or post-Radiation trEatment habits in locally adVanced prostate cancer patiENTs (high risk)- PREVENT

Medical condition

postoperative or postradiation adjuvant androgen deprivation therapy in locally advanced prostate cancer (high and very high risk) patients

Phase

N/A

Healthy volunteers

No

Study drug

-

Sex

Male

Actual Enrollment

200

Study type

Observational

Age

N/A

Date

Study Start Date: 16 Jul 2014
Primary Completion Date: 14 Dec 2016
Study Completion Date: 14 Dec 2016

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Apr 2019 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria