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Evaluation of QoL, Tolerability and Use of Zoladex 10,8 SafeSystem for Advanced PCa - German IPEP Trial

This study has been completed.
Information provided by:
AstraZeneca Identifier:
First received: October 3, 2007
Last updated: October 4, 2007
Last verified: August 2007
Purpose of this study is the evaluation of QoL, tolerability and use of Zoladex 10,8 SafeSystem for advanced PCa under naturalistic conditions

Prostate Carcinoma

Study Type: Observational
Study Design: Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Prospective
Official Title: Quality Assurance Project in Patients With Advanced Prostate Carcinoma - Evaluation of Tolerability, Quality of Life and Usage of Zoladex 10,8 SafeSystem

Resource links provided by NLM:

Further study details as provided by AstraZeneca:

Enrollment: 1950
Study Start Date: June 2005

Ages Eligible for Study:   Child, Adult, Senior
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients with PCa, who will be treated with Zoladex 10,8 SafeSystem based on the current SPC
  Contacts and Locations
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Please refer to this study by its identifier: NCT00540059

Sponsors and Collaborators
Study Director: H Brasch AstraZeneca
  More Information Identifier: NCT00540059     History of Changes
Other Study ID Numbers: Zx-002 
Study First Received: October 3, 2007
Last Updated: October 4, 2007
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Keywords provided by AstraZeneca:
Prostate carcinoma

Additional relevant MeSH terms:
Prostatic Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Genital Neoplasms, Male
Urogenital Neoplasms
Neoplasms by Site
Genital Diseases, Male
Prostatic Diseases
Antineoplastic Agents, Hormonal
Antineoplastic Agents processed this record on October 21, 2016