Evaluation of QoL, Tolerability and Use of Zoladex 10,8 SafeSystem for Advanced PCa - German IPEP Trial
This study has been completed.
Sponsor:
AstraZeneca
Information provided by:
AstraZeneca
ClinicalTrials.gov Identifier:
NCT00540059
First received: October 3, 2007
Last updated: October 4, 2007
Last verified: August 2007
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Purpose
Purpose of this study is the evaluation of QoL, tolerability and use of Zoladex 10,8 SafeSystem for advanced PCa under naturalistic conditions
| Condition |
|---|
|
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:
Eligibility| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patients with PCa, who will be treated with Zoladex 10,8 SafeSystem based on the current SPC
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov 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 LHRH Zoladex |
Additional relevant MeSH terms:
|
Carcinoma Prostatic Neoplasms Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site |
Genital Diseases, Male Prostatic Diseases Goserelin Antineoplastic Agents, Hormonal Antineoplastic Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013