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CompletedNCT01386684

Real Life Evaluation of Lupron in the Management of Prostate Cancer: A Canadian Post Marketing Observational Study

Canadian Real-Life Evaluation of the Effectiveness of Lupron in the Management of Prostate Cancer (CRONOS)

Status
Completed
Phase
Study type
Observational
Enrollment
552 (actual)
Sponsor
AbbVie (prior sponsor, Abbott) · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the Canadian Real Life Evaluation of the Effectiveness of Lupron in the Management of Prostate Cancer.

Detailed description

This is a Canadian Post Marketing Observational Study utilizing a prospective cohort design. Patients with Prostate Cancer who are prescribed Lupron will be entered into the study cohort and will be followed for a maximum of 36 months with recommended assessments at 3, 6, 12, 18, 24, 30 and 36 months after baseline. Treatment of the patients and follow up will be according to the physician's judgment, regional regulations and the product monograph.

Conditions

Timeline

Start date
2011-06-28
Primary completion
2016-09-08
Completion
2016-09-08
First posted
2011-07-01
Last updated
2018-12-13
Results posted
2018-04-02

Source: ClinicalTrials.gov record NCT01386684. Inclusion in this directory is not an endorsement.

Real Life Evaluation of Lupron in the Management of Prostate Cancer: A Canadian Post Marketing Observational Study (NCT01386684) · Clinical Trials Directory