Clinical Trials Directory

Trials / Completed

CompletedNCT00992251

Eligard Observational Registry for Patients With Prostate Cancer

A Prospective, Single Product, Observational Registry Involving Patients Presenting With Locally Advanced or Metastatic Prostate Cancer Receiving Eligard as Androgen Deprivation Treatment.

Status
Completed
Phase
Study type
Observational
Enrollment
354 (actual)
Sponsor
CMX Research · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this registry is to collect data on patient demographics, medical history, change in prostate, bone and overall health of the patients receiving androgen ablation treatment using Eligard. Data collected through this national registry program provides an opportunity to increase knowledge of efficacy and safety of the long term treatment with Eligard, provide a platform to better identify patient segments for the therapy with Eligard®. Furthermore registries are the only tools to accurately capture rare adverse events.

Detailed description

354 patients were enrolled in this study. Only 88 patients completed the study. For those patients completing the three years of data collection, 10% were considered Castrate Resistant and remained on Eligard®. For those patients not completing 3 years of follow-up, 8.8% were considered Castrate Resistant and did not continue in the study.

Conditions

Timeline

Start date
2009-08-01
Primary completion
2014-03-01
Completion
2014-03-01
First posted
2009-10-09
Last updated
2016-12-22

Locations

36 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00992251. Inclusion in this directory is not an endorsement.

Eligard Observational Registry for Patients With Prostate Cancer (NCT00992251) · Clinical Trials Directory