NCT00523484CompletedNot Applicable
An Observational Study to Assess Correlation Between Prostate Specific Antigen & Beck Anxiety Index in Prostate Cancer Patients Under Hormonal Therapy
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- AstraZeneca
- Enrollment
- 1,200
- Locations
- 1
Study Overview
Brief Summary
This study is an observational study to see whether anxiety level can be correlated with PSA level under the current practice in the patients of prostate cancer taking hormonal therapy. For assessment of anxiety level BAI(Beck Anxiety Inventory) will be used. The target population for this study is the patients of prostate cancer diagnosed previously and who are taking hormonal therapy with regular follow-up and PSA test. The follow-up duration will be total 6 months with interim visit at 3 month and final visit at 6 month.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Male
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Provision of written informed consent
- •Patients who take PSA test regularly
- •Observation suitable patients for PSA change according to hormonal treatment at least for 6months
- •Locally advanced or advanced prostate cancer patients who is suitable for hormonal therapy
- •Prostate Cancer Patients who has been taking one treatment among 3 hormonal therapies in below:
- •Bicalutamide Monotherapy : Bicalutamide 150mg/day
- •Goserelin 3.6mg/10.8mg
- •MAB(Maximal Androgen Blockade) :Bicalutamide 50mg + Goserelin 3.6/10.8mg
Exclusion Criteria
- •Prohibition use under permitted indication
- •Previous inclusion in the present study
- •Participation in a clinical study during the last 30 days
Investigators
Study Sites (1)
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