CClinicalTrials.gg
CompletedNCT00220194Updated Oct 14, 2016

A Six-Month, Open-Label, Crossover Study Of the Maintenance Of Serum Testosterone And PSA Suppression After Switching Between Lupron 22.5 Mg And Eligard 22.5 Mg Or Zoladex 10.8 Mg And Eligard 22.5 Mg In Patients With Advanced Prostate Cancer

A Phase 4 interventional study of leuprolide acetate in Cancer of Prostate, sponsored by San Bernardino Urological Associates Medical Group Inc. Completed at 1 site in United States. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-10-14.

Sponsored by San Bernardino Urological Associates Medical Group Inc · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years and older
Sex
Male
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Study summary

Comparing the effect of switching from Lupron and Zoladex to Eligard. PSA and Testosterone levels are measured at set intervals to determine if Eligard is equal or better then Lupron or Zoladex in advanced Prostate Cancer patients.

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Conditions studied

  • Cancer of Prostate

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03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's enrollment of 100 is above the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

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Lead sponsor

This is the only study on the registry with San Bernardino Urological Associates Medical Group Inc as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria: Patient with Advanced Ca, on stable dose of Lupron or Zoladex

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Exclusion Criteria:

  • Previous exposure to Eligard.
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
100 participants

Interventions

  • Drugleuprolide acetate
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Study locations

1 site
  • San bernardino Urological Associates Medical Group
    San Bernardino, California 92404, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 14, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00220194
Lead sponsor
San Bernardino Urological Associates Medical Group Inc
First posted
Sep 22, 2005
Start date
Apr 2003
Completion
Jun 2005
Last update
Oct 14, 2016

Study contacts

Franklin M Chu, MD
principal investigator · San Bernfardino Urological Associates
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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