Evaluating the Impact of Early Versus Delayed 5 Alpha Reductase Inhibitor Treatment on the Risk of Emergent Surgery in Men With Benign Prostatic Hyperplasia
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| ClinicalTrials.gov Identifier: NCT01332487 |
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Recruitment Status :
Completed
First Posted : April 11, 2011
Results First Posted : February 29, 2012
Last Update Posted : June 19, 2017
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| Condition or disease | Intervention/treatment |
|---|---|
| Prostatic Hyperplasia | Drug: 5ARI + AB |
| Study Type : | Observational |
| Actual Enrollment : | 4068 participants |
| Observational Model: | Cohort |
| Time Perspective: | Retrospective |
| Official Title: | Evaluating the Impact of Early Versus Delayed 5 Alpha Reductase Inhibitor Treatment on the Risk of Emergent Surgery in Men With Benign Prostatic Hyperplasia |
| Study Start Date : | August 2010 |
| Actual Primary Completion Date : | August 2010 |
| Actual Study Completion Date : | August 2010 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Early initiation of 5ARI therapy
Patients starting 5ARI therapy within 30 days of initiating AB therapy
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Drug: 5ARI + AB
5ARI: Dutasteride or Finasteride and any AB: Doxazosin, Prazosin, Tamsulosin, Terazosin or Alfuzosin |
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Delayed initiation of 5ARI therapy
Patients starting 5ARI therapy more than 30 days but less than 6 months from the initiation of AB therapy
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Drug: 5ARI + AB
5ARI: Dutasteride or Finasteride and any AB: Doxazosin, Prazosin, Tamsulosin, Terazosin or Alfuzosin |
- Number of Participants Who Experienced Progression of Disease [ Time Frame: Up to 5 months ]The number of participants in each study group with a treatment code for acute urinary retention, surgery, or emergency surgery (defined as surgery within 30 days following a diagnosis of acute urinary retention) was measured.
- Number of Participants With the Indicated Time Between Acute Urinary Retention and Subsequent Surgery [ Time Frame: 6 months ]
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| Ages Eligible for Study: | 50 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- Male
- aged 50 years or older
- diagnostic claim for BPH
- prescription claim for an AB and a 5ARI in the observation period (5ARI must occur within a 6-month window after the AB).
- continuously eligible for 6 months prior to and 12 months after index prescription date
Exclusion Criteria:
- prostate or bladder cancer during the study period
- any prostate-related surgical procedure within 5 months of the index prescription date
- prescription claim for finasteride 1 mg for male pattern baldness during the study period
- 5ARI therapy prior to initiation of AB therapy
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01332487
| Study Director: | GSK Clinical Trials | GlaxoSmithKline |
| Responsible Party: | GlaxoSmithKline |
| ClinicalTrials.gov Identifier: | NCT01332487 |
| Other Study ID Numbers: |
114461 |
| First Posted: | April 11, 2011 Key Record Dates |
| Results First Posted: | February 29, 2012 |
| Last Update Posted: | June 19, 2017 |
| Last Verified: | May 2017 |
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5-alpha-reductase inhibitor prostate surgery alpha-blocker |
enlarged prostate acute urinary retention Benign prostatic hyperplasia |
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Prostatic Hyperplasia Hyperplasia Pathologic Processes Prostatic Diseases |

