Last updated: 11/07/2018 07:01:50
Benefits of Adherence to 5-alpha reductase inhibitor treatment in Men with Enlarged Prostate: An Assessment of Medicare and Medicaid Patients Using the MarketScan Database
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Benefits of Adherence to 5-alpha reductase inhibitor treatment in Men with Enlarged Prostate: An Assessment of Medicare and Medicaid Patients Using the MarketScan Database
Trial description: Adherence and length of treatment with a 5-alpha reductase inhibitor (5ARI) therapy may be associated with improved clinical outcomes for patients with enlarged prostates (EP) and lower health care related costs. The objectives of this study are to quantify 1.) the relationship between 5ARI adherence and length of therapy and the likelihood of acute urinary retention (AUR), prostate-related surgery (emergency and non-emergency), and clinical progression (defined as AUR and/or prostate-related surgery); and 2.) the monthly EP-related, medical costs in a Medicaid and Medicare population. The null hypothesis is that no differences will be observed in the outcomes and costs of patients who adhere to long-term 5ARI therapy and those who do not. The test hypothesis is that patients with higher levels of adherence to 5ARI for a longer period of time will experience significantly fewer adverse outcomes and significantly lower treatment costs. The data source for this analysis is the MarketScan database, which contains medical and pharmacy claims for commercial health plan members and Medicare recipients. Medical and pharmacy claims data are sourced directly from health plans and employers. The database represents approximately 18 to 20 million individuals annually and nearly 22 million Medicaid enrollees from multiple states. The database includes the Medicare-covered portion of payment, the employer-paid portion, and any out-of-pocket expenses paid by the beneficiary.The study design is a retrospective cohort analysis. Each patient's index date was defined as the date of the first fill for a 5ARI prescription.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Mean number of patients with a diagnosis code for acute urinary retention (AUR) and/or a procedure code for prostate surgery
Timeframe: 1 year following the first therapy date or until an event that signifies clinical progression is observed (whichever occurs first)
Secondary outcomes:
Adjusted benign prostatic hyperplasia (BPH)-related costs
Timeframe: 1 year following the first therapy date
Medication Possession Ratio (MPR)
Timeframe: 1 year following the first therapy date
Interventions:
Enrollment:
28903
Primary completion date:
Not applicable
Observational study model:
Cohort
Time perspective:
Retrospective
Clinical publications:
Eaddy MT, Kruep EJ, Lunacsek O, Goodwin B. Establishing the Clinical and Economic Benefits of Adherence to 5-Alpha Reductase Inhibitors in Enlarged Prostate: An Assessment of Medicare and Medicaid Patients. Expert Opin Pharmacother. 2012;13(18):2593-2600.
- Male
- Age 65 or older
- A prostate cancer diagnosis
- A procedure cost for any prostate-related surgical procedure prior to the index date
Inclusion and exclusion criteria
Inclusion criteria:
- Male
- Age 65 or older
- A diagnostic claim of BPH (ICD-9-CM code 222.2x or 600.xx)
- A prescription claim for a 5ARI for at least 60 days during the observation period
- Continuous eligibility for 6 months prior to and at least 91 days after the index date
Exclusion criteria:
- A prostate cancer diagnosis
- A procedure cost for any prostate-related surgical procedure prior to the index date
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2010-14-12
Plain language summaries
Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.
Additional information about the trial
Not applicable
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