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A Post Marketing Surveillance Study Of Doxazosin Mesylate GITS Among Filipino Patients With Benign Prostatic Hyperplasia (BPH)

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Viatris

Status

Completed

Conditions

Prostatic Hyperplasia

Treatments

Drug: Doxazosin mesylate GITS

Study type

Observational

Funder types

Industry

Identifiers

NCT01003886
A0351068

Details and patient eligibility

About

This study aims to assess the safety, tolerability and efficacy of Doxazosin GITS in Filipino patients diagnosed with Benign Prostatic Hyperplasia (BPH) under the usual clinical care setting.

Full description

This is an open label study. All patients prescribed with Doxazosin GITS can be enrolled in this study.

Enrollment

989 patients

Sex

Male

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects that will be included must be consistent with the approved label indication of Doxazosin mesylate GITS in the Philippines, which includes adult male diagnosed with BPH, and who are prescribed with Doxazosin mesylate GITS.

Exclusion criteria

  • Subjects with condition that are contraindicated with Doxazosin mesylate GITS based on the approved labeling in the Philippines.

Trial design

989 participants in 1 patient group

Open Label
Description:
Adult male diagnosed with BPH and prescribed with Doxazosin mesylate GITS
Treatment:
Drug: Doxazosin mesylate GITS

Trial contacts and locations

73

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Data sourced from clinicaltrials.gov

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