A Study of Tadalafil in Men With Benign Prostatic Hyperplasia Symptoms Who Are Being Treated With Alpha Blockers

Eli Lilly and Company318 enrolled

Overview

The purpose of this study is to evaluate the safety and efficacy of tadalafil when given to men who are currently taking a medication called an alpha blocker for the treatment of benign prostatic hyperplasia (BPH) symptoms (such as urinary frequency, urgency, and a feeling that the bladder is not completely emptied after urination).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

318

Conditions

Benign Prostatic Hyperplasia

Interventions

TadalafilDRUG

5 mg taken by mouth once daily for 12 weeks

PlaceboDRUG

By mouth once daily for 12 weeks

Eligibility

Sex: MALEMin age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Stable on alpha blocker therapy for the treatment of BPH for at least 4 weeks prior to starting the study. * Have not taken the following treatments within the indicated duration and agree not to use at any time during the study: 1. All other Benign Prostatic Hyperplasia therapy (including herbal preparations) for at least 4 weeks prior to receiving study medication. 2. Overactive Bladder therapy (including antimuscarinics) for at least 4 weeks prior to receiving study medication. 3. Erectile Dysfunction therapy (including herbal preparations) for at least 4 weeks prior to receiving study medication. * If taking finasteride or dutasteride, must have been taking treatment for at least 6 months. Exclusion Criteria: * Currently receiving alpha-blocker therapy for the treatment of hypertension. * History of symptoms associated with orthostasis, including recurrent episodes of dizziness, lightheadedness, loss of consciousness, or syncope. * Treated with nitrates for any cardiac conditions. * Have had any of the following in the past 90 days: Heart attack, also known as a myocardial infarction (MI); Heart bypass surgery (called coronary artery bypass graft surgery); Had a procedure to open up blood vessels in the heart known as angioplasty or stent placement (percutaneous coronary intervention). * Have problems with kidneys, liver, or nervous system * Have uncontrolled diabetes * Have prostate cancer, are being treated for cancer or have clinical evidence of prostate cancer (PSA greater than 10 ng/ml at the start of study). * Have had a stroke or a significant injury to brain or spinal cord.

Locations (31)

Outcomes

Primary Outcomes

Number of Men With Treatment-emergent Dizziness

The primary safety measure is the proportion (reported in numbers) of subjects experiencing treatment-emergent dizziness to include the Medical Dictionary for Regulatory Activities (MedDRA) preferred terms of dizziness, dizziness postural, and procedural dizziness. Treatment-emergent dizziness is defined as any of the predefined terms of dizziness that is first reported or worsens in severity after baseline.

Time frame: Baseline through 12 Weeks

Secondary Outcomes

Number of Participants With Positive Orthostatic Vital Signs Test; Shift From Any Pre-Randomization to Any Post-Randomization Visit

A positive orthostatic test is defined as at least one of the following 4 criteria being met at any pre-randomization or post-randomization visit: (1) reduction in systolic blood pressure of \>= 20 mmHg from the supine to standing position;(2)reduction in diastolic blood pressure of \>=10 mmHg from the supine to standing position;(3)increase in heart rate of \>= 20 bpm from the supine to standing position; or (4)Unable to remain standing. A negative orthostatic test is defined as none of the above 4 criteria (1, 2, 3, or 4) being met at any pre-randomization or post-randomization visit.

Time frame: Baseline through 12 Weeks

International Prostate Symptom Score (IPSS) Change From Baseline

Change from baseline to endpoint in IPSS Score. The IPSS Total Score is obtained by combining the scores of the responses to 1 through 7 component questions. Each question is scored from 0-5 for an IPSS range of 0-35 points; higher numerical scores from the IPSS questionnaire represent greater severity of symptoms.

Time frame: Baseline, 12 Weeks

Postvoid Residual Volume (PVR) Change From Baseline

Change from baseline to endpoint in PVR volume. PVR is obtained by measuring with ultrasound the remaining urine in the bladder after urination.

Time frame: Baseline, 12 Weeks

Data from ClinicalTrials.gov

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