Dutasteride for Improving Peri-Operative and Long-Term Outcomes of Photoselective Vaporization of the Prostate (DOP)

NCT00274417 | Unknown

• 1 other identifier: UVA-001
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 2

Brief Summary

This study is for individuals electing to have GreenLight Photoselective Vaporization of the Prostate (PVP) to treat symptoms from an enlarged prostate gland. The purpose of this research study is to evaluate the safety and effectiveness of the medication dutasteride as compared to placebo (an inactive substance) for improving surgical and long-term outcomes of PVP. Dutasteride is approved by the United States Food and Drug Administration (FDA) for the treatment of symptoms from an enlarged prostate gland. The use of dutasteride to improve the outcomes of PVP is investigational. The study will last for approximately 15 months and will involve 6 visits.

Conditions

Benign Prostatic Hyperplasia; Lower Urinary Tract Symptoms

Outcome Measures

Primary Outcomes (1)

• Change in American Urologic Association Sympton Score

Secondary Outcomes (7)

• Change in BPH Quality of Life

• Change in urinary flow rate

• Change in post void residual

• PVP operation time, wattage use, estimated blood loss

• Post-operative catheter time

Interventions

dutasteride DRUG

Eligibility Criteria

• Age: 50 Years+
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• \. Men aged ≥ 50 years old 2. Subjects with LUTS due to BPH with:
• AUA SI score ≥ 12 at baseline
• Qmax ≤ 15 mL/sec (on at least 125 mL)
• Symptoms for ≥ 3 months 3. Subjects with prostate volume ≥ 30 grams 4. Subjects who are appropriate surgical candidates for Photoselective Vaporization of the Prostate (PVP) as determined by a study investigator 5. Subjects able to swallow and retain oral medication 6. Subjects able to comply with study protocol 7. Subjects able to read and write (to complete the self-administered AUA SI) 8. Subjects who sign the approved Informed Consent Form for the study

You may not qualify if:

• Subjects who have previously undergone a surgical treatment for BPH including but not limited to TURP, TUNA, TUIP, thermotherapy, prostatic stent, dilation balloon, etc.
• Subjects with a history of prostate cancer
• Subjects with a history of bladder or testicular cancer in the past 5 years
•  Subjects who have been cancer-free for at least 5 years will be eligible
•  Subjects with a history of superficial bladder cancer will not be excluded
• Subjects who have received radiation to the pelvis or prostate or radical surgery to the pelvic area
• Subjects with persistent gross hematuria, current symptomatic prostatitis
• Subjects with neurogenic bladder and/or sphincter abnormalities for any reason including Parkinson's disease, multiple sclerosis, stroke, or diabetes
• Subjects who have used any 5 α-reductase inhibitors in the past 3 months.
•  Subjects who wash-out of these medications for 3 months prior to screening will be eligible
• Subjects taking alpha-blockers within 2 weeks prior to randomization.
•  Subjects must be off of alpha blockers at the time of randomization for the measurement of AUA Symptom Score, QoL Score, flow rate, post void residual, etc. In the rare case a patient goes into retention during the 3 month period between randomization and PVP, they will be allowed to resume their alpha blocker until the PVP since no outcomes are measured during this period. They will be required to discontinue the alpha blocker after they have surgery
• Subjects on an unstable regimen of antidepressants, anticholinergics, androgens, or herbal supplements including phyto-sterols (such as saw palmetto)  Subjects who are on a stable regimen of the above medications for at least 1 month prior to screening and are willing to stay on the same dose for the duration of the study will be eligible
• Subjects on an unstable regimen of beta-blockers, antihistamines, anticonvulsants, antispasmodics, or other medications known to affect the clinical symptoms of BPH
•  Subjects who are on a stable regimen of the above medications for at least 4 months prior to screening and are willing to stay on the same dose for the duration of the study will be eligible

Sponsors & Collaborators

• Urology of Virginia: lead
• GlaxoSmithKline: collaborator

Study Sites (2)

Urology of Virginia

Norfolk, Virginia, 23510, United States

Location

Urology of Virginia

Virginia Beach, Virginia, 23454, United States

Location

MeSH Terms

Conditions

Prostatic Hyperplasia; Lower Urinary Tract Symptoms

Interventions

Dutasteride

Condition Hierarchy (Ancestors)

Prostatic Diseases; Genital Diseases, Male; Genital Diseases; Urogenital Diseases; Male Urogenital Diseases; Urological Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Azasteroids; Steroids, Heterocyclic; Steroids; Fused-Ring Compounds; Polycyclic Compounds

Study Officials

• Gregg Eure, MD

  Urology of Virginia Research, Devine-Tidewater Urology

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: January 9, 2006
• First Posted: January 10, 2006
• Study Start: January 1, 2006
• Study Completion: May 1, 2009
• Last Updated: April 18, 2007

Record last verified: 2007-04

Locations

US (2)