NCT00064649TerminatedPhase 3
Minimally Invasive Surgical Therapy Consortium for Benign Prostatic Hyperplasia
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)7 sites in 1 country49 target enrollmentStarted: April 2004Last updated:
Conditions
Interventions
Drugs
Trial Snapshot
- Phase
- Phase 3
- Status
- Terminated
- Enrollment
- 49
- Locations
- 7
Study Overview
Brief Summary
The primary objective of this randomized clinical trial is to determine the efficacy and safety of three treatments for benign prostatic hyperplasia (BPH): transurethral needle ablation (TUNA), transurethral microwave therapy (TUMT), and medical therapy with alfuzosin and finasteride.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 50 Years to — (Adult, Older Adult)
- Sex
- Male
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
2
Active Comparator
Transurethral Needle Ablation (TUNA)
Intervention: Transurethral Needle Ablation (TUNA) Therapy (Device)
3
Active Comparator
finasteride in a daily dose of 5 mg and alfuzosin in a daily dose of 10 mg
Intervention: Finasteride and Alfuzosin (Drug)
1
Active Comparator
Transurethral Microwave Thermotherapy (TUMT)
Intervention: Transurethral Microwave Thermotherapy (TUMT) (Device)
Investigators
Study Sites (7)
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