- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01876706
UroLift System TOlerability and ReCovery When Administering Local Anesthesia (LOCAL)
L.O.C.A.L. Study -- UroLift System TOlerability and ReCovery When Administering Local Anesthesia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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San Diego, California, United States, 92123
- Genesis Research LLC
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Florida
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Daytona Beach, Florida, United States, 32114
- Advanced Urology Institute
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Saint Petersburg, Florida, United States, 33710
- Pinellas Urology
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Maryland
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Baltimore, Maryland, United States, 21237
- Chesapeake Urology
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Nevada
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Las Vegas, Nevada, United States, 89144
- Sheldon J. Freedman, M.D., Ltd.
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South Carolina
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Myrtle Beach, South Carolina, United States, 29572
- Carolina Urologic Research Center
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Utah
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Salt Lake City, Utah, United States, 84124
- Jean Brown Research
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Males age of 50 years or older diagnosed with symptomatic benign prostatic hyperplasia (BPH)
Exclusion Criteria:
- Size, volume,length of prostate
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: UroLift® System
Single-arm of qualified subjects receiving UroLift® System intervention.
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The NeoTract UroLift System is a medical device approved for sale in the European Union, Australia, and Canada.
The UroLift® System is indicated for the treatment of symptoms due to urinary outflow obstruction secondary to benign prostatic hyperplasia (BPH) in men 50 years of age or older.
During the procedure, an implant is delivered into the prostatic lobe obstructing the urethra and restricting urine flow.
The distal end of the device is used to compress the lobe then the implant is delivered to retain the lobe in position, thereby increasing the urethral opening and reducing the fluid obstruction through the prostatic urethra.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Quality of Recovery
Time Frame: 1 Month
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Primary effectiveness will be achieved when 80% (95% lower confidence limit) of subjects achieve a score of 80 or more on the Quality of Recovery Visual Analog Scale (QoR VAS) by the one month follow-up visit.
The VAS scale is 0-100, with 100 being 100% recovery.
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1 Month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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IPSS Scores at Baseline and 12 Month Follow-up
Time Frame: 12 Months
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The International Prostate Symptom Score (IPSS) is an 7 question written screening tool used to screen for, rapidly diagnose, track the symptoms of, and suggest management of the symptoms of the disease benign prostatic hyperplasia (BPH). Lower scores are indicative of less symptoms. Score Correlation[1] 0-7 Mildly symptomatic 8-19 Moderately symptomatic 20-35 Severely symptomatic |
12 Months
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IPSS 12 Month Change From Baseline
Time Frame: 12 Months
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The International Prostate Symptom Score (IPSS) is an 7 question written screening tool used to screen for, rapidly diagnose, track the symptoms of, and suggest management of the symptoms of the disease benign prostatic hyperplasia (BPH) using a total score from 0 - 35. The larger number for Change in IPSS Score 12 Month Follow-up from Baseline, demonstrate the improvement in IPSS. |
12 Months
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IPSS 12 Month Percent (%) Change From Baseline
Time Frame: 12 Months
|
The International Prostate Symptom Score (IPSS) is an 7 question written screening tool used to screen for, rapidly diagnose, track the symptoms of, and suggest management of the symptoms of the disease benign prostatic hyperplasia (BPH) using a total score from 0 - 35. The larger Percent (%) Change in IPSS Score at 12 Month Follow-up from Baseline, demonstrates the improvement in IPSS (the mean score was change by X %). Note: Percent (%) Change: is the mean % change of each subject. |
12 Months
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BPH II Scores at Baseline and 12 Month Follow-up
Time Frame: 12 Month
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BPH Impact Index (BPH II) A validated questionnaire to measure how much urinary problems of patients with benign prostatic hyperplasia affect domains of health. BPHII total score is the combined (sum) of scores for Questions 1-4 (sum range of 0-13 scoring is presented below) MAX of 13 would be 3,3,3,and 4: A score of zero = Patient experiences no BPH impact and does not add any to score. Questions 1-4:
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12 Month
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BPH II 12 Month Percent (%) Change From Baseline
Time Frame: 12 Months
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BPH Impact Index (BPH II) A validated questionnaire to measure how much urinary problems of patients with benign prostatic hyperplasia affect domains of health. BPHII total score is the combined (sum) of scores for Questions 1-4 (sum range of 0-13 scoring is presented below) MAX of 13 would be 3,3,3,and 4: A score of zero = Patient experiences no BPH impact and does not add any to score. Questions 1-4:
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12 Months
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BPH II 12 Month Change From Baseline
Time Frame: 12 Months
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BPH Impact Index (BPH II) A validated questionnaire to measure how much urinary problems of patients with benign prostatic hyperplasia affect domains of health. BPHII total score is the combined (sum) of scores for Questions 1-4 (sum range of 0-13 scoring is presented below) MAX of 13 would be 3,3,3,and 4: A score of zero = Patient experiences no BPH impact and does not add any to score. Questions 1-4:
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12 Months
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Qmax Scores at Baseline and 12 Month Follow-up
Time Frame: 12 Month
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QMAX indicates the maximum flow rate during a Uroflow in mL/sec.
QMAX is used as an indicator for the diagnosis of enlarged prostate.
A lower QMAX may indicate that the enlarged prostate puts pressure on the urethra.
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12 Month
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QMAX 12 Month Change Minus Baseline
Time Frame: 12 Months
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QMAX indicates the maximum flow rate during a Uroflow in mL/sec.
QMAX is used as an indicator for the diagnosis of enlarged prostate.
A lower QMAX may indicate that the enlarged prostate puts pressure on the urethra.
The larger number for Change of the QMAX value at 12 Month Follow-up minus Baseline, demonstrate the improvement in QMAX
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12 Months
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QMAX 12 Month Percent (%) Change in mL/Sec From Baseline
Time Frame: 12 Months
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QMAX indicates the maximum flow rate during a Uroflow in mL/sec.
QMAX is used as an indicator for the diagnosis of enlarged prostate.
A lower QMAX may indicate that the enlarged prostate puts pressure on the urethra.
The larger Percent (%) Change of the QMAX value at 12 Month Follow-up from Baseline, demonstrate the improvement in QMAX.
Note: Percent (%) Change: is the average %change of each subject
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12 Months
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Pain Tolerability Throughout the UroLift System Procedure
Time Frame: 12 Month
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Pain Tolerability using questionnaire pelvic pain Visual Analog Scale (VAS) 0-10.
A score of 0 (zero) would equal no pain while a score of 10 would equate to pain as bad as patient could imagine.
This scale was assessed at different times during procedure as specified in results section.
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12 Month
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BPHII Baseline and 12 Month Median Score, 95% CI
Time Frame: 12 Month
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BPH Impact Index (BPH II) A validated questionnaire to measure how much urinary problems of patients with benign prostatic hyperplasia affect domains of health. BPHII total score is the combined (sum) of scores for Questions 1-4 (sum range of 0-13 scoring is presented below) MAX of 13 would be 3,3,3,and 4: A score of zero = Patient experiences no BPH impact and does not add any to score. Questions 1-4:
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12 Month
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IPSS at Baseline and 12 Months, Median , 95% CI
Time Frame: 12 Month
|
The International Prostate Symptom Score (IPSS) is an 7 question written screening tool used to screen for, rapidly diagnose, track the symptoms of, and suggest management of the symptoms of the disease benign prostatic hyperplasia (BPH). Lower scores are indicative of less symptoms. Score Correlation[1] 0-7 Mildly symptomatic 8-19 Moderately symptomatic 20-35 Severely symptomatic |
12 Month
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QMAX Median at Baseline and 12 Months With CI 95%
Time Frame: 12 Month
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QMAX indicates the maximum flow rate during a Uroflow in mL/sec.
QMAX is used as an indicator for the diagnosis of enlarged prostate.
A lower QMAX may indicate that the enlarged prostate is obstructive.
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12 Month
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Neal D Shore, MD, Grand Strand Urology
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CP12911
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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