Evaluation of Repeating Low-intensity Shockwave Therapy (LiST) for Refractory Non-bacterial Prostatitis/Pelvic Pain Syndrome: a Single Arm Prospective Study
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 50
- Primary Endpoint
- The change of the pain domain of NIH-CPSI score from baseline to 12 weeks after final treatment.
Study Overview
Brief Summary
The aim of the study is to investigate the efficacy and safety of LiST retreatment for CP/CPPS patients.A total of 50 patients with CP/CPPS diagnosis who were previously treated with 6 sessions of LiST will participate in this study.The primary study parameter is the CP/CPPS-related pain complaints and it will be assessed by the NIH-CPSI
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 60 Years (Adult)
- Sex
- Male
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Participant must be between 18-60 years of age.
- •Participant has signed and dated the appropriate Informed Consent document.
- •Participant has had a clinical diagnosis of CP/CPPS defined as symptoms of discomfort or pain in the perineal or pelvic region for at least a three (3) month period within the last six (6) months.
- •Participant has received 6 sessions (1/week or 2/week, energy level 7, Dornier ARIES 2) of LIST the last 12 months for the treatment of CP/CPPS reporting amelioration but without complete remission of CP/CPPS symptoms ( at over 1 UPOINT positive domain).
Exclusion Criteria
- •Participant has evidence of facultative Gram negative or enterococcus with a value of ≥ 1000 CFU/ml in mid-stream urine (VB2).
- •Participant has a history of prostate, bladder or urethral cancer.
- •Participant has undergone pelvic radiation or systemic chemotherapy.
- •Participant has undergone intravesical chemotherapy.
- •Participant has unilateral orchialgia without pelvic symptoms, active urethral stricture or bladder stones, or any other urological condition associated with LUTS, any neurological disease or disorder affecting the bladder.
- •Participant has undergone prostate surgery or treatment.
- •Participant with penile or urinary sphincter implants.
- •Participant has been diagnosed with cancer during the last 5 years, or had any surgery in the pelvis.
- •Participant has a neurological impairment or psychiatric disorder preventing his understanding of consent and his ability to comply with the protocol.
Arms & Interventions
Group
LiST active treatment group
Intervention: Dornier Aries 2 device (Device)
Outcomes
Primary Outcomes
The change of the pain domain of NIH-CPSI score from baseline to 12 weeks after final treatment.
Time Frame: from baseline to 12 weeks after final treatment.
CP/CPPS-related complaints will be assessed by the the National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI). The questionnaire designed to provide symptom scores for patients with chronic prostatitis. The index provides scores on pain (items 1-4), urinary symptoms (items 5-6), and quality of life (items 7-9).Total score ranges from 0 to 35 (higher values represent worse outcome).The index provides a special pain domain (items 1-4) and the score for this domain ranges from 0 to 21.
Secondary Outcomes
- The difference between the LiST and sham group in the change of UPPOINTS phenotype- number of positive domainsfrom baseline to 4 and 12 weeks after final(baseline, 4 and 12 weeks after final treatment)
- The change of IIEF-ED score from baseline to 4 and 12 weeks after final treatment(baseline, 4 and 12 weeks after final treatment)
- The change of the pain domain of NIH-CPSI score from baseline to 4 weeks after final treatment.(from baseline to 4 weeks after final treatment.)
- The change of total NIH-CPSI score (Q1-9)from baseline to 4 and 12 weeks after final treatment(baseline, 4 and 12 weeks after final treatment)
- The change of quality of life domains (Q 7-9) of the NIH-CPSI score from baseline to 4 and 12 weeks after final treatment(baseline, 4 and 12 weeks after final treatment)
- The change of urinary symptoms (Q 5-6) and quality of life domains (Q 7-9) of the NIH-CPSI score from baseline to 4 and 12 weeks after final treatment(baseline, 4 and 12 weeks after final treatment)
Investigators
Dimitrios Hatzichristou
Professor
Institute for the Study of Urological Diseases, Greece