INTUPRO in the Treatment of Benign Prostatic Hyperplasia-Related Symptoms

The main goal of this study is to determine how well INTUPRO improves urinary symptoms in patients with benign prostatic hyperplasia (BPH). Effectiveness will be measured by changes in the International Prostate Symptom Score (IPSS), a standard questionnaire used to assess urinary symptoms.

Another goal of this study is to evaluate the safety of INTUPRO. This includes monitoring and recording all side effects, complications, or other medical problems that occur during the procedure and during the follow-up period after treatment.

This study is planned to last approximately one year; each patient will be followed for 3 months after treatment. Enrollment of 30 patients is expected.

Inclusion criteria

• • Male patient aged 45 years or older

• Prostate volume greater than 30 grams
• An International Prostate Symptom Score (IPSS) of 12 or higher
• Presence of obstructive urinary symptoms, such as difficulty starting urination, leakage of urine after voiding, or a feeling of incomplete bladder emptying.

This criterion may include patients who have previously been diagnosed with prostate cancer and completed treatment, but are experiencing urinary problems.

• Life expectancy of at least 3 months
• Ability to understand the study information and provide written informed consent
• Willingness and ability to comply with all study requirements, including procedures, clinical assessments, and follow-up visits

Exclusion criteria

• Urethral stricture

• Bladder stones
• Prostate volume 120 grams or greater
• Presence of a prostate median lobe
• History of bladder cancer or kidney cancer, and/or prior surgery related to these conditions
• Previous radiation therapy to the pelvic region
• Prior invasive surgical treatment for BPH symptoms
• The Principal Investigator believes the patient would not tolerate the procedure
• Presence of a cognitive impairment that, in the opinion of the Principal Investigator, would interfere with the patient's ability to provide reliable data or to safely complete the study
• Bleeding disorders
• Known allergy or intolerance to MRI contrast agents required for imaging used to evaluate treatment effectiveness after ionic fluid application
• Other significant concurrent medical conditions that, in the investigator's judgment, could prevent clinical benefit from the procedure or could place the patient or study objectives at risk (including, but not limited to, active infection, kidney dysfunction, or significant comorbidities)
• Significant medical or psychiatric illness
• Participation in another clinical study involving a device, drug, or procedure that has not been completed or that could affect the outcomes of this study
• Inability or unwillingness to undergo MRI examinations during the study period for any reason