NCT07214675 The Edison System for Treatment of Benign Prostatic Hyperplasia (BPH) Using Histotripsy
| NCT ID | NCT07214675 |
| Status | Recruiting |
| Phase | — |
| Sponsor | HistoSonics, Inc. |
| Condition | Benign Prostatic Hyperplasia |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2026-03-20 |
| Primary Completion | 2027-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 80 participants in total. It began in 2026-03-20 with a primary completion date of 2027-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The purpose of this trial is to evaluate the safety of histotripsy using the HistoSonics Edison System for treatment of BPH.
Eligibility Criteria
Inclusion Criteria: 1. Subject is ≥ 50 years of age. 2. Subject has signed the Ethics Committee (EC) approved trial Informed Consent Form (ICF) prior to any trial related tests/procedures and is willing to comply with trial procedures and required follow-up assessments. 3. Subject is diagnosed with BPH. 4. Subject has a Body Mass Index (BMI) \< 27. 5. Subject has an I-PSS ≥ 15. 6. Subject has a prostate volume \> 30 mL and ≤ 150 mL. 7. Subject has a Qmax ≤ 15 mL/s with a voided volume of ≥ 125 mL during a uroflow test. 8. Subject accepts the potential loss of ejaculatory function. 9. Subject can tolerate general anesthesia. Index-Procedure Imaging Inclusion (Assessed day of procedure) 10. Subject has an adequate acoustic window to visualize the prostate using the HistoSonics Edison System. 11. Target treatment volume is ≥ 1 cm from the rectum as visualized on ultrasound, CT or MR imaging. Exclusion Criteria: 1. Subject has a life expectancy of less than one (1) year. 2. Subject has a known sensitivity to contrast media and cannot be adequately pre-medicated. 3. Subject has a post-void residual ≥ 150 mL confirmed via ultrasound. 4. Subject has an estimated glomerular filtration rate (eGFR) ≤ 50 mL/min, ≤ 14 days prior to the planned index procedure date. 5. Subject has uncorrectable coagulopathy. 6. Subject has an International Normalized Ratio (INR) value ˃ 2.0, ≤14 days prior to the planned index procedure date. 7. Subject has had a prostatectomy. 8. Subject has acute prostatitis. 9. Subject has a diagnosis of or has received treatment for chronic prostatitis or chronic pelvic pain syndrome. 10. Subject has had a urinary tract infection (UTI) ≤ 3 months prior to the planned index procedure date. 11. Subject has bladder stones. 12. Subject is catheter dependent or has a history of intermittent self-catheterization. 13. Presence of prostatic calcifications in the planned treatment volume (PTV). 14. Presence of permanent radioactive implants in the rectal wall. 15. Subject has has a major abdominal or rectal surgery that inhibits visualization of the prostate. 16. Subject has undergone prior locoregional therapy (e.g., Rezum, laser, Urolift, TURP emboli, or radiation). 17. Subject has planned locoregional therapy 6 months post index procedure (e.g., Rezum, laser, Urolift, TURP emboli, or radiation). 18. Subjects who have active cancers (not in remission for the last two years) other than non-melanomatous skin cancers. 19. Subject is being actively treated in another pharmaceutical or device trial that has not completed its primary endpoint prior to the index procedure or may interfere with the primary outcome measure of this trial. 20. In the investigator's opinion, histotripsy is not a treatment option for the subject. 21. Subject has a concurrent condition that could jeopardize the safety of the subject or compliance with the protocol. 22. Subject's prostate is not treatable by the System's working ranges (refer to User Guide).
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07214675 clinical trial?
This trial is open to male participants only, aged 50 Years or older, studying Benign Prostatic Hyperplasia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07214675 currently recruiting?
Yes, NCT07214675 is actively recruiting participants. Contact the research team at Kelly.Erickson@histosonics.com for enrollment information.
Where is the NCT07214675 trial being conducted?
This trial is being conducted at Shatin, Hong Kong.
Who is sponsoring the NCT07214675 clinical trial?
NCT07214675 is sponsored by HistoSonics, Inc.. The trial plans to enroll 80 participants.