Rezum FIM Optimization Study

Not Applicable

Completed

• Conditions: Adenoma, Prostatic; Prostatic Adenoma; Rezum; Benign Prostatic Hyperplasia; Prostatic Hypertrophy, Benign; Prostatic Hyperplasia, Benign; Prostatic Hypertrophy
• Interventions: Device: Rezum System

• Registration Number: NCT02940392
• Lead Sponsor: Boston Scientific Corporation

Brief Summary

Evaluate the effect of the NxThera BPH Rezum System on prostate tissue in subjects suffering from LUTS symptoms secondary to benign prostatic hyperplasia (BPH).

Detailed Description

Subjects with BPH symptoms were treated with the Rezum device with a range of thermal energies (as measured by calorie output) to optimize the setting for maximum lesion size with minimal intra and post-procedure discomfort. Lesion size and ablated tissue resorption rate was followed post-procedure at 1 week, 1 month, 3 months, and 6 months.

Study Timeline

• Study Start: 2012-03-19
• Study First Submitted: 2016-10-19
• Study First Submitted QC: 2016-10-19
• Study First Posted: 2016-10-20
• Primary Completion: 2017-05-19
• Study Completion: 2017-05-19
• Results First Submitted: 2020-12-18
• Status Verified: 2021-02
• Results First Submitted QC: 2021-02-12
• Last Update Submitted: 2021-02-12
• Results First Posted: 2021-03-05
• Last Update Posted: 2021-03-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 15

Inclusion Criteria

1. Male subjects > 45 years of age who have symptomatic / obstructive symptoms secondary to BPH requiring invasive intervention.
2. IPSS score of ≥ 15.
3. Qmax: Peak flow rate ≤ 15 ml/sec.
4. Post-void residual (PVR) < 300 ml.
5. Prostate transverse diameter > 30 mm.
6. Prostate volume between 20 to 120 gm.
7. Voided volume ≥ 125 ml.
8. Subject able to complete the study protocol in the opinion of the Principal Investigator.
9. Subject must be willing to undergo the procedure without anesthesia.

Exclusion Criteria

1. History of any illness or surgery that in the opinion of the Principal Investigator may confound the results of the study.

2. Presence of a penile implant.

3. Any prior minimally invasive intervention (e.g. TUNA,Laser, Microwave) or surgical intervention for the symptoms of BPH.

4. Currently enrolled in another clinical trial.

5. Confirmed or suspected malignancy of prostate or bladder.

6. Previous rectal surgery (other than hemorrhoidectomy) or history of rectal disease.

7. Previous pelvic irradiation or radical pelvic surgery.

8. Documented active urinary tract infection by culture or bacterial prostatitis within last year documented by culture (UTI is defined as >100,000 colonies per ml urine from midstream clean catch or catheterization specimen).

9. Neurogenic bladder or sphincter abnormalities.

10. Urethral strictures, bladder neck contracture or muscle spasms.

11. Bleeding disorder (note that use of anti-platelet medication is not an exclusion criterion).

12. Subjects who are interested in maintaining fertility.

13. Use of concomitant (or recent) medications to include the following:

    1. Beta blockers, antihistamines, anticonvulsants, and antispasmodics within 1 week of treatment, unless there is documented evidence of stable dosing for last 6 months (e.g., no dose changes).
    2. Alpha blockers, antidepressants, anticholinergics, androgens, or gonadotropin-releasing hormonal analogs within 2 weeks of treatment.
    3. 5-alpha reductase inhibitor within the last 6 months

14. Subject is unable or unwilling to go through a "washout" period for the above medications prior to treatment.

15. Subject has chronic urinary retention.

16. Significant urge incontinence.

17. Poor detrusor muscle function.

18. Neurological disorders which might affect bladder or sphincter function.

19. Bladder stones.

20. Renal impairment.

21. In the opinion of the Principal Investigator, subject will not be able to adequately tolerate a rigid cystoscopy-type procedure.

22. Unable or unwilling to sign the Informed Consent Form (ICF) and/or comply with all the required follow-up requirements.

23. Any cognitive disorder that interferes with or precludes a subject from directly and accurately communicating with the Principal Investigator regarding the study.

24. Peripheral arterial disease with intermittent claudication or Leriches Syndrome (i.e., claudication of the buttocks or perineum).

25. Biopsy of the prostate within 30 days prior to the Rezūm procedure.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Rezum Treatment	Rezum System	Patients will receive the Rezūm transurethral needle ablation procedure to treat benign prostatic hyperplasia.

Primary Outcome Measures

Name	Time	Method
Change in International Prostate Symptom Score	Baseline to 1 week, 1 month, 3 months, 6 months, 1 year, annually to 5 years	International Prostate Symptom Score (IPSS) scores were recorded at Baseline to 1 week, 1 month, 3 months, 6 months, 1 year, then annually to 5 years. The mean change in IPSS was calculated.; The IPSS is a validated questionnaire used to screen for, rapidly diagnose, track the symptoms of, and suggest management of the symptoms of benign prostatic hyperplasia (BPH). Scoring ranges from 0 to 35 with overall scores of 0-7 correlated to mildly symptomatic, 8-19 correlated to moderately symptomatic and 20-35 correlated to severely symptomatic. A reduction in score from baseline corresponds to improved outcome post procedure.

Trial Locations

Locations (1)

Clinica Canela; 🇩🇴 La Romana, Dominican Republic