🔎 Trials Near Me

Home › Enlarged Prostate (BPH) › NCT07377929

Intradetrusor Onabotulinumtoxin A (Botox) at the Time of Transurethral Resection of the Prostate or Transurethral Waterjet Ablation of the Prostate for Mixed Lower Urinary Tract Symptoms

RecruitingObservational study

Who can join

Ages 18 and older · Men

Full eligibility criteria
Inclusion Criteria:

1. Male \>= 18 years of age and being scheduled to undergo TURP or Aquablation and Botox procedure.
2. Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.

   Exclusion Criteria:
3. Non-English speaking
4. Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
5. History of receiving Botox in the bladder, within the previous 12 months.

About the study

Patients with longstanding obstructive lower urinary tract symptoms (LUTS) due to benign prostatic hypertrophy (BPH) can also develop symptoms of overactive bladder syndrome (OAB). Transurethral resection of the prostate (TURP) and Transurethral Waterjet Ablation of the Prostate (Aquablation) are amongst the gold standard surgical treatments for BPH. However, in the immediate post-operative period, TURP and Aquablation can also include OAB-like symptoms, including urinary frequency and urgency. For men with baseline OAB symptoms, this initial worsening of symptoms can be distressing.

Botox is an FDA approved medication with on-label indications to treat overactive bladder.

The purpose of this study is to evaluate the outcomes of men who have Botox concurrent with their TURP or Aquablation.

What is being tested

Sponsor: Benaroya Research Institute · Participants: 20 · Started: Jan 19, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07377929

Locations in the U.S.

WashingtonVirginia Mason Franciscan Health, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.