Clinical trial Recruiting at 1 site Phase 3 Interventional Ages 18 to 89 Men only

Using loop diuretics to improve same-day discharge after prostate surgery

Official title: Loop Diuretics During Morcellation to Improve Same-day Discharge Rates After Holmium Laser Enucleation of the Prostate (HoLEP)

Run by Northwestern University · NCT05620784 · Data updated 2026-11-12

This study is testing if giving a diuretic during prostate surgery can help men go home the same day by improving their recovery and reducing complications.

Quick facts

PhasePhase 3
Study typeInterventional
Ages18 Years to 89 Years
SexMen only
Enrollment138 (estimated)
SponsorNorthwestern University
Academic / other
Locations1 site (Chicago, Illinois)
StatusRecruiting
StartedMarch 1, 2023
Main results expectedJune 6, 2023
Study endsAugust 1, 2024
Registry record updatedSeptember 13, 2023
Trial IDNCT05620784 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are males aged 18 to 89 who are scheduled to undergo HoLEP for BPH.

Probably not a fit

Patients with allergies to furosemide, anuria, liver failure, or those undergoing concurrent surgeries may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the impact of intra-operative administration of furosemide on same-day discharge rates following Holmium Laser Enucleation of the Prostate (HoLEP) for benign prostatic hypertrophy (BPH). Patients will be randomly assigned to receive either 20mg of IV furosemide or a control treatment during the procedure. The study aims to determine if the use of furosemide significantly affects post-operative urinary output and reduces complications such as hematuria, thereby facilitating same-day discharge. The trial is conducted at Northwestern University and involves male patients aged 18 to 89 undergoing HoLEP.

Why it matters

Potential benefit: If successful, this study could enhance recovery protocols, allowing more patients to safely return home on the same day after surgery.

How similar studies have gone: While the use of furosemide in this context is common, this study is novel in its systematic evaluation of its effectiveness for same-day discharge rates.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Males 18 -89 undergoing HoLEP
* Willing to sign the Informed Consent Form
* Able to read, understand, and complete patient questionnaires.

Exclusion Criteria:

* Allergy or hypersensitivity to furosemide or other loop diuretic
* Anuric patients or patients with liver failure
* Patients having a concurrent ureteroscopy +/- laser lithotripsy, percutaneous nephrolithotomy, or non-urologic surgery at the time of their HoLEP
* Anticipated need for perineal urethrostomy at the time of HoLEP
* Patient not undergoing catheter removal and voiding trial at Northwestern Memorial Hospital

Where it's running

  • Northwestern University
    Chicago, Illinois, United States
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.