Investigating the Adjunctive Use of Mirabegron in the Early Post-Rezum Procedure Period

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexMale
Age50+
SponsorUniversity of Manitoba

About this trial

The investigators propose conducting a randomized controlled trial at the Men's Health Clinic to evaluate whether patients who start and continue mirabegron postoperatively after undergoing Rezum therapy experience enhanced patient-reported outcomes, improved quality of life (QoL), and comparable rates of adverse events. There are no predicted adverse events of this study. There are no identified potential harms of this study.

Eligibility criteria

Qualifiers

age >50, symptomatic LUTS with IPSS ≥ 10

prostate volume 30-80cc on any imaging modality

Qmax between 5 and 15ml/s with minimum voided volume of 125cc

frequency ≥ 8 voids/day.

Disqualifiers

PVR greater than 300ml

active UTI within past week

previous surgical intervention for BPH

documented urethral stricture disease

Trial design

Treatments tested in this trial

  • Beta-3 agonists (Mirabegron/Myrbetriq)
  • Placebo group post rezum

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators