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NCT07187466Not yet recruitingPhase 4

Behavioral and/or Mirabegron to Treat Urinary Symptoms in Parkinson Disease

Sequential Multiple Assignment Randomized Trial to Treat Urinary Symptoms in Parkinson Disease

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to learn about different treatments for overactive bladder symptoms in Parkinson's Disease. The investigators want to find out if people who do not respond to one treatment (either behavioral or drug treatment) will respond to combined treatment. The investigators also want to find out what factors influence whether someone responds to the treatments.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
146 (estimated)
First submitted
18 Sept 2025
Start date
9 Nov 2026
Primary completion date
31 Mar 2030
Lead sponsor
VA Office of Research and Development
NCT number
NCT07187466

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 146
  • From 9 Nov 2026 to the primary completion date, 31 Mar 2030
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous intensive pelvic floor muscle exercise training
  • Previous artificial urinary sphincter, sling procedure or implanted sacral neuromodulation device
  • Current use of a bladder relaxant - permitted to enroll after one-week washout

Other illness

  • Significant cognitive impairment, as indicated by a Montreal Cognitive Assessment (MoCA) score of \< 18 or a telephone-MoCA score \< 13, which is the recommended diagnostic cut point for dementia in Parkinson's Disease (PD).
  • Chronic renal failure and on hemodialysis
  • Genitourinary cancer with ongoing surgical or external beam radiation treatment
  • History of bladder-injection of botulinum toxin in the last 12 months
  • Any unstable health condition expected to result in hospitalization or death within in the next 3 months as determined by principal investigator.
  • Hypersensitivity to drug class
  • Contraindication to the study drug (mirabegron) including history of acute urinary retention requiring catheterization

Lab values

  • Poorly controlled diabetes defined by a hemoglobin A1c (HgbA1c) of \>9.0% within the last 3 months. Participants with poorly controlled diabetes will be offered enrollment if the overactive bladder (OAB) symptoms persist after improvement in diabetes control
  • Hematuria on microscopic examination in the absence of infection. A urologic consultation will be recommended, and enrollment will depend on clearance by a urologist and agreement by the site PI that entry into the treatment protocol is not contraindicated

Other

  • Clinically significant depression as measured by a Geriatric Depression Scale-Short Form score of 10 or higher which could affect motivation to fully engage in the intervention
  • Use of an indwelling urinary catheter
  • Post-void residual urine measurement by bladder ultrasound of \> 150 milliliters (mL)
  • Severe uterine prolapse past the vaginal introitus
  • If on diuretic, dose should be stable for at least 4 weeks
  • If taking an alpha-blocker, dose should be stable for at least 4 weeks
  • If taking dutasteride or finasteride, dose should be stable for at least 6 months

Who the study is looking for

  • Clinical diagnosis of Parkinson's Disease (PD) determined by a board-certified neurologist with specialty training in movement disorders
  • An ICIQ-OAB Symptom Score of 7 or higher, which indicates clinically significant symptoms of OAB, defined as presence of urinary urgency with or without urgency incontinence usually with increased daytime frequency and nocturia in the absence of infection or other obvious pathology

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Atlanta VA Medical and Rehab Center, Decatur, GA
Coordinator of this site? Confirm its status
DecaturUnited StatesUnknown status
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
VA Salt Lake City Health Care System, Salt Lake City, UT
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.