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NCT07305298Not yet recruiting

Mirabegron in Patients With Age-Related Macular Degeneration

Mirabegron in Patients With Age-Related Macular Degeneration Treated for Overactive Bladder: A Study Protocol for a Non-Randomized Prospective Controlled Trial

Source: ClinicalTrials.gov · Last updated 6 Feb 2026

Brief summary (registry, in English)

The goal of this clinical trial is to learn if Mirabegron works to treat dry AMD in patients, aged between 50 and 80 years-old, with early or moderate dry AMD and overactive bladder. The main question it aims to answer is: • Is there any change in outer retina morphology in patients treated? Researchers will compare the safety and efficacy of mirabegron versus conventional approach (Solifenacin) to treat dry AMD in patients with dry AMD and overactive bladder. Participants will: * Take Mirabegron or Solifenacin every day for 12 months * Visit the clinic once every 6 months for checkups and tests

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
312 (estimated)
First submitted
27 Nov 2025
Start date
1 Apr 2026
Primary completion date
1 Dec 2026
Lead sponsor
University of Naples
NCT number
NCT07305298

What you commit to

  • Study type: Observational
  • Planned participants: 312
  • From 1 Apr 2026 to the primary completion date, 1 Dec 2026
  • 1 site 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.

Lab values

  • • Any medical condition which contraindicates the use of beta-agonists
    • Uncontrolled hypertension
    • Tachycardia or atrial fibrillation
    • Any allergies to the beta-agonists
    • Renal or hepatic failure
    • Long QT or concomitant treatment with drugs that cause lengthening of the QT interval
    • Any sign of ocular inflammation
    • xudative AMD
    • Any ongoing medical or surgical treatment for AMD (including intravitreal injections, oral supplementation of lutein, zeaxanthin and or high dietary intake of antioxidants)
    • Any other ophthalmic diseases such glaucoma, acute or chronic uveitis, advanced cataract, or any opacities of the ocular media that do not permit high-quality imaging examinations.
    • Pregnancy
    • Any condition or disease that in the opinion of the investigators may put the subject at significant risk or may interfere significantly with the subject's participation in the study (i. e. malignancy, uncontrolled or cardiovascular diseases)

Who the study is looking for

  • Age subjects 50 and 80 years-old
  • Ability to express informed consent
  • Early or moderate dry AMD according to ARDS classification
  • Overreactive bladder
  • Visual acuity greater than BCVA 65 EDTRS letters.

Age in the registry: 50 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Federico II
Coordinator of this site? Confirm its status
NaplesItalyUnknown status

Related publications

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