Clinical Trial

Zinc Supplementation With Botulinum Toxin for Overactive Bladder

Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
This randomized, double-blind, placebo-controlled trial evaluates whether oral zinc plus phytase supplementation modifies clinical response to intradetrusor botulinum toxin injection in patients with overactive bladder. Participants will receive either zinc plus phytase supplementation or matching placebo for five days prior to intradetrusor botulinum toxin injection. Participants will be followed for six months after treatment to assess need for repeat botulinum toxin injection, urinary symptoms, and patient-reported outcomes related to overactive bladder.
Protocol Amendment History 1 change
notable Primary completion pushed: 2026-05 -> 2026-12 2026-07-03
Trial Details
NCT Number NCT07405554
Lead Sponsor Endeavor Health
Conditions Overactive Bladder (OAB)
Enrollment 72 participants
Start Date 2026-02-26
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-07-02