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Study identifier: NCT07405554 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Zinc Supplementation With Botulinum Toxin for Overactive Bladder

Condition: Overactive Bladder (OAB)  ·  Sponsor: Endeavor Health

PhasePhase 2
Planned participants72
Who can joinFemale, 21 Years to 100 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Ana Burgos, MD  ·  847-570-4729  ·  ana.burgos@endeavorhealth.org

Jungeun Lee  ·  847-570-4729  ·  jungeun.lee@endeavorhealth.org

Always discuss trial participation with your own doctor first.

Locations (1)

Endeavor HealthSkokie, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07405554