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Study identifier: NCT06956209 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Akyva First In Human

Condition: Underactive Bladder  ·  Sponsor: Iota Biosciences, Inc

PhaseNA
Planned participants15
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this study is to check if the study device, the Akyva System, is safe to use and to find out if it has any possible side effects. Researchers will see if the study device can help you urinate without the need for catheterization, which involves passing a catheter (small tube) into the bladder, and if there is improvement in the leftover urine amount in your bladder after urinating or trying to urinate.

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

Talk to the study team

Akyva Study Team  ·  +1 925-788-5929  ·  akyvastudy@iota.bio

Always discuss trial participation with your own doctor first.

Locations (2)

Princess Alexandra HospitalWoolloongabba, Queensland, AustraliaRecruiting
Australian Prostate CentreMelbourne N., Victoria, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT06956209