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Clinical Trial ● Currently Recruiting Non-phase study NCT04757116

Post-Market Study to Assess iTind Safety in Comparison to UroLift

Post-Market Study to Assess iTind Safety in Comparison to UroLift — Recruiting • Non-phase study • NCT04757116.

📅 29 Sep 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT04757116
Start
2022-09-26
Completion
2027-07-15
ClinicaliQ Trial Snapshot
  • Post-Market Study to Assess iTind Safety in Comparison to UroLift — Recruiting • Non-phase study • NCT04757116.
  • iTind and UroLift devices show similar safety and effectiveness for treating enlarged prostate symptoms in men.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The study objective is to evaluate the efficacy and safety of the iTind device compared to UroLift. Conditions: Benign Prostatic Hyperplasia (BPH) Interventions: iTind, UroLift Lead Sponsor: Olympus Corporation of the Americas Planned Enrollment: 256 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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