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NCT06948331 · ClinicalTrials.gov registry record · Phase 2

RADA16 for Aquablation Day Case

A Phase 2 study, sponsored by NYU Langone Health.

Not yet
Registry status
Phase 2
Development phase
25
Enrollment target

NCT06948331: Clinical Trial Phase 2 study, sponsored by NYU Langone Health.

NCT06948331 is a Phase 2 study that has not yet begun recruiting, run by NYU Langone Health. The registered enrollment target is 25 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06948331, a Phase 2 study, has not yet begun recruiting, sponsored by NYU Langone Health.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
25 participants
Enrollment target

Study Summary

This is a pilot proof of concept single-arm study using PuraStat following Aquablation procedure to assess reduction of hematuria to allow for same day discharge. The primary objective is to assess how PuraStat affects post-operative hematuria following Aquablation. The secondary objective is to assess the number of patients discharged on the same day based on the hematuria criteria (Grade 0 and Grade I).

Interventions

  • DEVICE PuraStat

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2026-04-01
Est. Completion 2026-08-01
Phase Phase 2
NYU Langone Health

1,164 total trials

What is known before NCT06948331 opens enrollment

NCT06948331 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 1 intervention - of which PuraStat is the first listed.

NCT06948331 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06948331 about?

NCT06948331 is a clinical study titled "RADA16 for Aquablation Day Case". This is a pilot proof of concept single-arm study using PuraStat following Aquablation procedure to assess reduction of hematuria to allow for same day discharge. The primary objective is to assess how PuraStat affects post-operative hematuria following Aquablation. The secondary objective is to a...

What is the current status of trial NCT06948331?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2026-04-01. Estimated completion is 2026-08-01.

What interventions are being tested in trial NCT06948331?

The interventions under investigation include: PuraStat (DEVICE).

Who is sponsoring clinical trial NCT06948331?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06948331's enrollment target sits among peer trials

25 1719th of 2000 higher than 245 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06948331, the US trial registry maintained by the National Library of Medicine. NCT06948331 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.