RADA16 for Aquablation Day Case

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexMale
AgeNot listed
SponsorNYU Langone Health

About this trial

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).

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • PuraStat

Treatment groups

25 Participants
are divided into 1 treatment group

Sponsors and collaborators