Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04565795 · ClinicalTrials.gov registry record · NA

Safety and Device Performance of the Uriprene® Degradable Temporary Ureteral Stent Following Uncomplicated Ureteroscopy

A NA study of Ureteral Diseases, sponsored by Adva-Tec.

Recruiting
Registry status
NA
Development phase
87
Enrollment target
4
Study locations

NCT04565795 is a NA study of Ureteral Diseases that is actively recruiting participants, run by Adva-Tec. The registered enrollment target is 87 participants. The trial reports 4 study locations across 4 states.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04565795, a NA study of Ureteral Diseases, is actively recruiting participants, sponsored by Adva-Tec.

RECRUITING
Registry status
NA
Development phase
87 participants
Enrollment target
4
Study locations

Study Summary

A prospective, multi-center, non-randomized trial to demonstrate safety and device performance of the ADVA-Tec Uriprene® Degradable Temporary Ureteral Stent.

Conditions Studied

Interventions

  • DEVICE Uriprene® Degradable Temporary Ureteral Stent

Study Locations (4)

Arizona

  • Mayo Clinic Arizona - Phoenix

California

  • University of California Los Angeles - Los Angeles

Florida

  • University of Florida - Gainesville

Ohio

  • The Ohio State University - Columbus

Trial Details

FieldValue
Enrollment Target 87 participants
Start Date 2022-07-01
Est. Completion 2026-09
Phase NA

Sponsor

Adva-Tec

1 total trials

What the Registry Record Tells You About NCT04565795

The ClinicalTrials.gov registry entry for NCT04565795 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 87 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Adva-Tec, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Ureteral Diseases appearing as the primary indexed condition, and to 1 intervention - of which Uriprene® Degradable Temporary Ureteral Stent is the first listed.

NCT04565795 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Arizona, California, Florida.

Frequently Asked Questions

What is clinical trial NCT04565795 about?

NCT04565795 is a clinical study titled "Safety and Device Performance of the Uriprene® Degradable Temporary Ureteral Stent Following Uncomplicated Ureteroscopy". A prospective, multi-center, non-randomized trial to demonstrate safety and device performance of the ADVA-Tec Uriprene® Degradable Temporary Ureteral Stent.

What is the current status of trial NCT04565795?

This trial is currently recruiting. It is a NA study. The enrollment target is 87 participants. The study started on 2022-07-01. Estimated completion is 2026-09.

What conditions does trial NCT04565795 study?

This clinical trial studies the following conditions: Ureteral Diseases.

What interventions are being tested in trial NCT04565795?

The interventions under investigation include: Uriprene® Degradable Temporary Ureteral Stent (DEVICE).

Who is sponsoring clinical trial NCT04565795?

This trial is sponsored by Adva-Tec, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04565795 being conducted?

This trial has 4 study locations across Arizona, California, Florida, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Ureteral Diseases

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.