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NCT05927532 · ClinicalTrials.gov registry record · NA

Argyle Safety Fistula Cannula With Anti-reflux Valve Clinical Study

A NA study of End Stage Renal Failure on Dialysis, sponsored by Mozarc Medical US.

Completed
Registry status
NA
Development phase
40
Enrollment target
3
Study locations

NCT05927532 is a NA study of End Stage Renal Failure on Dialysis that has completed, run by Mozarc Medical US. The registered enrollment target is 40 participants, below the 270-participant average among 3 other End Stage Renal Failure on Dialysis trials with a reported enrollment target (85% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT05927532, a NA study of End Stage Renal Failure on Dialysis, has completed, sponsored by Mozarc Medical US.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target
3
Study locations

Study Summary

The purpose of the investigation is to confirm the safety and performance of the Argyle™ Safety Fistula Cannula with Anti-reflux Valve for hemodialysis treatment.

Interventions

  • DEVICE Argyle Safety Fistula Cannula with Anti-Reflux Valve

Study Locations (3)

Connecticut

  • DaVita Hartford - Hartford

Georgia

  • DaVita Columbus - Columbus

Virginia

  • DaVita Norfolk - Norfolk

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2024-03-10
Est. Completion 2024-12-15
Phase NA

Sponsor

Mozarc Medical US

1 total trials

What the Registry Record Tells You About NCT05927532

The ClinicalTrials.gov registry entry for NCT05927532 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 270-participant average among 3 other End Stage Renal Failure on Dialysis trials with a reported enrollment target (85% lower). The listed sponsor is Mozarc Medical US, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with End Stage Renal Failure on Dialysis appearing as the primary indexed condition, and to 1 intervention - of which Argyle Safety Fistula Cannula with Anti-Reflux Valve is the first listed.

NCT05927532 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Connecticut, Georgia, Virginia.

Frequently Asked Questions

What is clinical trial NCT05927532 about?

NCT05927532 is a clinical study titled "Argyle Safety Fistula Cannula With Anti-reflux Valve Clinical Study". The purpose of the investigation is to confirm the safety and performance of the Argyle™ Safety Fistula Cannula with Anti-reflux Valve for hemodialysis treatment.

What is the current status of trial NCT05927532?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2024-03-10. Estimated completion is 2024-12-15.

What conditions does trial NCT05927532 study?

This clinical trial studies the following conditions: End Stage Renal Failure on Dialysis.

What interventions are being tested in trial NCT05927532?

The interventions under investigation include: Argyle Safety Fistula Cannula with Anti-Reflux Valve (DEVICE).

Who is sponsoring clinical trial NCT05927532?

This trial is sponsored by Mozarc Medical US, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05927532 being conducted?

This trial has 3 study locations across Connecticut, Georgia, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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