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NCT05206422 · ClinicalTrials.gov registry record · NA

DORAYA-HF Early Feasibility Study

A NA study of Acute Decompensated Heart Failure, sponsored by Revamp Medical.

Active
Registry status
NA
Development phase
30
Enrollment target
14
Study locations

NCT05206422 is a NA study of Acute Decompensated Heart Failure that is active but no longer recruiting, run by Revamp Medical. The registered enrollment target is 30 participants, below the 457-participant average among 12 other Acute Decompensated Heart Failure trials with a reported enrollment target (93% lower). The trial reports 14 study locations across 8 states.

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The verdict

NCT05206422, a NA study of Acute Decompensated Heart Failure, is active but no longer recruiting, sponsored by Revamp Medical.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
14
Study locations

Study Summary

The study objective is to evaluate the feasibility of the Doraya Catheter and measure clinical performance and safety endpoints, in ADHF patients deemed to have insufficient diuretic response.

Interventions

  • DEVICE Doraya Catheter

Study Locations (14)

California

  • Zuckerberg San Francisco General - San Francisco
  • San Francisco VA - San Francisco
  • UCSF - San Francisco

Ohio

  • The Christ Hospital - Cincinnati
  • The MetroHealth System - Cleveland
  • The Ohio State University - Columbus

Georgia

  • Piedmont Hospital - Augusta
  • Northeast Georgia Medical Center - Gainesville

Texas

  • Baylor University Medical Center - Dallas
  • CHI St. Luke's Health-Baylor St. Luke's Medical Center - Houston

Florida

  • Cleveland Clinic - Weston

Missouri

  • Christian Hospital - St Louis

Oklahoma

  • Oklahoma Heart - Oklahoma City

South Carolina

  • Prisma Health - Columbia

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2022-10-05
Est. Completion 2026-03-31
Phase NA

Sponsor

Revamp Medical

2 total trials

What the Registry Record Tells You About NCT05206422

The ClinicalTrials.gov registry entry for NCT05206422 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 457-participant average among 12 other Acute Decompensated Heart Failure trials with a reported enrollment target (93% lower). The listed sponsor is Revamp Medical, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acute Decompensated Heart Failure appearing as the primary indexed condition, and to 1 intervention - of which Doraya Catheter is the first listed.

NCT05206422 reports 14 study locations spanning 8 distinct geographic areas - top geographies include California, Ohio, Georgia.

Frequently Asked Questions

What is clinical trial NCT05206422 about?

NCT05206422 is a clinical study titled "DORAYA-HF Early Feasibility Study". The study objective is to evaluate the feasibility of the Doraya Catheter and measure clinical performance and safety endpoints, in ADHF patients deemed to have insufficient diuretic response.

What is the current status of trial NCT05206422?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2022-10-05. Estimated completion is 2026-03-31.

What conditions does trial NCT05206422 study?

This clinical trial studies the following conditions: Acute Decompensated Heart Failure.

What interventions are being tested in trial NCT05206422?

The interventions under investigation include: Doraya Catheter (DEVICE).

Who is sponsoring clinical trial NCT05206422?

This trial is sponsored by Revamp Medical, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05206422 being conducted?

This trial has 14 study locations across California, Florida, Georgia, Missouri, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.