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Completed Not applicable Interventional

DORAYA-HF Early Feasibility Study

ClinicalTrials.gov ID: NCT05206422

Public ClinicalTrials.gov record NCT05206422. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 9:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

DORAYA-HF: Assessment of the Doraya Catheter for the Treatment of Volume Overload in Acute Heart Failure Patients With Insufficient Response to Diuretics

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT05206422
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Revamp Medical Inc.
Industry
Enrollment
21 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 5, 2022 (Actual)
Primary completion
Jan 31, 2026 (Actual)
Completion
Jan 31, 2026 (Actual)
Last update posted
Aug 13, 2026

2022 – 2026

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Zuckerberg San Francisco General San Francisco California 94110 —
San Francisco VA San Francisco California 94121 —
UCSF San Francisco California 94143 —
Cleveland Clinic Weston Florida 33331 —
Piedmont Hospital Augusta Georgia 30901 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Christian Hospital St Louis Missouri 63136 —
The Christ Hospital Cincinnati Ohio 45219 —
The MetroHealth System Cleveland Ohio 44109 —
The Ohio State University Columbus Ohio 43210 —
Oklahoma Heart Oklahoma City Oklahoma 73135 —
Prisma Health Columbia South Carolina 29203 —
Baylor University Medical Center Dallas Texas 75246 —
CHI St. Luke's Health-Baylor St. Luke's Medical Center Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05206422, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 13, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05206422 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →