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NCT05700617 · ClinicalTrials.gov registry record · Early Phase 1

Cardiac Power Output in Cardiogenic Shock Patients

A Early Phase 1 study of Heart Failure and Cardiogenic Shock, sponsored by University of Chicago.

Recruiting
Registry status
Early Phase 1
Development phase
5
Enrollment target
1
Study location

NCT05700617 is a Early Phase 1 study of Heart Failure and Cardiogenic Shock that is actively recruiting participants, run by University of Chicago. The registered enrollment target is 5 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05700617, a Early Phase 1 study of Heart Failure and Cardiogenic Shock, is actively recruiting participants, sponsored by University of Chicago.

RECRUITING
Registry status
Early Phase 1
Development phase
5 participants
Enrollment target
1
Study location

Study Summary

The main purpose of this study is to determine whether differences in myocardial reserve predict clinical outcomes for heart failure patients.

Interventions

  • DRUG 1:1 Randomization to receive milrinone

Study Locations (1)

Illinois

  • The University of Chicago - Chicago

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2023-07-06
Est. Completion 2026-06
Phase Early Phase 1

Sponsor

University of Chicago

796 total trials

What the Registry Record Tells You About NCT05700617

The ClinicalTrials.gov registry entry for NCT05700617 describes a study currently listed as recruiting, categorized as Early Phase 1. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (100% lower). The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Heart Failure appearing as the primary indexed condition, and to 1 intervention - of which 1:1 Randomization to receive milrinone is the first listed.

NCT05700617 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT05700617 about?

NCT05700617 is a clinical study titled "Cardiac Power Output in Cardiogenic Shock Patients". The main purpose of this study is to determine whether differences in myocardial reserve predict clinical outcomes for heart failure patients.

What is the current status of trial NCT05700617?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 5 participants. The study started on 2023-07-06. Estimated completion is 2026-06.

What conditions does trial NCT05700617 study?

This clinical trial studies the following conditions: Heart Failure, Cardiogenic Shock.

What interventions are being tested in trial NCT05700617?

The interventions under investigation include: 1:1 Randomization to receive milrinone (DRUG).

Who is sponsoring clinical trial NCT05700617?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05700617 being conducted?

This trial has 1 study location across Illinois. 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

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