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RECRUITING Early Phase 1

Cardiac Power Output in Cardiogenic Shock Patients

NCT05700617 · View on ClinicalTrials.gov ↗

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

846 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05700617

The ClinicalTrials.gov registry entry for NCT05700617 describes a study currently listed as recruiting. It is categorized as Early Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 846 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05700617 reports 1 study location spanning 1 distinct geographic area — top geographies include Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05700617?

The interventions under investigation include: 1:1 Randomization to receive milrinone (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05700617?

This trial is sponsored by University of Chicago, which has 846 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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