Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED

Regional Cerebral Oxygenation and Brain Blood Volume During Cardiac Surgery Using the NeurOS System

NCT03969836 · View on ClinicalTrials.gov ↗

Study Summary

Study of Regional Cerebral Oxygenation and Brain Blood Volume changes during Cardiac Surgery using the NeurOS system

Conditions Studied

Interventions

  • DEVICE NeurOS system

Study Locations (1)

Kentucky

  • Jewish Hospital — Louisville

Trial Details

FieldValue
Enrollment Target 113 participants
Start Date 2019-01-01
Est. Completion 2021-12-31

Sponsor

University of Louisville

260 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03969836

The ClinicalTrials.gov registry entry for NCT03969836 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 113 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Louisville, which has 260 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Heart Diseases appearing as the primary indexed condition, and to 1 intervention — of which NeurOS system 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: NCT03969836 reports 1 study location spanning 1 distinct geographic area — top geographies include Kentucky. 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 NCT03969836 about?

NCT03969836 is a clinical study titled "Regional Cerebral Oxygenation and Brain Blood Volume During Cardiac Surgery Using the NeurOS System". Study of Regional Cerebral Oxygenation and Brain Blood Volume changes during Cardiac Surgery using the NeurOS system

What is the current status of trial NCT03969836?

This trial is currently completed. The enrollment target is 113 participants. The study started on 2019-01-01. Estimated completion is 2021-12-31.

What conditions does trial NCT03969836 study?

This clinical trial studies the following conditions: Heart Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03969836?

The interventions under investigation include: NeurOS system (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03969836?

This trial is sponsored by University of Louisville, which has 260 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03969836 being conducted?

This trial has 1 study location across Kentucky. 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