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

NCT07226479 · ClinicalTrials.gov registry record · NA

Non-invasive Venous Pressure Estimation

A NA study of Cardiac Intensive Care, sponsored by Yale University.

Recruiting
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT07226479: Recruiting NA study of Cardiac Intensive Care, sponsored by Yale University.

NCT07226479 is a NA study of Cardiac Intensive Care that is actively recruiting participants, run by Yale University. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07226479, a NA study of Cardiac Intensive Care, is actively recruiting participants, sponsored by Yale University.

RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The non-invasive central venous pressure estimation in adult cardiac intensive care units (CICU) patients study is a single-center, single-arm, investigator-blinded, interventional, intra-participant comparative, feasibility study. This study aims to assess the safety and preliminary accuracy of external jugular venous occlusion pressure measured non-invasively with the venous occlusion pressure monitoring device (CPMX2) in adult CICU patients. As a feasibility study, the primary goal is to gather preliminary data on the feasibility, safety, and effectiveness of the non-invasive CVP estimation method. Although single arm, the study will compare non-invasive CVP measurements with standard invasive CVP measurements taken concurrently. This intra-participant comparative approach is essential to validate the correlation and reliability of the non-invasive method.

Primary Outcome

Mean CPMX2 external jugular occlusion pressure will be compared to invasive CVP measurement in mmHg

Conditions Studied

Interventions

  • DEVICE CPMX2

Study Locations (1)

Connecticut

  • Yale New Haven Hospital CICU - New Haven

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2026-01-06
Est. Completion 2026-11
Phase NA
Yale University

1,492 total trials

What NCT07226479 shows while recruiting

NCT07226479 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Cardiac Intensive Care appearing as the primary indexed condition, and to 1 intervention - of which CPMX2 is the first listed.

NCT07226479 reports a single indexed study location in Connecticut.

Frequently Asked Questions

What is clinical trial NCT07226479 about?

NCT07226479 is a clinical study titled "Non-invasive Venous Pressure Estimation". The non-invasive central venous pressure estimation in adult cardiac intensive care units (CICU) patients study is a single-center, single-arm, investigator-blinded, interventional, intra-participant comparative, feasibility study. This study aims to assess the safety and preliminary accuracy of ext...

What is the current status of trial NCT07226479?

This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2026-01-06. Estimated completion is 2026-11.

What conditions does trial NCT07226479 study?

This clinical trial studies the following conditions: Cardiac Intensive Care.

What interventions are being tested in trial NCT07226479?

The interventions under investigation include: CPMX2 (DEVICE).

Who is sponsoring clinical trial NCT07226479?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07226479 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT07226479's enrollment target sits among peer trials

40 1448th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07226479, the US trial registry maintained by the National Library of Medicine. NCT07226479 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.