Actively Recruiting

Age: 18Years +
All Genders
ID07603765

Prospective Clinical Study of Minimally Invasive Hemodynamic Monitoring Outcomes in Cardiac Ablation Procedures

Led by Istanbul University - Cerrahpasa · Updated on 2026-05-22

27

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of Pressure Recording Analytical Method (PRAM)-based minimally invasive hemodynamic monitoring during cardiac ablation procedures. This observational study focuses on adults undergoing cardiac catheter ablation, aiming to assess how this monitoring method can support management during these complex procedures, which carry risks due to arrhythmia and potential complications. The study is conducted at Istanbul University-Cerrahpa5fa Cardiology Institute and follows ethical guidelines including informed consent. Participants will receive standard monitoring such as electrocardiography, heart rate, pulse oximetry, and invasive arterial blood pressure via radial or femoral access. Alongside, continuous beat-to-beat hemodynamic data will be collected using the MostCareae system applying the PRAM algorithm. Data collection happens at three key times: before, during, and after the ablation procedure. The study focuses on various heart function parameters including cardiac output, stroke volume, and vascular resistance. During the study, participants will have continuous monitoring and multiple hemodynamic measurements taken at set intervals around the ablation. Researchers will analyze changes over time in these parameters to evaluate PRAM's role in guiding clinical decisions during the procedure. The study will also assess patient safety and generate evidence to inform future guidelines for anesthesia management in these settings. Total participation includes the ablation procedure and associated monitoring time.

CONDITIONS

Brief Title

Minimally Invasive Hemodynamic Monitoring in Cardiac Ablation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 65 18 years
  • Scheduled for cardiac catheter ablation in the electrophysiology laboratory
  • Indication for ablation confirmed by a cardiologist
  • Ability to provide written informed consent
  • Planned invasive arterial blood pressure monitoring during the procedure
Not Eligible

You will not qualify if you...

  • Refusal or inability to provide informed consent
  • Failure to identify arrhythmogenic focus leading to cancellation of ablation procedure
  • Severe hemodynamic instability prior to procedure
  • Contraindication to invasive arterial catheterization
  • Incomplete hemodynamic data acquisition
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Day of the ablation procedure

Participants undergo cardiac catheter ablation procedures with standard and minimally invasive hemodynamic monitoring.

1 procedure visit including monitoring before, during, and after ablation

Long-term Monitoring

Duration - Up to 1 day post-procedure

Participants' hemodynamic data are observed and analyzed to evaluate intra-procedural changes and clinical utility of monitoring.

Data collected at three time points: before, during, and after ablation

Trial Site Locations

Total: 1 location

1

Istanbul University-Cerrahpasa, Institute of Cardiology

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

G

GOZDE ALTUN

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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