Overview

The recruitment status of this trial is unknown because the information has not been verified recently.

Condition constrictive pericarditis
Treatment cd leycom/millar instruments conductance catheter
Sponsor Mayo Clinic
Start date December 2013
End date November 2015
Trial size 0 participants
Trial identifier NCT02027350, 13-008074

Summary

Until now, diagnosis of constriction was based on pressure changes of ventricle by conventional pressure-wide hemodynamic evaluation but not on ventricular volume change. This study will provide answers to persisting questions about volume changes during respiration in patients with constrictive pericarditis by directly measuring both right and left ventricular volume.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification efficacy study
Intervention model single group assignment
Masking open label
Primary purpose diagnostic
Arm
(Experimental)
Changes in pressure-volume relationships will be compared to changes in LV and RV systolic pressure during respiration.
cd leycom/millar instruments conductance catheter
Conductance catheter-Pressure volume relationship

Primary Outcomes

Measure
Presence of constrictive pericarditis
time frame: 1 hour

Eligibility Criteria

Male or female participants at least 18 years old.

Subjects referred for right and left heart catheterization will be eligible.

Additional Information

Official title Pressure-Volume Analysis of Constrictive Pericarditis
Principal investigator Barry Borlaug, MD
Trial information was received from ClinicalTrials.gov and was last updated in November 2016.
Information provided to ClinicalTrials.gov by Mayo Clinic.