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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02027350
Other study ID # 13-008074
Secondary ID
Status Withdrawn
Phase N/A
First received December 31, 2013
Last updated November 3, 2016
Start date December 2013
Est. completion date November 2015

Study information

Verified date November 2016
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Subjects referred for right and left heart catheterization will be eligible.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
CD Leycom/Millar Instruments conductance catheter
Conductance catheter-Pressure volume relationship

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of constrictive pericarditis 1 hour No
See also
  Status Clinical Trial Phase
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