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Speckle-tracking Tricuspid Annular Plane Systolic Excursion

University of Nebraska logo

University of Nebraska

Status

Completed

Conditions

Ventricular Function, Right

Treatments

Other: Concurrent TTE and TEE

Study type

Observational

Funder types

Other

Identifiers

NCT01968252
0107-14-EP

Details and patient eligibility

About

The study is designed to validate the use of speckle-tracking echocardiography to measure tricuspid annular plane systolic excursion as a measurement of right ventricular function during transesophageal echocardiography.

Full description

  1. Use of speckle-tracking echocardiography to validate tricuspid annular plane systolic excursion measurements with transesophageal echocardiography.
  2. This study intends to validate the use of speckle-tracking echocardiography to measure the distance the tricuspid annulus moves during the systolic phase. The guideline articles regarding right ventricular function suggest m-mode measurements from the transthoracic approach and the same measurements may underestimate the actual distance on transesophageal echocardiography. This speckle-tracking technology will allow this distance to be measured despite its often non-parallel motion to the ultrasound beam, which otherwise limits the reliability of the valve recorded.
  3. All subjects undergoing a planned surgical procedure in which the use of transesophageal echocardiography would be used regardless for their management.
  4. No interventions, only evaluation of the measurements obtained with transthoracic echocardiography compared to transesophageal echocardiography.
  5. No follow-up, study will be completed at the time of image acquisition.

Enrollment

112 patients

Sex

All

Ages

19 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All subjects who are scheduled to undergo general anesthesia and concurrently will be managed with intraoperative transesophageal echocardiography will be included in potential subjects.

Exclusion criteria

  • Subjects who do not have adequate transesophageal and/or transthoracic imaging windows to allow for accurate analysis of tricuspid annular motion.

Trial design

112 participants in 1 patient group

Intraoperative Patient
Description:
All patients in the cohort will be scheduled to undergo a planned surgical procedure in which the subject will undergo general anesthesia and the procedure and/or the patient will require transesophageal echocardiographic monitoring for the procedure.
Treatment:
Other: Concurrent TTE and TEE

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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