2D Strain of Right Ventricle in Peroperative of Cardiac Surgery

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Completed
CT.gov ID
NCT03298932
Collaborator
(none)
30
1
8.6
3.5

Study Details

Study Description

Brief Summary

Evaluation of the right ventricle (RV) deformation (strain) with 2D speckle tracking technics obtained by echocardiographies (TEE) in peroperative period of cardiac surgery .

TEE is performed for each patient of cardiac surgery during the operation time .

This new evaluation parameter of RV could be a good tool to assess the early RV dysfunction after cardiac surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Aortic valve surgery

Detailed Description

Monitoring of 2D strain of right ventricle free wall by TEE in perioperative of cardiac surgery :

In preoperative time After sternotomy After surgery Inclusions of patients elected for aortic valve surgery without coronary diseases or previous RV dysfunction.

Comparison with others echocardiographic parameters of RV evaluation Association with right ventricle insufficiency after cardiac surgery.

Study Design

Study Type:
Observational
Actual Enrollment :
30 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
2D Strain of Right Ventricle in Peroperative Cardiac Surgery : Evaluation of Early Signs of RV Dysfunction
Actual Study Start Date :
Sep 19, 2016
Actual Primary Completion Date :
Jan 1, 2017
Actual Study Completion Date :
Jun 7, 2017

Outcome Measures

Primary Outcome Measures

  1. 2D strain modification of right ventricle after cardiac surgery [up to 24 hours]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patient eligible for aortic valve surgery
Exclusion criteria:
  • previous right ventricle dysfunction

  • severe coronary disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital Arnaud de Villeneuve réanimation Montpellier France 34295

Sponsors and Collaborators

  • University Hospital, Montpellier

Investigators

  • Principal Investigator: Géraldine CULAS, MD, University Hospital, Montpellier

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT03298932
Other Study ID Numbers:
  • 9597
First Posted:
Oct 2, 2017
Last Update Posted:
Mar 29, 2018
Last Verified:
Oct 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by University Hospital, Montpellier
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 29, 2018