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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02384252
Other study ID # 2012_09
Secondary ID 2012-A01605-38
Status Completed
Phase
First received
Last updated
Start date June 3, 2013
Est. completion date January 19, 2017

Study information

Verified date July 2019
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators aim to explore obese cardiomyopathy by studying contractile twitch force, sarcomere sensitivity to calcium and mitochondrial function in atrial myocardial samples of patients grouped according to their body mass index, i.e. normal weight, overweight and obese.


Description:

Obesity is associated with the development of heart failure, regardless of coronary artery disease or other comorbidities.

Right atrial samples obtained from patients undergoing cardiac surgery and presenting no sign of clinical cardiomyopathy will be grouped according to patient's body mass index. Atrial trabeculae will be explored to dissect out the respective contribution of (i) sarcoplasmic reticulum dysfunction (isometric twitch force contraction analysis), (ii) abnormal sarcomere sensitivity to calcium assessed in permeabilized fibers and (iii) mitochondrial dysfunction to intrinsec contractile dysfunction of myocardium in obese patients.


Recruitment information / eligibility

Status Completed
Enrollment 134
Est. completion date January 19, 2017
Est. primary completion date January 19, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient schedulled for coronary artery bypass graft surgery or aortic valve replacement surgery with extracorporeal circulation

- must be over 18 years of age

- must be able to read and understand the consent form in French

- must be in sinus rhythm at inclusion time

Exclusion Criteria:

- medical history of type 1 diabetes

- medical history of sustained atrial arrhythmia

- pregnancy

- class III anti-arhythmic drug

Study Design


Related Conditions & MeSH terms


Intervention

Other:
functional tissu atrial analysis


Locations

Country Name City State
France Hôpital Cardiologique - EFCV - CHRU Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intrinsic myocardial contractile force twitch force developed by atrial trabeculae assessed in isometric conditions in atrial samples the day of cardiac surgery
Secondary sarcomere sensitivity to calcium force-calcium concentration relation assessed on permeabilized atrial fibers the day of cardiac surgery
Secondary Mitochondrial function assesment of mitochondrial respiration and calcium retention capacity by oxygraphic measurement in saponin-permeabilized atrial fibers the day of cardiac surgery
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