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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00918970
Other study ID # 0708045
Secondary ID CNIL 908.476
Status Terminated
Phase N/A
First received June 8, 2009
Last updated June 12, 2009
Start date August 2008
Est. completion date June 2009

Study information

Verified date June 2009
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority France: French Data Protection Authority
Study type Observational

Clinical Trial Summary

Context: A major lack of organ donors is a serious public health problem. It determines a prolonged delay before a transplant can be performed and thus a significant number of deaths of patients waiting for transplantation. The aim of this project is to reduce the delay of the diagnosis of brain death, and also to improve its diagnosis in the Intensive Care Unit.

The diagnosis of brain death is strictly defined by the law and relies either on two consecutive flat electroencephalograms recorded at an interval of four hours, or on the lack of cerebral circulation during a brain angiography performed after suspecting brain death on the clinical exam. However, in usual practice, it is difficult to have all the needed clinical arguments, and their interpretation can be difficult in the pathological context. This may participate in the delay and the lack of patients potentially donors.

Pre-study: In a pilot study, fifty subjects with severe cerebral lesions, had a continuous ECG recording. The investigators could find that a decrease in autonomic nervous system activity, as measured through the ECG, was correlated to the transition to brain death assessed by cerebral angiography. The loss of cardiac variability was always observed between two cerebral angiographies, one before and the second after brain death. This study allowed the investigators to calculate the threshold values of sympathetic and parasympathetic activities to confirm brain death.


Description:

Aim: The aim of this second study is to validate prospectively the interest of the analysis in real-time of autonomic nervous system activity to detect brain death.

Benefits expected: Increase the number of organ donors and the number of organs removal available for transplantation.


Recruitment information / eligibility

Status Terminated
Enrollment 30
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- severe cerebral lesions

- admitted in intensive care units

Exclusion Criteria:

- neoplastic pathology

- prior myocardiac infarction

- hearth failure

- atrial fibrillation

- insulin-treated diabetes mellitus

- cardiac pacemaker

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Locations

Country Name City State
France CHU de Dijon Dijon
France CH Roanne Roanne
France CHU de Saint-Etienne Saint-etienne

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne Ministry of Health, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the delay between the falling down of autonomic nervous system activity and the confirmation of the brain death using cerebral angiography At confirmation of the brain death No
Secondary the number of patients and the number of organs removed At the end of the study No
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