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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02856607
Other study ID # RC12_3675
Secondary ID
Status Recruiting
Phase N/A
First received August 2, 2016
Last updated August 2, 2016
Start date February 2014
Est. completion date December 2018

Study information

Verified date August 2016
Source Assistance Publique Hopitaux De Marseille
Contact Gilbert HABIB
Phone 04 91 38 75 87
Email gilbert.habib@ap-hm.fr
Is FDA regulated No
Health authority France: Comité consultatif sur le traitement de l'information en matière de recherche dans le domaine de la santé
Study type Observational

Clinical Trial Summary

Infective endocarditis (IE) is defined as a bacterial infection of the endocardium (inner surface of the heart), which may include one or more heart valves. Epidemiologic pattern has changed during the last 20 years whereas the incidence was unchanged. However, the mortality increase despite recent diagnosis and therapeutic advances.

Only few investigations consider the prognostic and the therapeutic medical care according to the clinical care pathway. In fact, 3 situations are observed: (i) patient for whom diagnosis and medical care are realized in a referent center with cardiac surgery, (ii) patients secondary addressed to a referent center with cardiac surgery, (iii) patients for which the totality medical care are performed in non-referent health center. In addition, epidemiologic studies concern only a part of IE, not including most of the time the patients hospitalized in non-referent center.

The aim of the study was to determine the prognosis of threated patients according to the clinical care pathway. Secondary objectives was (i) to evaluate the application of European recommendations concerning trans-oesophageal echocardiogram (TOE), antibiotic treatment and surgical practice, (ii) to compare the epidemiologic profile according to the type of center.

For this, 300 patients addressed in the 22 French participating centers for a possible or certain IE according to Duke Criteria were prospectively included during 3 years.

Patient data (clinical, demographical, biological, microbiological, echocardiographic and evolutive data) were collected at the admission, during hospitalization, at discharge and one-year follow up.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 2018
Est. primary completion date February 2018
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- adult with infective endocarditis episode according to Duke Criteria

Exclusion Criteria:

- Patients with a new episode of infective endocarditis that led to its prior inclusion in the study

Study Design

Time Perspective: Prospective


Intervention

Other:
determine the prognosis of threated patients according to the clinical care pathway.


Locations

Country Name City State
France Assistance Publique Hôpoitaux de Marseille Hôpital de la Timone Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the all-cause one-year mortality according to the group one year No
Secondary the application of European recommendations realization of trans-oesophageal echocardiogram (TOE) one year No
Secondary antibiotic treatment type and time of antibiotic treatment for common germ, one year No
Secondary surgery performing valve surgery and / or total extraction of an implanted pacemaker or defibrillator. one year No
See also
  Status Clinical Trial Phase
Completed NCT02816307 - Etiology of Endocarditis in Negative Blood Cultures N/A