Study of Polymorphisms of RAAS and MMPs in Acute Heart Failure

NCT ID: NCT02170961

Last Updated: 2020-08-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-02-28

Study Completion Date

2016-12-31

Brief Summary

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this study aim to investigate the:

* association of RAAS polymorphisms and AHF
* association of MMP 3 and 12 polymorphisms and AHF

Detailed Description

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Heart failure can be defined as a complex clinical syndrome that results from any structural or functional disorder of the heart, with impairment of ability to fill the ventricles or eject blood. The main event of the IC is dyspnea and fatigue, which limit exercise tolerance and induces water retention.

The renin angiotensin aldosterone system governs the salt and water homeostasis in the body. Renin is a proteolytic enzyme secreted by the juxtaglomerular apparatus of the kidney (area near the glomeruli). Renin has no direct action on the organism, but that is part of the renin-angiotensin system or the renin-angiotensin-aldosterone system is known.

To date, few published studies have examined the association between the polymorphism AGT M235T \* and cardiac dysfunction; and available results are contradictory. What is not known yet is the ratio of this polymorphism with the prognosis of heart failure.

Conditions

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Acute Heart Failure

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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acute heart failure (AHF)

patients consulting the emergency department for dyspnea. the diagnosis of AHF was based on clinical, biological (BNP) and echocardiographic data.

No interventions assigned to this group

Non acute heart failure (NAHF)

patients consulting the emergency department for dyspnea. the diagnosis of AHF was based on clinical, biological (BNP) and echocardiographic data.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* aged more than 18 year old.
* acute non traumatic dyspnea .

Exclusion Criteria

* ECG diagnostic for acute myocardial infarction or ischemic chest pain within the prior 24 hours
* a history of a heart transplant, pericardial effusion, chest wall deformity suspected of causing dyspnea
* coma, shock,MV,vasopressor drugs
* arrhythmia serious and sustained,
* pace maker
* severe mitral valve disease,
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Monastir

OTHER

Sponsor Role lead

Responsible Party

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Pr. Semir Nouira

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nouira Samir, Professor

Role: PRINCIPAL_INVESTIGATOR

University of Monastir

Locations

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Nouira Samir

Monastir, Emergency Department Monastir, Tunisia 5000, Tunisia

Site Status

Countries

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Tunisia

Related Links

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Other Identifiers

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PRA-MMP

Identifier Type: -

Identifier Source: org_study_id

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