Brain Natriuretic Peptide (BNP) Levels in Patients in Non Invasive Mechanical Ventilation

NCT ID: NCT00453726

Last Updated: 2009-10-05

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

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-05-31

Study Completion Date

2009-07-31

Brief Summary

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The purpose of the study is to evaluate variation of BNP in non invasive mechanical ventilated patients with severe acute respiratory failure.

Detailed Description

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The aim of the study is to evaluate in patients with severe acute respiratory failure requiring non invasive mechanical ventilation BNP levels at admission and during the following 24 hours during non invasive mechanical ventilation (Non Invasive Positive Pressure Ventilation or Continuous positive airway pressure).

Because in patients affected by acute respiratory failure it is often difficult to distinguish if the disease precipitating the respiratory failure is a cardiac disease or a lung disease, aim of the present study is to evaluate the discriminating role that BNP could have in this group of patients; evaluation will be completed, once obtained clinical stabilisation, with an echocardiography and respiratory functional test.

Conditions

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Respiratory Insufficiency

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Non invasive mechanical ventilation

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Severe respiratory distress (use of respiratory accessory muscles);
* Respiratory rate \> 25 per minute;
* Respiratory acidosis (pH \< 7.35 and PaCO2 \> 45 mmHg);
* PaO2/FiO2 \< 250

Exclusion Criteria

* Age \< 18 years;
* Facial deformities;
* Pneumothorax;
* Shock or systolic arterial pressure below 90 mmHg with amine infusion;
* Life-threatening arrhythmias;
* Need for immediate endotracheal intubation (PaO2/FiO2 \< 100 with FiO2 100%, respiratory rate \< 10, GCS \< 8);
* Lack of co-operation from the patient;
* Recent esophageal-gastric surgery;
* Inability to clear secretions;
* Drugs that may interfere with BNP secretion;
* Severe obesity;
* Hepatic cirrhosis with ascitis;
* Endocrine disease.
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ospedale S. Giovanni Bosco

OTHER

Sponsor Role lead

Responsible Party

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ASL TO4 Ospedale S. Giovanni Bosco

Principal Investigators

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Giovanni Ferrari, MD

Role: PRINCIPAL_INVESTIGATOR

Ospedale San Giovanni Bosco ASL4 Torino Italy

Locations

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Ospedale San Giovanni Bosco Medicina d'Urgenza

Turin, Piedmont, Italy

Site Status

Countries

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Italy

Other Identifiers

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gbosco3

Identifier Type: -

Identifier Source: org_study_id

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