Multicenter National Randomized Controlled Open Label Study Assessing Interest of Non Invasive Ventilation in out-of Hospital Setting During Acute Respiratory Failure in Chronic Obstructive Pulmonary Disease Patients. VeNIS BPCO

Acute Respiratory Failure Clinical Trial

— VeNIS BPCO  

Official title:

Multicenter National Randomized Controlled Open Label Study Assessing Interest of Non Invasive Ventilation in out-of Hospital Setting During Acute Respiratory Failure in Chronic Obstructive Pulmonary Disease Patients. VeNIS BPCO

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT01626937
• Other study ID #: 2011-A01382-39
• Status: Not yet recruiting
• Phase: N/A
• First received: June 21, 2012
• Last updated: June 22, 2012
• Start date: June 2012
• Est. completion date: December 2014

Study information

• Verified date: January 2012
• Source: Centre Hospitalier d'Agen
• Contact: pierre-arnaud fort
• Phone: +33-0553697093
• Email: pierrearnaudf[@]yahoo.fr
• Is FDA regulated: No
• Health authority: France: Agence Nationale de Sécurité du Médicament et des produits de santé
• Study type: Interventional

Clinical Trial Summary

Goal of the study: To show that prehospital NPPV use for COPD decompensation, as compared to only standard medical treatment, might enable a decrease in intubation rate.

Primary end point: the rate of endotracheal intubation in the first three hours after randomization.

Secondary en points: rate of endotracheal intubation after third hour, rate of prehospital and ICU mortality, ICU days, effects on clinical parameters (respiratory rate, SpO2, heart rate, arterial blood pressure, consciousness) and arterial blood gases (pH, PaCO2, PaO2), 30 days mortality, delays between first medical contact and in-hospital admission, relation between initial pH level and endotracheal intubation.

Inclusion criteria: Adult patients (>18 years), with GCS≥10, known or suspected COPD and presenting acute respiratory decompensation with respiratory acidosis.

Exclusion criteria: Cardiac or respiratory arrest, upper gastro intestinal tract haemorrhage, shock, serious ventricular arrhythmia, severe sepsis, multiple organ failure, serious cranial-facial trauma, upper airways obstruction, undrained pneumothorax, uncooperative-agitated patients refusing the technique, respiratory distress with bradypnoea < 12/min, pauses gasps repeated bradycardia, intractable vomiting, acute traumatic tetraplegia, persistant hemodynamic instability with PAS<90mmHg, ensuitable environment.

Randomization: Assignment to NPPV group or standard therapy group will be performed at the time of arrival of the SAMU team to the patient, by calling a physician located at the calldispatch center who will connect to the web site of the clinical research unit from Bordeaux university hospital.

Period of study: 25 months (24 months for patients inclusion and 1 month for follow-up).

Number of patients: 199 patients in each group i.e 398 patients (significance level of 5%, power of 80%; 50% expected decrease of intubation rate, i.e. from 20 to 10%).

Main investigator: Dr Pierre-Arnaud Fort, MD, Pôle Urgences-SAMU47-Réanimation, Centre Hospitalier Saint-Esprit - Agen.

Participating centers : 20 SAMU-SMUR corresponding to 19 departments in France.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 398
• Est. completion date: December 2014
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult patients = 18 years,

• Glasgow Coma Scale (GCS) = 10,

• Written consent,

• Beneficiary social security regiment,

• Known or suspected COPD,

• Acute respiratory failure with FR > 25cycles/min,

• Setting concerned of the additional respiratory muscles and/or, paradoxical abdominal breathing,

• SpO2 < 90% with oxygen or decreasing rapidly under 90% with stop oxygen,

• PaCO2 > 45mmHg and pH < 7,35.

Exclusion Criteria:

• Cardiac or respiratory arrest,

• Upper gastro intestinal tract haemorrhage,

• Shock,

• Serious ventricular arrhythmia,

• Severe sepsis,

• Multiple organ failure,

• Serious cranial-facial trauma,

• Upper airways obstruction,

• Undrained pneumothorax,

• Uncooperative-agitated patients refusing the technique,

• Respiratory distress with bradypnoea < 12/min, pauses gasps repeated bradycardia,

• Intractable vomiting,

• Acute traumatic tetraplegia,

• Persistant hemodynamic instability with PAS<90mmHg,

• Ensuitable environment,

• Acute coronary syndrome,

• Serious acute asthma,

• Acute pulmonary edema,

• Acute respiratory insufficiency with lung before healthy,

• Gas of blood non available.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Respiratory Failure
• Exacerbation of COPD
• Lung Diseases
• Lung Diseases, Obstructive
• Non Invasive Positive Pressure Ventilation
• Out of Hospital Setting
• Pulmonary Disease, Chronic Obstructive
• Respiratory Distress Syndrome, Adult
• Respiratory Insufficiency

Intervention

Other:
• Non invasive ventilation
After nebulisation of bronchodilatators and administration of corticosteroid therapy, non invasive positive pressure ventilation will be started out of hospital and continuously in COPD patient with acute respiratory distress and respiratory acidosis, using a facial mask, with initial level of inspiratory pressure at 8 mmHg then according to VTe and/or respiratory rate; expiratory pressure at 4 mmHg then according to persistance of inspiratory work, level of FiO2 for an objective of SpO2 between 88 and 92%. In case of failure, NIV will be stopped and endotracheal intubation realized if indicate.
• conventional medical treatment
Conventional medical treatment includes nebulization of bronchodilatators every 15-20 minutes until hospital and corticosteroid therapy. If indicate during out of hospital setting, endotracheale intubation will be realized. After admission in hospital, non invasive ventilation could be started.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier d'Agen

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	rate of endotracheal intubation in the first three hours after randomization		third hour after randomization	No
Secondary	rate of endotracheal intubation after third hour		after third hour during hospitalization	No