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Pilot Study of Positive-End Expiratory Pressure in Acute Respiratory Distress Syndrome (PEEP-HUPA)

Primary Purpose

Respiratory Distress Syndrome, Adult

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Positive End-expiratory Pressure (PEEP)
Sponsored by
Hospital Universitario Principe de Asturias
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Distress Syndrome, Adult focused on measuring Positive-Pressure Respiration, Respiration, Artificial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with Acute Respiratory Distress Syndrome (ARDS) according to the American-European Consensus Conference definition, after 24 hours under mechanical ventilation.

Exclusion Criteria:

  • Younger than 18-year-old
  • Pregnancy
  • Neuromuscular diseases
  • Intracranial hypertension. Head trauma
  • Left ventricular dysfunction
  • Mechanical ventilation for more than 72 hours
  • Previous barotrauma
  • Patients with terminal stage of an illness and high risk of mortality within 90 days
  • Patients who refused to consent to the study

Sites / Locations

  • Critical Care Unit. Universitary Hospital Principe de Asturias

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Compliance-guided PEEP group

FiO2-driven-PEEP group

Arm Description

Positive End-Expiratory Pressure(PEEP) level was set daily, according to the method described by Suter in 1978. Static compliance (Cst) was calculated at different levels of PEEP at a constant tidal ventilation of 6-8 ml/kg of predicted body weight. Cst was determined by dividing tidal volume by the difference between the pressure at the end of inflation hold and the PEEP. The maximum value of Cst in individual patients was considered as the best PEEP.

PEEP was set based on the patient fraction of inspired oxygen (FiO2) according to the Positive End-Expiratory Pressure(PEEP) strategy reported in 2000:"Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. The Acute Respiratory Distress Syndrome Network".

Outcomes

Primary Outcome Measures

Arterial Oxygenation
Evolution of arterial oxygenation during the 28 days after study randomization

Secondary Outcome Measures

Mortality
Mortality 28 days after randomization
Number of ventilator-free days at day 28
Number of ventilator-free days at day 28 after randomization
multivariate analysis of mortality

Full Information

First Posted
May 6, 2010
Last Updated
May 7, 2010
Sponsor
Hospital Universitario Principe de Asturias
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1. Study Identification

Unique Protocol Identification Number
NCT01119872
Brief Title
Pilot Study of Positive-End Expiratory Pressure in Acute Respiratory Distress Syndrome
Acronym
PEEP-HUPA
Official Title
Randomized Controlled Pilot Study of Positive End-Expiratory Pressure (PEEP) in Acute Respiratory Distress Syndrome(ARDS): Individualized According to the Best Compliance or Fixed According to Fraction of Inspired Oxygen (FiO2) Applied
Study Type
Interventional

2. Study Status

Record Verification Date
December 2002
Overall Recruitment Status
Completed
Study Start Date
January 2003 (undefined)
Primary Completion Date
December 2007 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Hospital Universitario Principe de Asturias

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Randomized controlled pilot trial in 70 patients with Acute Respiratory Distress Syndrome (ARDS) ventilated with low tidal volumes and limitation on airway pressure at 35 centimeters of water (cmH2O), to compare two different methods of selecting the level of Positive End-Expiratory Pressure (PEEP) to be applied: according to fraction of inspired oxygen (FiO2) needed or individualized according to the best compliance. Primary objective was evolution of arterial oxygenation during the 28 days. Secondary objectives were to measure its effects on hemodynamic parameters, 28-day mortality, number of ventilator-free days at day 28, Intensive Care Unit (ICU) and hospital stay, number of multiple-organ dysfunction-free days and a multivariate analysis of 28 day-mortality.
Detailed Description
In patients with Acute Respiratory Distress Syndrome the use of Positive End-Expiratory Pressure (PEEP) avoids atelectrauma, improves gas exchange and induces alveolar recruitment.Although it has side effects as inducing alveolar overdistension and circulatory depression. There are several methods to determine the level of PEEP to be applied. We conducted a study to test the hypothesis that an individualized level of PEEP, set et the best compliance, when compared with a fixed level according to the fraction of inspired oxygen applied, improves oxygenation and reduces mortality rate at 28 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Distress Syndrome, Adult
Keywords
Positive-Pressure Respiration, Respiration, Artificial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Compliance-guided PEEP group
Arm Type
Other
Arm Description
Positive End-Expiratory Pressure(PEEP) level was set daily, according to the method described by Suter in 1978. Static compliance (Cst) was calculated at different levels of PEEP at a constant tidal ventilation of 6-8 ml/kg of predicted body weight. Cst was determined by dividing tidal volume by the difference between the pressure at the end of inflation hold and the PEEP. The maximum value of Cst in individual patients was considered as the best PEEP.
Arm Title
FiO2-driven-PEEP group
Arm Type
Other
Arm Description
PEEP was set based on the patient fraction of inspired oxygen (FiO2) according to the Positive End-Expiratory Pressure(PEEP) strategy reported in 2000:"Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. The Acute Respiratory Distress Syndrome Network".
Intervention Type
Other
Intervention Name(s)
Positive End-expiratory Pressure (PEEP)
Other Intervention Name(s)
Compliance-guided PEEP group: Grupo meseta, FiO2-driven-PEEP group: Grupo tabla
Intervention Description
All patients were ventilated during 24 hours with low tidal volume (6-8 milliliters/kilogram of predicted body weight), plateau airway pressure limited at 35 centimeters of water, initial ventilator rate of 30 breaths/minute adjusted to maintain a pH goal of 7.30 to 7.45 to a maximum of 35 breaths/minute, fraction of inspired oxygen ensuring arterial oxygen saturation 88-95% or arterial partial pressure of oxygen of 55-80 mmHg. Level of Positive End-Expiratory Pressure (PEEP) applied according the 2 arms of treatment.
Primary Outcome Measure Information:
Title
Arterial Oxygenation
Description
Evolution of arterial oxygenation during the 28 days after study randomization
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Mortality
Description
Mortality 28 days after randomization
Time Frame
28 days
Title
Number of ventilator-free days at day 28
Description
Number of ventilator-free days at day 28 after randomization
Time Frame
28 days
Title
multivariate analysis of mortality
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with Acute Respiratory Distress Syndrome (ARDS) according to the American-European Consensus Conference definition, after 24 hours under mechanical ventilation. Exclusion Criteria: Younger than 18-year-old Pregnancy Neuromuscular diseases Intracranial hypertension. Head trauma Left ventricular dysfunction Mechanical ventilation for more than 72 hours Previous barotrauma Patients with terminal stage of an illness and high risk of mortality within 90 days Patients who refused to consent to the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María del Consuelo Pintado, MD, PhD
Organizational Affiliation
Critical Care Unit. Universitary Hospital Principe de Asturias
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Raúl de Pablo, MD, PhD
Organizational Affiliation
Critical Care Unit. Universitary Hospital Principe de Asturias
Official's Role
Principal Investigator
Facility Information:
Facility Name
Critical Care Unit. Universitary Hospital Principe de Asturias
City
Alcalá de Henares
State/Province
Madrid
ZIP/Postal Code
28805
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
10793162
Citation
Acute Respiratory Distress Syndrome Network; Brower RG, Matthay MA, Morris A, Schoenfeld D, Thompson BT, Wheeler A. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med. 2000 May 4;342(18):1301-8. doi: 10.1056/NEJM200005043421801.
Results Reference
background
PubMed Identifier
340159
Citation
Suter PM, Fairley HB, Isenberg MD. Effect of tidal volume and positive end-expiratory pressure on compliance during mechanical ventilation. Chest. 1978 Feb;73(2):158-62. doi: 10.1378/chest.73.2.158.
Results Reference
background
PubMed Identifier
23362167
Citation
Pintado MC, de Pablo R, Trascasa M, Milicua JM, Rogero S, Daguerre M, Cambronero JA, Arribas I, Sanchez-Garcia M. Individualized PEEP setting in subjects with ARDS: a randomized controlled pilot study. Respir Care. 2013 Sep;58(9):1416-23. doi: 10.4187/respcare.02068. Epub 2013 Jan 29.
Results Reference
derived

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Pilot Study of Positive-End Expiratory Pressure in Acute Respiratory Distress Syndrome

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