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Comparison of Positive End Expiratory Pressure Titration Methods in ARDS Patients (ELSE)

U

University Hospital, Angers

Status

Unknown

Conditions

Acute Respiratory Distress Syndrome

Treatments

Other: Strategy 2
Other: Strategy 1

Study type

Interventional

Funder types

Other

Identifiers

NCT03281473
49RC17_0220

Details and patient eligibility

About

This study aims at assessing the short-term physiological effects of 2 positive end expiratory pressure titration strategies in patients with ARDS.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age> 18 years
  • Moderate or severe ARDS
  • Consent to participation obtained from a relative

Exclusion criteria

  • Protect adult
  • Pregnant or breastfeeding woman
  • No-affiliation to the social security scheme
  • Contra-indication to the placement of an esophageal pressure measuring catheter
  • Pneumothorax
  • Hemodynamic and / or respiratory instability
  • Extra-corporeal membrane oxygenation

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Arms A
Experimental group
Description:
Strategy 1 - Washout period - Strategy 2
Treatment:
Other: Strategy 1
Other: Strategy 2
Arms B
Experimental group
Description:
Strategy 2 - Washout period - Strategy 1
Treatment:
Other: Strategy 1
Other: Strategy 2

Trial contacts and locations

1

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Central trial contact

Study Official is required by the WHO and BELONCLE, Ass.Pr

Data sourced from clinicaltrials.gov

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