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Clinical Trials/CTRI/2021/03/032431
CTRI/2021/03/032431
Not yet recruiting
Phase 3

COMPARATIVE EVALUATION OF TRANSPULMONARY PRESSURE GUIDED VENTILATION VERSUS CONVENTIONAL VENTILATION IN PATIENTS WITH A.R.D.S

self0 sites0 target enrollmentTBD
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Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
self
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
self

Eligibility Criteria

Inclusion Criteria

  • •Patients will be included in the study if they have moderate\-to\-severe ARDS according to the American\-European Consensus Conference definitions.
  • •Duration of ARDS 36 hours or less from meeting final Berlin criterion
  • •Age more than 18 years.

Exclusion Criteria

  • •Received mechanical ventilation more than 96â??h.
  • •Recently treated for bleeding varices, stricture, haematemesis, esophageal trauma, recent esophageal surgery or other contraindication for nasogastric tube placement.
  • •History of lung or liver transplantation.
  • •Severe chronic liver disease (Child\-Pugh Score \>\=12\).
  • •Patients not committed to full support.
  • •Inability to get informed consent from the patient or surrogate.
  • •Use of rescue therapies prior to enrolment (including nitric oxide, ECMO, prone positioning)
  • •Evidence of active air leak from the lung (including bronchopleural fistula, pneumothorax, pneumomediastinum or air leak from existing chest tube).

Outcomes

Primary Outcomes

Not specified

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