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Clinical Trials/CTRI/2020/02/023466
CTRI/2020/02/023466
Recruiting
Phase 2

Comparison of Pressure support ventilation and T-piece ventilation during spontaneous breathing trials on successful extubation among patients on mechanical ventilation.

Johnson0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: G988- Other disorders of nervous systemHealth Condition 2: T449- Poisoning by, adverse effect of and underdosing of other and unspecified drugs primarily affecting the autonomic nervous systemHealth Condition 3: J969- Respiratory failure, unspecifiedHealth Condition 4: I999- Unspecified disorder of circulatory system

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: G988- Other disorders of nervous systemHealth Condition 2: T449- Poisoning by, adverse effect of and underdosing of other and unspecified drugs primarily affecting the autonomic nervous systemHealth Condition 3: J969- Respiratory failure, unspecifiedHealth Condition 4: I999- Unspecified disorder of circulatory system
Sponsor
Johnson
Status
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
Johnson

Eligibility Criteria

Inclusion Criteria

  • •1\.Patients aged 18 years or older.
  • •2\.Patients undergoing mechanical ventilation for atleast 24 hours considered eligible for weaning by the following weaning criteria:
  • •A.Patient who are alert and co\-operative.
  • •B.The resolution or improvement of the condition leading to intubation.
  • •C.Hemodynamical stability, defined as systolic blood pressure between 90 and 160 mmHg and heart rate less than 140/min without vasopressors or with low doses of vasopressors.
  • •D.Glasgow coma scale of 8 or greater.
  • •E.Respiratory stability, defined as oxygen saturation \> 90% with FiO2 \< 0\.5, PEEP \<\= 5cm H2O, respiratory rate \< 30/min, spontaneous tidal volume \> 5mL/kg, PF ratio \> 200\.
  • •F.Non\-copious secretions ( \<3 aspirations in the last 8 hours).
  • •G.Diaphragmatic thickness fraction \> 28\.
  • •H.Rapid shallow breathing index \<\= 105\.

Exclusion Criteria

  • •1\.Pregnant women.
  • •2\.Patients with diaphragm paralysis.
  • •3\.Patients with neuromuscular disorders.
  • •4\.Patients on tracheostomy.

Outcomes

Primary Outcomes

Not specified

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