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Role of bedside ultrasound in removing artificial ventilation in patients in Intensive Care Unit

Integrated Ultrasound Protocol in predicting Weaning Success and Extubation Failure: A Prospective Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/08/015368
Enrollment
60
Registered
2018-08-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Patients on mechanically ventilation

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients consenting for the study 2. Patients mechanically ventilated for more than 48 hours. 3. All patients in being considered eligible for a half hour SBT by the attending physician

Exclusion criteria

Exclusion criteria: 1. Patients with short term mechanical ventilation in the immediate postoperative period. 2. Patients aged 3. Patients with spinal cord injury above T8 level 4. Presence of significant cardiac arrhythmia 5. Severe ICU-acquired neuromyo¬pathy 6. Patients with diaphragmatic paralysis 7. Patients planned for prophylactic noninvasive ventilation after extubation

Design outcomes

Primary

MeasureTime frame
To assess the ability of an Integrated USG protocol during weaning to predict weaning success or failure in comparison to a standard SBTTimepoint: 48 hours after extubation

Secondary

MeasureTime frame
1. To assess the ability of the Integrated USG protocol to predict SBT success or failure. 2. To assess the changes in Lung Aeration Score (LUS) during the course of a SBT. 3. To assess the changes in diaphragmatic function during the course of Mechanical ventilation 4. To assess the potential contribution of lung, diaphragmatic and cardiovascular dysfunction to failed weaning. 5. To assess the ability of the Integrated protocol to diagnose problems and guide therapy Timepoint: 48 hours after Extubation

Countries

India

Contacts

Public ContactRIDDHI KUNDU

All India Institute of Medical Sciences

drsrajeshwari@gmail.com09810079229

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026