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A randomized clinical trial comparing spontaneous breathing trials using either T-piece or pressure support ventilation as a modality of ventilator withdrawal.

Comparison between spontaneous breathing trials with T-piece or pressure support ventilation as ventilator weaning modality: a randomized clinical trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/078923
Enrollment
70
Registered
2025-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Spontaneous Breathing Trial with T piece.: T-piece at oxygen flow rate of up to 6 litter per minute.Fio2 of 40% or lower.Performed for approximately 1 hour. Control Intervention1: Spont

Sponsors

The Institute of Post Graduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Fulfilled weaning criteria. 2 Spontaneous breathing trial completed

Exclusion criteria

Exclusion criteria: 1 Traumatic Brain injury. 2 Pre-existing peripheral neuromascular disease. 3 Do not reintubate order at the time of the initial spontaneous breathing trial.

Design outcomes

Primary

MeasureTime frame
Total time without exposure to invasive ventilation at 72 hours after the initial spontaneous breathing trial.Timepoint: 12 month—

Secondary

MeasureTime frame
Re-intubation rate at 72 hours after the initial spontaneous breathing trial.Timepoint: 12 month—

Countries

India

Contacts

Public ContactTathagata Dewasi

Institute Of Post Graduate Medical Education and Research Kolkata

rajat.choudhuri@gmail.com9874660960

Outcome results

None listed

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