Mechanical Ventilation Clinical Trial
— ATCOfficial title:
Automatic Tube Compensation Versus Pressure Support in Weaning Patients With Severe Neurotoxic Snake Envenoming
In the mechanically ventilated patient, the single greatest cause of imposed work of
breathing is the resistance caused by the endotracheal tube. Commonly used maneuvers to
overcome this resistance include the use of continuous positive airway pressure or pressure
support.However, a new mode of ventilatory support called automatic tube compensation (ATC)
delivers exactly the amount of pressure necessary to overcome the resistive load imposed by
the endotracheal tube for the flow measured at the time (so called variable pressure
support).
The aim of this study is to evaluate whether a combination of pressure support with
automatic tube compensation is superior to PS alone in weaning patients with severe
neurotoxic snake envenoming.
Status | Completed |
Enrollment | 41 |
Est. completion date | April 2008 |
Est. primary completion date | December 2007 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Patients with severe neurotoxic snake envenoming (defined as requirement of mechanical ventilation for ventilatory failure) will be included in the study. - Snake envenoming will be diagnosed on the history of snakebite, presence of fang marks, presence of local manifestations such as swelling, cellulitis, blister formation; or if the dead snake is brought for identification. - Significant improvement in the neuroparalysis with improvement in grade of power to at least MRC 3 - Normal sensorium - Minimal suction requirements (less than thrice in the eight hours preceding the assessment - No requirement for any vasoactive drugs - No sedation (vi) core temperature less than 38.0°C - Hemoglobin more than 9 gm/dL (viii) systolic blood pressure more than 90 mm Hg - Overall physician assessment whether the patient is fit for weaning. Exclusion Criteria: - If they do not meet the inclusion criteria |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
India | Department of Pulmonary Medicine | Chandigarh | UT |
Lead Sponsor | Collaborator |
---|---|
Postgraduate Institute of Medical Education and Research |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration of weaning | 6 month | No | |
Secondary | ICU stay | 6 month | No |
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