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Investigating the Effect of Using the T-pieace Method among patients with head trauma

Comparing the clinical outcomes of the T-piece and pressure support ventilation among patients with head trauma: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171212037848N3
Enrollment
60
Registered
2020-04-06
Start date
2019-09-23
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Head trauma patients.

Interventions

Intervention 1: Intervention group: patients in the intervention group were placed on the T-piece for two hours. Patients who did not tolerate spontaneous breathing were reconnected to MV , were consi
otherwise, they were considered as unsuccessful weaning and placed on synchronized intermittent mandatory ventilation (SIMV). Patients with successful weaning and extubation were considered as success

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients hospitalized in intensive care units Received mechanical ventilation for at least 48 hours and at most two weeks Age of more than 18 years old Glasgow Coma Scale (GCS) score of more than 9 Normal electrolyte levels Hemoglobin greater than 8 Body temperature less than 38.5

Exclusion criteria

Exclusion criteria: chronic disease and cardiopulmonary problem intake of vasoactive medications spinal cord injury history of convulsion Poisoning-induced altered consciousness

Design outcomes

Primary

MeasureTime frame
Weaning of mechanical ventilation. Timepoint: During the hospital stay. Method of measurement: Examine the vital signs of the patient.;Extubation. Timepoint: During the hospital stay. Method of measurement: Examine the vital signs of the patient.;Duration of mechanical ventilation. Timepoint: After the weaning of mechanical ventilation. Method of measurement: Number of days the patient is under mechanical ventilation.;Length of hospital stay. Timepoint: Weaning time until hospital discharge. Method of measurement: Number of days of hospitalization.;Death rate. Timepoint: Time of death. Method of measurement: Number of deaths in two groups.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSareh Mohammadi

Qazvin University of Medical Sciences

sareh_mohammadi@ymail.com+98 28 3333 6001

Outcome results

None listed

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