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Comparison of the effectiveness of DPI intubation procedure in comparison with conventional ITL method on improving the symptoms and overall outcome of intubation

Comparison of the effectiveness of DPI intubation procedure in comparison with conventional ITL method on improving the symptoms and overall outcome of intubation in patients prone to endotracheal intubation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200720048145N1
Enrollment
80
Registered
2020-08-11
Start date
2020-06-20
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Intubation.

Interventions

Intervention 1: Intervention group:1. we place the Laryngial Accessoris or laryngeal mask in the throat 2. Guide the catheter from the mouth to the trachea along the length of the laryngeal mask 3. Wh

Sponsors

Alborz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: The patient must need mechanical ventilation The patient must have respiratory insufficiency The patient must have severe and large chest injuries The patient should have plenty of airway discharge and need suction

Exclusion criteria

Exclusion criteria: Cardiac arrest before and during endotracheal intubation Increased ICP during endotracheal intubation Injury to the patient's mouth, jaw, and airway Spasm of the patient's vocal cords Failure to intubate the patient after two attempts

Design outcomes

Primary

MeasureTime frame
Blood pressure. Timepoint: Before and after intubation. Method of measurement: Blood pressure monitor.;Heart rate. Timepoint: Before and after intubation. Method of measurement: Monitor device.;Saturation. Timepoint: Before and after intubation. Method of measurement: Pulse oximeter.;Respiratory rate. Timepoint: Before and after intubation. Method of measurement: Ventilator device.;Glasgow Coma Scale. Timepoint: Before and after intubation. Method of measurement: Observed by the researcher.;FiO2. Timepoint: After intubation. Method of measurement: Ventilator device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Maghsoudi

Alborz University of Medical Sciences

dr.maghsoudi@abzums.ac.ir+98 26 3252 7576

Outcome results

None listed

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