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Comparison of successful endotracheal intubation between the " standard-method " and " Modified-ramped position"

Comparison of successful endotracheal intubation between the " standard-method " and " Modified-ramped position"

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220511054817N1
Enrollment
112
Registered
2022-05-22
Start date
2022-05-15
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Intubation of surgical candidate patients. Failed or difficult intubation

Interventions

Intervention 1: Intervention group: In the intervention group (M), the patient is placed in a supine position on a modified RAMP (a trapezoidal device with a height of 15 cm, and a length of 80 cm, wi

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients aged between 15 and 80 years Patients with Malampati Score 2 to 4 Patients who will undergo non-emergency general anesthesia Having informed consent to participate in the study

Exclusion criteria

Exclusion criteria: Patients undergoing local or spinal anesthesia Patient dissatisfaction at any stage of the research Restriction of position in the modified ramp position History of any disease that causes instability of the cervical spine Patients with limited neck extension and flexion movement Patients with large neck masses

Design outcomes

Primary

MeasureTime frame
Duration of intubation. Timepoint: At the beginning of the study. Method of measurement: Measuring intubation time in seconds (with the help of a blind person to the type of intervention).;Number of attempts for successful intubation. Timepoint: At the beginning of the study. Method of measurement: Counting the number of times intubation (with the help of a blind person to the type of intubation intervention).;Patient satisfaction. Timepoint: 12 hours after surgery. Method of measurement: Based on the Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSourena Rezvani dehaghani

Ghoum University of Medical Sciences

Sourena1374@gmail.com+98 21 2295 2912

Outcome results

None listed

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