Skip to content

Success rate of tracheal intubation with LMAfastrach and AirQ-ILA

Comparison of success rate of tracheal intubations between two methods; the LMAfastrach and AirQ- ILA in patients undergoing elective surgery during general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20151107024909N7
Enrollment
126
Registered
2018-07-05
Start date
2016-03-20
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Airway managment. Failed or difficult intubation

Interventions

Intervention 1: Group 1: LMAfastrach, Laryngeal Mask Company, Jersey, UK, reusable, silicon. Intervention 2: Group 2: AirQ-ILA- A new device for airway establishment, re-usable silicon and plastic, Co

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Fasting Age :18-60 years Informed consent Thyromental distance more than 6 Cm Mouth opening more than two finger width Mallampati Score:1,2

Exclusion criteria

Exclusion criteria: Gastoesophageal Reflux Disease Body Mass Index more than 30 Contraindication for administration of anesthetic drugs History of difficult intubation in previous surgeries Patient Dissatisfaction

Design outcomes

Primary

MeasureTime frame
Success rate determination of tracheal intubation in LMAfastrach and AirQ-ILA groups. Timepoint: Duration of implementation of two types of supraglottic devices and tracheal intubation via supraglottic device in LMAfastrach and AirQ-ILA groups. Method of measurement: Stopwatch.

Secondary

MeasureTime frame
1-Hoarseness. Timepoint: When the patient is fully awake in recovery room. Method of measurement: By talking to patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Faranak Rokhtabnak

Iran University of Medical Sciences

rkhtbnk@yahoo.com+98 21 8894 6762

Outcome results

None listed

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