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Comparison of supraglottic airway device(AMBU AURAGAIN) versus intubating laryngeal mask airway(FASTRACH LMA) as mode for blind intubation

a new second generation supraglottic airway device(AMBU AURAGAIN)versus intubating laryngeal mask airway(FASTRACH LMA) as conduit for blind intubation-a prospective,randomized trial - SGA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050715
Enrollment
60
Registered
2023-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intubation performed with Fastrach LMA: Fastrach LMA GROUP WITH 30 Patients of ASA I AND II grade. ease of insertion of LMA and intubation time taken. Control Intervention1: AMBU AURA G

Sponsors

Dr Harjeet singh arora
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age between 18 to 60 years 2 patients with ASA grade 1 and 2 undergoing surgical procedure 3 MPG grade 1 and 2 4 BMI <35kg/m2

Exclusion criteria

Exclusion criteria: 1 Age 60 years 2 history of acid peptic disease,hiatus hernia,pregnancy 3 laryngeal pathology 4 MPG grade 3 and 4 5 ASA grade 3 and 4 6 BMI >35kg/m2

Design outcomes

Primary

MeasureTime frame
1 To study the insertion characteristics of the supraglottic device a Ease of insertion - insertion at first attempt with no resistance(easy) -difficult insertion or at second attempt(fair) -failed insertion oe insertion not possible(difficult) insertion time of individual device b Number of attempts of blind tracheal intubationTimepoint: 4 WEEKS

Secondary

MeasureTime frame
1 Hemodynamic changes(HR,SPO2) 2 Complications during insertion or removal of device(laryngospasm,blood staining,trauma to lips,teeth,tongue or posterior pharyngeal wall) after recovery from anaesthesia(sore throat,dysphagia,dysphonia)Timepoint: hemodynamic parameters will be recorded starting from baseline,1 min,2 min,3min,5min,10min interval till end of surgery

Countries

India, Indonesia, Iran (Islamic Republic of), Iraq, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Kenya, Kiribati, Kuwait, Kyrgyzstan

Contacts

Public ContactDr Harjeet Arora

government medical college amritsar

drharjeet1960@gmail.com9815005484

Outcome results

None listed

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