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Comparison of intubation using instruments as Ambu Auragain,fastrach LMA and Blockbuster LMA.

"A Comparison Of Tracheal intubation with Ambu AuraGain, Fastrach Laryngeal Mask Airway and Blockbuster Laryngeal Mask Airway:A Prospective randomised clinical trial."

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035399
Enrollment
135
Registered
2021-08-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: H720- Central perforation of tympanic membrane Health Condition 3: H712- Cholesteatoma of mastoid Health Condition 4: K811- Chronic cholecystitis Health Condition 5: H701- Chronic mastoiditis Health Condition 6: C509- Malignant neoplasm of breast of unspecified site Health Condition 7: O- Medical and Surgical Health Condition 8: E041- Nontoxic single thyroid nodule Health Condition 9: K566- Other and unspecified intestinal obstruction Health Condition 1

Interventions

Intervention1: Tracheal intubation with supraglottic Airway devices: Comparison of tracheal intubation with Ambu AuraGain,fastrach Laryngeal Mask and Blockbuster Laryngeal Mask Airway. Control Interve

Sponsors

Department Of AnaesthesiologyRNT Medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA-I & II Scheduled for elective surgery requiring general anaesthesia and tracheal intubation.

Exclusion criteria

Exclusion criteria: Uncontrolled hypertension Cardiac disease Renal disease Hepatic disease Upper respiratory infections BMI > 30 kg/m2 Mouth opening Mallam patti grade III/IV Patient with risk of gastric aspiration

Design outcomes

Primary

MeasureTime frame
First Attempt success rate of tracheal intubation.Timepoint: During intubation

Secondary

MeasureTime frame
Ease of Laryngeal Mask Airway insertion. Oropharyngeal seal pressure Time taken for intubation Fiberoptic grade of Laryngeal view Imapct on hemodynamic variables Adverse events/Complications if anyTimepoint: From intubation to 1 hour post extubation(duration of surgery 1-4 hours)

Countries

India

Contacts

Public ContactDr Bhawesh Sharma

R.N.T Medical college,udaipur

drlalitkumar@hotmail.com9414352823

Outcome results

None listed

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