A prospective,randomized comparative study of clinical efficacy of Ambu aura gain v/s LMA proseal in adult patient undergoing elective surgery under general anaesthesia

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/06/053536

Enrollment

100

Registered

2023-06-05

Start date

Unknown

Completion date

Unknown

Last updated

2023-06-26

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

Conditions

None listed

Interventions

Intervention1: SUPRAGLOTTIC AIRWAY DEVICE insertion: group of airway devices that can be inserted into the pharynx to allow ventilation, oxygenation, and administration of anesthetic gases, without th

it protects the lungs from aspiration and the stomach from gastric insufflation

it facilitates passage of a gastric tube and monitoring devices into the esophagus

it can be inserted like the Classic or Intubating LMA

it has its own built-in bite block

malposition is detected more readily

and, through use of techniques such as gum elastic bougie-guided insertion, correct positioning is almost guaranteed.duration less than 2 hour surgery.

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade I and grade II Patients. 2. Age- 18 to 65 years of either sex. 3. Patients undergoing surgery under general anaesthesia. 4. Patient willing to give informed and written consent. 5. Mouth opening - Malampatti grade I/II. 6. Posted for surgery of short duration( <1-2hrs). 7. Posted for surgery requiring supine position only.

Exclusion criteria

Exclusion criteria: Patient refusal cervical spine pathology Anticipated difficult airway anticipated surgery greater than 3 hours

Design outcomes

Primary

Measure	Time frame
Oropharyngeal seal pressureTimepoint: Once after insertion of supraglottic airway device	—

Secondary

Measure	Time frame
Any displacement of deviceTimepoint: After extubation;Any injuryTimepoint: After extubation;Blood staining of deviceTimepoint: After extubation;Diastolic blood pressureTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;heart rateTimepoint: baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;HoarsenessTimepoint: After extubation;oxygen saturationTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;Post-op complication like sorethroatTimepoint: After extubation;Systolic blood pressureTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.	—

Measure

Time frame

Any displacement of deviceTimepoint: After extubation;Any injuryTimepoint: After extubation;Blood staining of deviceTimepoint: After extubation;Diastolic blood pressureTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;heart rateTimepoint: baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;HoarsenessTimepoint: After extubation;oxygen saturationTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.;Post-op complication like sorethroatTimepoint: After extubation;Systolic blood pressureTimepoint: Baseline,every 5 minute for initial 15 minutes and then every 15 minutes till the end of the surgery.

—

Countries

India

Contacts

Public ContactAshwani Mittal

Llrm medical college, meerut, uttar pradesh

indirayog@gmail.com9412441689

Outcome results