comparison between SLIPA and I-gel

Not yet recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2021/08/035945
• Lead Sponsor: DHINESH KUMAR C

Brief Summary

Pre anesthetic checkup will be done and thosepatients who fit into the inclusion criteria will be taken up for the study.

NPO of 6 hours for solid foods and 4 hours forliquids (prior to the procedure) will be ensured in all the patients. Theywould be pre medicated with Tab. Alprazolam 0.5 mg the night before surgeryfollowed by Inj. Pantoprazole 40 mg IV on the morning of surgery. IVaccess with 18G venflon secured in all patients. Monitors- Pulseoximeter, NIBP, ECG. ETCO2, Baseline values will be noted.

Group 1 includes the SLIPA insertion

Group 2 includes the I GEL insertion

Patients will be monitored for the following

Blood pressure and heart rate will be monitorednoninvasively.

Ease of intubation, number of attempts needed forplacement of airway, time taken for insertion, Airway leak pressure isdetermined by closing the expiratory valve of the circle system at a fixed gasflow and recording the oropharyngeal leak pressure by detection of an audiblenoise using a stethoscope placed just lateral to the thyroid cartilage.

Intra and postoperative complications if any willbe noted.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-01-09
• Last Update Posted: 2021-08-25

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 110

Inclusion Criteria

Patients aged from 18 – 60 years ASA grade I and II undergoing minor surgical procedures.

Exclusion Criteria

• Surgery extending more than 45 minutes.
• BMI ˃ 30kg/m2 Emergency procedures Pregnancy History of COPD, bronchial asthma.
• History of gastro esophageal reflux disease Â.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the heamodynamic changes such as Heart rate, systolic BP, diastolic BP, Mean arterial pressure between the two groups.	5 min, 10min, 15min, 30 min. 45 min

Secondary Outcome Measures

Name	Time	Method
to compare the ease of insertion, number of attempts and time taken	intraoperatively for 5 min , 10 min, 15min 30 MIN 45 MIN

Trial Locations

Locations (1)

OPERATION THEATRE -1, 2ND FLOOR OT COMPLEX, SHRI SATHYA SAI MEDICAL COLLEGE AND RESEARCH INSTITUTE; 🇮🇳 Kancheepuram, TAMIL NADU, India

OPERATION THEATRE -1, 2ND FLOOR OT COMPLEX, SHRI SATHYA SAI MEDICAL COLLEGE AND RESEARCH INSTITUTE

🇮🇳Kancheepuram, TAMIL NADU, India

DHINESH KUMAR C

Principal investigator

9790744463

dhinudon31@gmail.com