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Comparison of two different supraglottic airway devices for laproscopic hernioplasty

Comparison of I-gel vs LMA Proseal as airway for laproscopic hernioplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/10/007374
Enrollment
60
Registered
2016-10-17
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

Health Condition 1: null- patients with hernia.

Interventions

Intervention1: I-gel: I-gel is a type of supraglottic airway device Control Intervention1: Proseal LMA: Proseal LMA is a type of supraglottic airway device

Sponsors

Dr Richa Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: body weight 40-60kgs

Exclusion criteria

Exclusion criteria: Obese patients,known difficult airway, mouth opening <2.5 fingers, cervical spine disease, patients prone to aspiration such as hiatus hernia and GERD and emergency surgeries. Patients with systemic illness.Those patients who does not give consent to be part of the study are excluded from the study.

Design outcomes

Primary

MeasureTime frame
a)To compare two supraglottic devices I gel vs LMA Proseal in terms of respiratory mechanics during positive pressure ventilation in laproscopic hernioplasty b)To study and compare two devices for ease of insertion and effectiveness of insertion. Timepoint: peak airway pressure, inhaled tidal volume, exhaled tidal volume, leak, minute ventilation, etco2 will be recorded 10 mins after placement of device, 10 mins after carboperitonium, 10mins after release of co2.

Secondary

MeasureTime frame
a)To study the hemodynamic parameters with the above two devices in laproscopic hernia b)Study adverse events in the group in form of trauma to airway and post operative sore throat and other complications. Timepoint: hemodynamic parameters at 1, 3,5,7,10 and 15 mins after device insertion, and after removal of device. immediate post-operative complications and delayed post-operative complications (after 12 hrs of surgery).

Countries

India

Contacts

Public ContactDr Richa Gupta

government medical collage, surat

neeta_kavishvar@yahoo.co.in9825615264

Outcome results

None listed

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