Skip to content

To compare 3 supraglottic airways in pediatric population undergoing lower abdomen surgery

To compare oropharyngeal leak pressure and ease of insertion between Ambu AuraGain, Proseal LMA, and I-gel in infants and pediatric patient posted for lower abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013470
Enrollment
90
Registered
2018-04-25
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: null- Children (both male and female) of age between 1 to 10 years, who are to undergo elective abdominal surgery of less than 4 hours duration, with ASA class 1 and 2 will be included.

Interventions

Intervention1: Ambu AuraGain, i-gel and Proseal LMA for airway management: Ambu AuraGain, i-gel,Proseal LMA will be used to secure airway in pediatric patients undergoing routine lower abdomen surgery

Sponsors

Dr RPGMC Kangra at Tanda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children (both male and female). Of age,between 1 to 10 years. who are to undergo elective abdominal surgery of With ASA class 1 and 2.

Exclusion criteria

Exclusion criteria: Patient with expected difficult airway (including mouth opening At risk of aspiration (full stomach patient). ASA class 3 and 4. With upper respiratory tract infection or with coagulopathy.

Design outcomes

Primary

MeasureTime frame
1. To compare oropharyngeal leak pressure and leak fraction between Ambu AuraGain, Proseal LMA and i-gel. 2. To compare CL grade through different devices using paediatric fiber-optic scope. Timepoint: afer 10 min of securing supraglottic airway, followed by every 30 min till complition of surgery.

Secondary

MeasureTime frame
1.To compare time of insertion, ease of insertion of device, insertion of orogastric tube, number of attempts and ease of removal of the device. 2.Laryngopharyngeal morbidity in form of trauma to lips, teeth and gum and blood stain on device will be noted. Timepoint: during insertion and removal

Countries

India

Contacts

Public ContactDr Sudarshan Kumar

Dr. R.P.G.M.C., Tanda

sudarshan_58@rediffmail.com9418086604

Outcome results

None listed

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