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Comparison of the occurence of postoperative throat complaints after breathing tube insertion

Comparison of pharyngolaryngeal complaints after i-gel insertion with and without neuromuscular block : a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008917
Enrollment
200
Registered
2017-06-27
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- ASA I , II , III

Interventions

Intervention1: i-gel placement without neuromuscular relaxant: Patient will be induced with fentanyl and propofol and then i-gel will be inserted. Control Intervention1: i-gel insertion with neuromusc

Sponsors

Intramural funding JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -ASA I,II, II -Patients undergoing elective surgery in whom i-gel placement is planned

Exclusion criteria

Exclusion criteria: -Neuromuscular disease -Pharyngeal disease -Known case of difficult airway -Risk of aspiration -Lung pathology -BMI > 35kg/sq.m -Expected duration of surgery >3 hours -Surgeries requiring postoperative NPO status > 24 hours

Design outcomes

Primary

MeasureTime frame
Presence or absence postoperative 1. sore throat 2. foreign body sensation 3. dysphagia 4. dyshphonia 5. hoarsenessTimepoint: - 1 hour postoperative period - 24 hour postoperative period—

Secondary

MeasureTime frame
Brimacombe scoreTimepoint: after i-gel insertion;i-gel insertion parameters -insertion time -insertion attempt number -ease of insertion -ease of nasogastric tube insertion -oropharyngeal leak pressureTimepoint: During and after i-gel insertion—

Countries

India

Contacts

Public ContactM V S SATYA PRAKASH

JIPMER

munaganuri1975@yahoo.co.in9786184626

Outcome results

None listed

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