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Comparision of anaesthetic drug combinations to study better relaxation

Fentanyl and propofol versus fentanyl and etomidate for the insertion conditions of laryngeal mask airway:A prospective observational study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064653
Enrollment
60
Registered
2024-03-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Fentanyl and propofol: Induction of anaesthesia will be achieved with Inj. Fentanyl @2mcg/kg+ Inj. Propofol @2mg/kg. If adequate relaxation is not achieved with initial bolus dose, an a

Sponsors

Mahatma Gandhi Memorial Medical College and Maharaja Yashwantrao Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1 and 2 Patient with planned short surgical procedures and day care surgeries (upto 1.5 hours)

Exclusion criteria

Exclusion criteria: Refusal to give consent or known allergy to any of the study drugs or Anticipated difficult airway or Relative or absolute Contraindation for laryngeal mask airway

Design outcomes

Primary

MeasureTime frame
To assess insertion condition of laryngeal mask airway in terms of number of attempts required ,time required to insert LMA, ease of insertion of LMATimepoint: Hemodynamic parameters will be recorded at baseline, after induction, at 1minute, at 3 minute, at 5 minute and there after every 5 minutes till end of surgery

Secondary

MeasureTime frame
To compare hemodynamics of two study groupsTimepoint: Hemodynamic parameters will be recorded at baseline, after induction, at 1minute, at 3 minute, at 5 minute and there after every 5 minutes till end of surgery

Countries

India

Contacts

Public ContactDr Deepali Valecha

Mahatma Gandhi Memorial Medical College, Indore

deepalisidhwani@gmail.com9424405405

Outcome results

None listed

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