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Dexmedetomidine versus fentanyl for insertion of ProSeal LMA.

“A comparative study between the efficacy of a combination of dexmedetomidine with propofol versus fentanyl with propofol for insertion of ProSeal laryngeal mask airway. ?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/09/009750
Enrollment
74
Registered
2017-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

None listed

Interventions

Intervention1: ProSeal LMA insertion: Comparison of Laryngear mask airway (LMA) insertion condition using LMA insertion score in the two study groups consisting of patients undergoing elective surgica
under general anesthesia. Control Intervention1: Dexmedetomidine: Dexmedetomidine
in a dose of 1 mcg/Kg was administered intravenously over 10 minutes prior to induction of anesthesia using propofol in a dose of 2.5 mg/kg Control Intervention2: Fentanyl: Fentanyl
in a dose of 1 mcg/Kg was administered intravenously over 10 minutes prior to induction of anesthesia with propofol in a dose of 2.5 mg/kg.

Sponsors

Medica Superspecialty Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2 patients posted for Elective surgical procedures under general anaesthesia.

Exclusion criteria

Exclusion criteria: 1. Anticipated difficult airway. 2. Morbid obesity (BMI > 35). 3. Risk of gastric aspiration. 4. Patients undergoing oro – naso – pharyngeal surgeries 5. Pregnancy. 6. Those with respiratory diseases and smokers. 7. ASA grade III and IV patients. 8. Patients with bradycardia (Heart Rate less than 60beats/min) and on treatment with beta blocking agents. 9. Known sensitivity or allergy to propofol and/or dexmedetomidine and/or fentanyl. 10. Patients refusing the consent.

Design outcomes

Secondary

MeasureTime frame
To compare the effect of the two drugs on haemodynamic and respiratory parameters in such patients.Timepoint: The parameters are recorded before administration of study drug (Baseline), After administration of study drug (Pre-induction), and then after 1 minute, 3 minutes, 5 minutes, 10 minutes, 15 minutes after induction of anaesthesia with propofol.—

Primary

MeasureTime frame
To compare the efficacy of the two adjuvants, dexmedetomidine and fentanyl in combination with propofol during ProSeal LMA insertion, in selected adult patients undergoing elective surgical procedures under general anaesthesia .Timepoint: The ease of insertion of ProSeal LMA is evaluated using LMA insertion Score after 90 seconds of induction with propofol.—

Countries

India

Contacts

Public ContactAaditya Anil Prabhudesai

Medica Superspecialty Hospital

jaya20403@rediffmail.com9833138991

Outcome results

None listed

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