FindTrial
Sign In

A clinical interventional trial comparing dexmedetomidine versus fentanyl along with propofol for Proseal Laryngeal mask airway insertion.The participants include Adult patients undergoing elective surgeries

Comparison of dexmedetomidine versus fentanyl co-induction with propofol for insertion of proseal laryngeal mask airway in adult patients undergoing elective surgeries - A prospective randomized double blind study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/073027
Enrollment
86
Registered
2024-08-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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: Use of drug Dexmedetomidine along with drug Propofol for Proseal laryngeal mask airway insertion: Study duration: 1 year(September 2024 - September 2025) Dexmedetomidine will be given i

Sponsors

Jeevanragul.S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and ASA 2 Patient weight between 40 to 80 kg Adult patients undergoing elective surgical procedures with general anaesthesia using Proseal laryngeal mask airway

Exclusion criteria

Exclusion criteria: Patient refusal Elective surgical procedures which need muscle relaxant ASA 3 or more Hypertensive patients Patient baseline heart rate less than 60/min BMI more than 35kg/m2

Design outcomes

Primary

MeasureTime frame
To compare dexmedetomidine against fentanyl along with propofol for optimum insertion of proseal laryngeal mask airway in adult patients undergoing elective surgeriesTimepoint: Ease of insertion of proseal laryngeal mask airway will be assessed after induction with propofol at 1 minute—

Secondary

MeasureTime frame
To compare the hemodynamic response(heart rate, Blood pressure, oxygen saturation) during insertion of proseal laryngeal mask airway. Timepoint: Heart rate,Blood pressure & Oxygen saturation will be recorded at baseline,after propofol induction, at 1, 3, 5 & 10 minutes after insertion of Proseal Laryngeal mask airway—

Countries

India

Contacts

Public ContactDr.Jeevanragul.S

Kovai Medical Center and Hospital

amarailanto@hotmail.com9486369403

Outcome results

None listed

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