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Study to evaluate the effect of intravenous low dose Dexmedetomidine on blunting haemodynamic responses to laryngoscopy and tracheal intubation in patients undergoing surgery under general anaesthesia

Effect of intravenous low dose Dexmedetomidine on haemodynamic responses to laryngoscopy and tracheal intubation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008885
Enrollment
50
Registered
2017-06-20
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- Any patients electively posted for general anaesthesia with endotracheal intubation

Interventions

Intervention1: Dexmedetomidine: 0.5 mcg/kg Dexmedetomidine in 100ml Normal Saline over 10 minutes preoperatively Control Intervention1: Nil: Nil

Sponsors

University College of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective surgery under general anaesthesia with endotracheal intubation ASA grade 1 patients having Mallampatti grade 1 airway

Exclusion criteria

Exclusion criteria: Anticipated difficult airway History of cardiovascular, renal, respiratory, endocrine and neuronal disoders Pregnant and lactating women Patients taking any drugs affecting haemodynamic parameters.

Design outcomes

Primary

MeasureTime frame
Difference in Systolic Blood Pressure following laryngoscopy and tracheal intubation in two groups.Timepoint: 1, 3, 5, 7 and 10 minutes following laryngoscopy and tracheal intubation.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactRagesh I R

University College of Medical Sciences

drrageshir@gmail.com9205964745

Outcome results

None listed

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