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Evaluation of effect of nebulized dexmeditomidine on attenuating the hemodynamic response to intubation during entropy targeted anaesthesia.

EVALUATION OF EFFECT OF NEBULISED DEXMEDETOMIDINE ON ATTENUATING THE HEMODYNAMIC RESPONSE TO INTUBATION DURING ENTROPY TARGETED ANAESTHESIA - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063949
Enrollment
120
Registered
2024-03-11
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: K929- Disease of digestive system, unspecified

Interventions

Intervention1: To study the effects of premedication with nebulised dexmedetomidine on blunting the haemodynamic response to laryngoscopy and tracheal intubation.: Group D: Patient will be administere

Sponsors

Department of Anaesthsia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA 1 and 2 undergoing general surgery under general anaesthesia requiring tracheal intubation.

Exclusion criteria

Exclusion criteria: 1) patients with body mass index more than 35 kg per meter square 2) patients with increased risk of aspiration of gastric contents 3) patients with airway difficulty score more than 8 4) patients with upper respiratory tract infection 5) patients with hepatic or renal insufficiency 6) patients with history of smoking or exposure to household smoke 7) patients taking medications which affect heart rate or blood pressure 8) pregnant patients.

Design outcomes

Primary

MeasureTime frame
Hemodynamic (heart rate, Blood pressure) response to laryngoscopy and tracheal intubationTimepoint: Hemodynamic (heart rate, Blood pressure) before nebulization (baseline), after nebulization, immediately after intubation, 1 minute after intubation, 5 minutes after intubation, 10 minutes after intubation, and at the end of surgery.

Secondary

MeasureTime frame
incidence of postoperative sore throat.Timepoint: at the end of surgery and 30 minutes after the end of surgery;The dose requirement of propofol for induction of anaesthesia to achieve target entropyTimepoint: prior to and during induction of anaesthesia

Countries

India

Contacts

Public ContactLakesh Kumar Anand

MM Institute of Medical Science and Research, Mullana, Ambala

lkanand11@yahoo.com9646121522

Outcome results

None listed

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