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Comparison of different doses of drugs in nebulised route to reduce airway responses during general anaesthesia technique .

Comparison of nebulised Fentanyl and different doses of nebulised Dexmedetomidine in attenuation of hemodynamic stress response to laryngoscopy and endotracheal intubation in patients undergoing nasal surgery : A randomised double blind controlled trial - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096768
Enrollment
75
Registered
2025-11-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: J342- Deviated nasal septum Health Condition 2: 8- Other Procedures Health Condition 3: H040- Dacryoadenitis Health Condition 4: J324- Chronic pansinusitis Health Condition 5: J330- Polyp of nasal cavity Health Condition 6: J343- Hypertrophy of nasal turbinates Health Condition 7: J339- Nasal polyp, unspecified Health Condition 8: J320- Chronic maxillary sinusitis Health Condition 9: J324- Chronic pansinusitis Health Condition 10: J341- Cyst and mucocele of nose and nasal sin

Interventions

Intervention1: Reducing stress response to laryngoscopy and endotracheal intubation: To compare different doses of nebulized dexmedetomidine and nebulized fentanyl in attenuation of hemodynamic stress

Sponsors

Karnataka medical college and research institute Vidyanagar Hubli
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: AMERICAN SOCIETY OF ANAESTHESIOLOGISTS [ASA]physical status classification I and II Patients undergoing elective nasal surgeries under general anaesthesia Patients giving valid informed written consent

Exclusion criteria

Exclusion criteria: Patients with neurological disorders , uncontrolled hypertension, uncontrolled Type 2 Diabetes mellitus,Ischemic heart disease, Chronic obstructive pulmonary disease, Bronchial asthma, Bleeding disorders, Psychiatric illness and nasal trauma . Patients with history of allergy to opiods and local anaesthetic agents and dexmedetomidine . Pregnant , lactating mothers. Morbidly obese patients BMI more than 40 kg / m²

Design outcomes

Primary

MeasureTime frame
To compare the effect of nebulised dexmedetomidine 1 mcg/kg ,1.5 mcg/kg and fentanyl 1 mcg/kg in attenuating hemodynamic stress response to laryngoscopy and endotracheal intubation in terms of changes in systolic blood pressure (SBP),Diastolic blood pressure (DBP),mean blood pressure (MBP)and heart rate (HR) in patients undergoing elective nasal surgeries.Timepoint: Nebulisation will be given 10min before shifting to operation theatre.

Secondary

MeasureTime frame
To assess postoperative pain using Visual Analog Scale immediately after extubation i.e 0hrand 1hr,3hr,6hr,12hr post surgery and extubationTimepoint: 0hr , 1hr, 3hr, 6hr, 12hr post surgery and extubation.;To assess postoperative Ramsay sedation score immediately after extubation i.e 0hr and 1hr, 3hr,6hr, 12hr post surgery and extubation.Timepoint: 0hr, 1hr, 3hr, 6hr, 12hr post surgery and extubation.

Countries

India

Contacts

Public ContactDR PRIYA N

KMC-RI Hubli

ladhaddharmesh@yahoo.co.in9482097491

Outcome results

None listed

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