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A study comparing two medicines used for sedation during awake breathing tube insertion in patients with difficult airway, and their effect on comfort and success of the procedure.

Comparative Study Between Dexmedetomidine And Remifentanil For Optimum Intubating Conditions During Awake Fiberoptic Intubation - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107965
Enrollment
70
Registered
2026-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: Z419- Encounter for procedure for purposes other than remedying health state, unspecified

Interventions

Intervention1: Dexmedetomidine: Dexmedetomidine will be administered intravenously as a loading dose followed by continuous infusion for sedation during awake fiberoptic intubation as per the approved

Sponsors

Dr. Mouli Pundir
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged eighteen to seventy years belonging to American Society of Anesthesiologists physical status class One to Three, scheduled for surgery under general anesthesia with anticipated difficult airway and planned awake fiberoptic intubation, who are willing to participate and provide informed consent.

Exclusion criteria

Exclusion criteria: Pregnant patients, patients with history of chronic opioid use, patients receiving alpha two adrenoceptor agonists or antagonists within the previous fourteen days, patients with history of unstable angina or myocardial infarction, patients with bradycardia or heart block, and patients refusing to give consent.

Design outcomes

Primary

MeasureTime frame
Intubation success score during awake fiberoptic intubationTimepoint: Intubation success score during awake fiberoptic intubation

Secondary

MeasureTime frame
Hemodynamic parameters including heart rate blood pressure and oxygen saturationTimepoint: Baseline and every two minutes until completion of intubation;Time required for intubationTimepoint: From insertion of fiberoptic bronchoscope to confirmation of tracheal intubation;Number of intubation attempts Timepoint: During awake fiberoptic intubation;Tolerance of endotracheal tubeTimepoint: Immediately after successful intubation;Ramsay sedation scale scoreTimepoint: Baseline ten minutes after start of drug infusion and during airway anesthesia;Incidence of hypoxemia cough episodes and recall of procedureTimepoint: During intubation and at twenty four hour postoperative follow up

Countries

India

Contacts

Public ContactDr Mouli Pundir

Shri Guru Ram Rai Institute of Medical And Health Sciences

nishithgovil@rediffmail.com8126101759

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026