FindTrial
Sign In

A clinical trial to study two drug regimens, dexmedetomidine and propofol-fentanyl combination sedation for a procedure, awake fiberoptic nasotracheal intubation

A randomized clinical trial to compare the effectiveness of dexmedetomidine versus propofol-fentanyl combination for sedation during awake fiberoptic nasotracheal intubation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011417
Enrollment
60
Registered
2018-01-18
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- Difficult Airway

Interventions

Intervention1: Dexmedetomidine, Propofol-fentanyl.: Comparison of the effectiveness of sedation between dexmedetomidine and propofol-fentanyl combination during awake fiberoptic nasotracheal intubatio

Sponsors

Dr Radha M
Lead Sponsor
Dr Yatish B
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade 1 to 3 2.Patients scheduled for elective awake fiberoptic intubation.

Exclusion criteria

Exclusion criteria: 1.Baseline heart rate 2.Emergency surgery,Pregnancy Liver cirrhosis 3.Thrombocytopenia or coagulopathy contraindicating nasal intubation. 4.Known alcoholic or drug abusers,allergy to the drugs involved in the study

Design outcomes

Primary

MeasureTime frame
Intubation scores,patient tolerance scores,airway obstruction scores during awake fiberoptic intubationTimepoint: one year fourmonths—

Secondary

MeasureTime frame
Ramsay sedation scale during AFOI,number of rescue midazolam requirement and haemodynamicsTimepoint: over one year four months—

Countries

India

Contacts

Public ContactDr Radha M

M.S.Ramaiah Medical College

yatishseeni@yahoo.co.in9663093508

Outcome results

None listed

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