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Study will compare which drug is better for prevention of agitation occurring after awakening from anaesthesia given for nasal surgeries

Comparison between dexmedetomidine and midazolam for emergence agitation after nasal surgeries

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/03/008044
Enrollment
70
Registered
2017-03-08
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- ASA physical status I and II posted for nasal surgeries

Interventions

Intervention1: Group I - Inj dexmedetomidine: Group I would receive Inj dexmedetomidine as 0.5 mcg/kg by intravenous route over 15 minutes and then 0.1mcg/kg/hr as infusion Control Intervention1: Gr

Sponsors

Shri Sathya Sai Medical College and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Posted for nasal surgeries 2.ASA physical status I and II 3. Elective surgeries

Exclusion criteria

Exclusion criteria: 1. ASA physical status III and above 2. Heart disease and rhythm disturbances 3. psychiatric illness and anxiety disorder 4. History of post traumatic stress disorder 5. Emergency surgeries 6. Pregnancy 7. History of obstructive sleep apnea

Design outcomes

Primary

MeasureTime frame
To compare incidence of emergence agitation between Inj Dexmedetomidine and Inj Midazolam group.Timepoint: At regaining consciousness, at extubation, every 5 minutes till 30 minutes are over

Secondary

MeasureTime frame
To compare perioperative vitals, sedation and recovery profileTimepoint: At baseline, at 5 minutes, at 15 minutes after starting drug infusion then every 15 minutes till end of surgery. sedation and recovery profile at return of consciousness, at extubation and then every 5 minutes for 30 minutes.

Countries

India

Contacts

Public ContactDr Pranjali Kurhekar

Shri Sathya Sai Medical College and Research Institute

pranjalikurhekar@gmail.com04427440700

Outcome results

None listed

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