← Back to all trials
Not Yet Recruiting
NCT05634148
Dexmedetomidine in Reducing Incidence of Emergence Agitation After Nasal Surgery
Conditions: Postoperative Delirium
Sex: All
Ages: 15 Years – 70 Years
Phase: PHASE3
Enrollment: 42
Sponsor: Security Forces Hospital
Summary
Various pharmacological interventions have been attempted previously to prevent postoperative EA with variable results.
These include use of opioids, propofol, midazolam, ketamine, magnesium and alpha-2 agonists like clonidine and dexmedetomidine.
Dexmedetomidine have been used with different dosages and different timings of administration with variable results and at the expense of major hemodynamic disturbances.
The objective of this study was to investigate the role of single dose of dexmedetomidine (0.5 mcg/kg) administered as 30 minutes infusion prior to extubation in reducing the incidence and severity of EA and coughing on extubation.
Eligibility Criteria
Inclusion Criteria:We will include patients aged 15 years to 65 years, ASA 1-3 who are planned to undergo general anesthesia for elective nasal surgeries in which nasal packing is used postoperativelyExclusion Criteria:We will exclude patients with known allergy to study medications, BMI more than 35, history of obstructive sleep apnea, history of psychiatric illness, pregnancy and presence of liver and renal diseases.
Source: ClinicalTrials.gov (NCT05634148). StuddyBuddy aggregates publicly available trial information.