Prevention of Emergence Agitation in Rhinoplasty With Subanesthetic Propofol and Single-Do
To compare of prevention of emergence agitation in rhinoplasty with subanesthetic propofol and single dose dexmedetomidine
| Condition(s) | Emergence Agitation |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | To compare of prevention of emergence agitation in rhinoplasty with subanesthetic propofol and single dose dexmedetomidine |
| Who can participate | Inclusion Criteria: * Patients scheduled for rhinoplasty * Between 18-65 years * ASA I-II group Exclusion Criteria: * Those who are outside the age range of 18-65 * Those who are ASA III and above * Those with renal,hepatic, cardiac and respiratory diseases * Those with a known allergy to the medication to be used * Those who underwent urinary catheterization |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Yuzuncu Yil University |
| Locations | Van, Tuşba, Turkey (Türkiye) |
| Start date | 2025-04-15 |
| NCT ID | NCT07144007 |
| Official listing | https://clinicaltrials.gov/study/NCT07144007 |