Dexmedetomidine Clinical Trial
Official title:
A Comparative Study to Measure the Effect of Nebulized Dexmedetomidine - Lidocaine for Controlling Postoperative Pain After Tonsillectomy in Adults.
A comparative study to measure the effect of nebulized dexmedetomidine - lidocaine for controlling postoperative pain after tonsillectomy in adults.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | April 15, 2022 |
Est. primary completion date | April 10, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Patients of either sex, aged between 18-30 years old, ASA physical status I, II undergoing tonsillectomy. Exclusion Criteria: - Patients were excluded if they had clinically important coronary atherosclerotic heart disease, a history of stroke or transient ischemic attack, Sinus bradycardia or heart block, coagulopathy, peritonsillar abscess, any infection at the site of injection, Known allergy to the study drugs (lidocaine, dexmedetomidine). |
Country | Name | City | State |
---|---|---|---|
Egypt | Cairo university hospitals | Cairo |
Lead Sponsor | Collaborator |
---|---|
Kasr El Aini Hospital |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Postoperative pain 4 hours after tonsillectomy measured by visual analogue score | 4 hours postoperative | ||
Secondary | Postoperative nausea and vomiting following tonsillectomy operation after1 hour , 2 hours and after 4 hours | 4 hours postoperative |
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