Combined Effect of Dexamethasone and Paracetamol for Postoperative Sore Throat
NCT ID: NCT02252419
Last Updated: 2014-10-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
242 participants
INTERVENTIONAL
2014-10-31
2015-03-31
Brief Summary
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Detailed Description
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The investigators want to evaluate the efficacy of the dexamethasone and paracetamol for the prevention of postoperative sore throat.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Dexamethasone
Dexamethasone will be administered 30 minutes before the anesthetic induction.
Dexamethasone
Dexamethasone will be administered.
Dexamethasone+ Paracetamol (DP)
Dexamethasone will be administered 30 minutes before the anesthetic induction. Paracetamol will be administered at the end of the surgery.
Dexamethasone
Dexamethasone will be administered.
Paracetamol
Paracetamol will be administered.
Interventions
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Dexamethasone
Dexamethasone will be administered.
Paracetamol
Paracetamol will be administered.
Eligibility Criteria
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Inclusion Criteria
* ASA I-III
Exclusion Criteria
* Patients with neck surgery
* Patients with anticipated difficult airway
* Patients with Mallampati grade 3
* Patients with severe cardiovascular or pulmonary disease
* Patients with allergic history to dexamethasone or paracetamol
* Patients with liver function disorder
* Patients with liver disease
19 Years
80 Years
ALL
No
Sponsors
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Seoul National University Hospital
OTHER
Responsible Party
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Principal Investigators
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Hee-Pyoung Park, PhD
Role: PRINCIPAL_INVESTIGATOR
Seoul National University of Hospital
Locations
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Seolu National University of Hospital
Seoul, , South Korea
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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SoreThroatParacetamol
Identifier Type: -
Identifier Source: org_study_id
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