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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COMPLETED
PHASE4
300 participants
INTERVENTIONAL
2015-11-30
2016-02-29
Brief Summary
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Detailed Description
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The investigator compared between the three groups regarding sore throat in intubated patients and followed them up to 48 hours.
Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
PREVENTION
SINGLE
Study Groups
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Xylocaine "X"
Patients received xylocaine gel as lubricant on endotracheal tube
xylocaine
First group were given xylocaine
Dexamethasone "D"
Patients were given dexamethasone 8 mg intravenously
Dexamethasone
Second group were given Dexamethasone
xylocaine and dexamethasone "XD"
Patients were given both xylocaine gel and dexamethasone 8 mg intravenously
Xylocaine and Dexamethasone
Third group were given both Xylocaine and Dexamethasone
Interventions
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xylocaine
First group were given xylocaine
Dexamethasone
Second group were given Dexamethasone
Xylocaine and Dexamethasone
Third group were given both Xylocaine and Dexamethasone
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Elective VS Emergency.
* Cuffed endo-tracheal tubes.
* Different types of surgery.
Exclusion Criteria
* ICU patients.
* \<15 years of age
* Laryngeal mask airway
15 Years
70 Years
ALL
No
Sponsors
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University of Jordan
OTHER
Responsible Party
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Aboud Nayef AlJabari
Regional and Cardio-thoracic anesthesia doctor
Principal Investigators
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Aboud Aljabari
Role: PRINCIPAL_INVESTIGATOR
University of Jordan
Other Identifiers
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AAlJabari
Identifier Type: -
Identifier Source: org_study_id
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