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Clinical Trials/IRCT20230716058799N1
IRCT20230716058799N1
Recruiting
Phase 3

Comparative study of the preemptive effect of two-different doses of intravenous dexamethasone on sore throat after caesarean section under general anesthesia

Esfahan University of Medical Sciences0 sites90 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Sore throat.
Sponsor
Esfahan University of Medical Sciences
Enrollment
90
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Pregnant women with ASA (American Society of Anesthesiologists) II older 18 years and with gestational age 37\-42 weeks who are candidate for caesarean section under general anesthesia
  • Patient's Informed consent for participate in the research study

Exclusion Criteria

  • Patients who are suflfering from a cold or sore throat before anesthesia
  • Patients with BMI more than 40
  • Use of painkiller and sedative drugs before surgery
  • Patients who have used corticosteroid during pregnancy
  • Patients who are allergic to the drug that is used in the research study
  • Patients who have asthma or lung disease in their past medical history
  • patients who have grade 3 or 4 in laryngoscopy grading (difficult intubation)

Outcomes

Primary Outcomes

Not specified

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