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Effect of intravenous hydrocortisone in preventing post operative sore throat

Effect of intravenous hydrocortisone in preventing post operative sore throat followed by using laryngeal mask airway in patients undergoing urogenital surgeries

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104094005N3
Enrollment
60
Registered
2011-06-12
Start date
2009-07-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sore throat. Sore throat (acute) NOS

Interventions

Intervention 1: In intervention group, patients will be given 100 mg (2 mL) of intravenous hydrocortisone five minutes before anesthesia induction. Intervention 2: In control group, normal salin 2ml
Treatment - Drugs
In intervention group, patients will be given 100 mg (2 mL) of intravenous hydrocortisone five minutes before anesthesia induction.
In control group, normal salin 2ml will be injected 5 min before anesthesia

Sponsors

Vice chancellor for research,Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Elective urogenital surgery, ASA physical status class I-II Exclusion Criteria: Patients refuse to participate into study, Upper respiratory tract abnormalities or infection, sore throat, abdominal surgery, first unsuccessful LMA insertion, patients with full stomach, emergency conditions, pregnancy and smoking.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sore throat. Timepoint: After remove of LMA and hours 2, 4 and 24 post operative. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Blood pressure,. Timepoint: Pre and post induction-end of operation and recovery. Method of measurement: Questionnaire.;Pulse rate. Timepoint: Pre and post induction-end of operation and recovery. Method of measurement: Questionnaire.;Sao2. Timepoint: Pre and post induction-end of operation and recovery. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026