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The effect of intravenous Lidocain and Dexamethasone on post operative sore throat in general anesthesia

Comparison of the effect of intravenous Lidocain and Dexamethasone on post operative sore throat in general anesthesia with endotracheal tube: A clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017010231728N1
Enrollment
216
Registered
2017-04-07
Start date
2017-03-21
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

The effect of intravenous Lidocain and Dexamethasone on post operative sore throat in general anesthesia with endotracheal tube. Other complications of surgical and medical care, not elsewhere classified

Interventions

Intervention 1: Intervention group: Dexamethasone 0.2 mg/kg IV. Intervention 2: Intervention group: Lidocain 1mg/kg IV. Intervention 3: Control group: Distilled Water 3 cc IV.
Treatment - Drugs
Intervention group: Dexamethasone 0.2 mg/kg IV
Intervention group: Lidocain 1mg/kg IV
Control group: Distilled Water 3 cc IV

Sponsors

Deputy of research, Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients candidate for general anesthesia Exclusion criteria: ASA class 3 anesthesia risk and higher than ; emergent patients; complications of surgery and anesthesia; history of narcotic and anticonvulsant drugs use; craniofacial surgery; acute and chronic upper respiratory airways problems; non supine position

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sore throat. Timepoint: 1, 12, 24 hours after surgery. Method of measurement: Visual Analog Scale(VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahshid Mokarian

Shahroud University of Medical Sciences

mokariani@shmu.ac.ir+98 23 3239 4499

Outcome results

None listed

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