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Comparison between Rosemary gargle versus Lidocaine gargle on sore throat and voice violence after endotracheal intubation under general anesthesia in candidates patients for surgeries

A Comparative study of the preoperative effects of Rosemary gargle versus Lidocaine gargle on sore throat and voice violence after endotracheal intubation under general anesthesia in candidates patients for surgeries

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20101211005362N29
Enrollment
90
Registered
2022-02-26
Start date
2022-02-20
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Condition 1: Sore throat. Condition 2: Hoarseness. Pain in throat Voice and resonance disorders

Interventions

Intervention 1: Intervention group: In group1 we will give gargle of 30 drops of Rosemary solution 5% (Aboureihan company) which will be diluted with 30 drops of distilled water 2-3 minutes before gen

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Candidate patient for surgery ASA 1,2 Age between 18 to 65 years old Informed consent of patient

Exclusion criteria

Exclusion criteria: ?IV or Opioid drugs addicts Previous Allergy to drugs (Rosemary,Lidocaine) Patients with Heart,Renal pr Hepatic failure Hard Intubation (Grade 4 or upper) Malformation of airway tract

Design outcomes

Primary

MeasureTime frame
Intensity of sore throat based on VAS scale. Timepoint: Every 15 minutes at recovery, every 2 hours in first 6 hour and then at 12 and 24 hours after operation. Method of measurement: Visual Analogue Scale.;Intensity of voice violence. Timepoint: Every 15 minutes at recovery, every 2 hours in first 6 hour and then at 12 and 24 hours after operation. Method of measurement: Grade, Roughness, Breathiness, Asthenia, Strain Scale (voice disorder assessment).

Secondary

MeasureTime frame
Average satisfaction level of patients. Timepoint: First 48 hours after operation. Method of measurement: Hours count that will be measured by researcher.;Average of first time liquids regime toleration. Timepoint: First 48 hours after operation. Method of measurement: Hours count that will be measured by researcher.;Average of first time solids regime toleration. Timepoint: First 48 hours after operation. Method of measurement: Hours count that will be measured by researcher.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammadreza Safavi Homami

Esfahan University of Medical Sciences

safavi@med.mui.ac.ir009836683221

Outcome results

None listed

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