assessment of applying beclomethasone spray and fluticasone spray on endotracheal tube cuff on postoperative sore throat

comparative assessment of applying beclomethasone spray and fluticasone spray on endotracheal tube cuff on postoperative sore throat in elective surgery patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013012812007N2

Enrollment

Registered

2014-05-29

Start date

2014-04-01

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

Relation of applying beclomethasone spray and fluticasone spray on endotracheal tube cuff with postoperative sore throat in patient with surgery. Acute pharyngitis, unspecified

Interventions

Intervention 1: Fluticasone (200µg) spray is applied on the cuff of endotracheal tube (ETT) before intubation (flucitasone 0.05 percent or 50 mcg fluticasone in each puff made by RAHA pharmaceutical C

Treatment - Drugs

Fluticasone (200µg) spray is applied on the cuff of endotracheal tube (ETT) before intubation (flucitasone 0.05 percent or 50 mcg fluticasone in each puff made by RAHA pharmaceutical Co.)

Beclomethasone (200µg) spray is applied on the cuff of endotracheal tube (ETT) before intubation (Beclomethasone Dipropionate, spray, dose 50 µg\puff, brand CLENIL, producer SINA DAROU LAB, quantity 2

Normal saline is applied on the cuff of ETT before intubation

Eligibility

Sex/Gender

All

Age

17 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 18 to 65 year; ASA classification of I and II; having no airway problem. Exclusion criteria: patients who may be traumatized during intubation; more than two times of trying for intubation; patients who need Succinylcholine injection; taking steroid therapy; head and neck or oral surgeries; laryngoscopy time more than 15 second; patients who take analgesics for 24 hours postoperatively.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Sore throat. Timepoint: 1 and 24 hours after surgery. Method of measurement: VAS score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahareh Mirzaii

Kerman University of Medical Sciences

bahar8700@gmail.com+98 34 1322 2250

Outcome results

None listed

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