Bleeding and pain control outcome with topical triamcinolone in patients undergoing tonsillectomy

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241115063716N1

Enrollment

200

Registered

2025-01-18

Start date

2025-01-08

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

Tonsillectomy. Acute tonsillitis

Interventions

Intervention 1: Intervention group: For the intervention group, only one application of triamcinolone ointment will be used immediately after the end of the surgery when the patient is still unconscio

Eligibility

Sex/Gender

All

Age

7 Years to 29 Years

Inclusion criteria

Inclusion criteria: Patients without underlying disease who have undergone tonsillectomy

Exclusion criteria

Exclusion criteria: Unwillingness to participate in the study

Design outcomes

Primary

Measure	Time frame
Pain score. Timepoint: The first 6, 12, and 24 hours after tonsillectomy. Method of measurement: Visual Pain Rating Scale.;Bleeding. Timepoint: The first 6, 12, and 24 hours after tonsillectomy. Method of measurement: Examination by a surgeon.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSayyid Amir-Hossein Ghazizadeh Hashemi

Shahid Beheshti University of Medical Sciences

Amirhossainghazizadeh@sbmu.ac.ir+98 21 5102 5000

Outcome results

None listed

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