Investigating the effect of Apotel and B complex on pain after tonsillectomy

Comparison of the preventive effect of Apotel together with venous complex with the effect of Apotel alone, on the pain of patients after tonsillectomy surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240212060979N1

Enrollment

Registered

2024-05-24

Start date

2024-06-04

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Tonsillectomy surgery. Hypertrophy of tonsils

Interventions

Intervention 1: Intervention group: The patients of the first group will receive Apotel drug at the rate of 15mg/kg along with normal saline serum (in a total volume of 100ml in microset) from 10 minu

Eligibility

Sex/Gender

All

Age

5 Years to 14 Years

Inclusion criteria

Inclusion criteria: Having inform consent ASA class 1 or 2 Children aged 5 to 14 years

Exclusion criteria

Exclusion criteria: Dissatisfaction of patients Patient with previous congenital disease Allergy to any ofdrugs used in study Patient with ASA higher than class 2

Design outcomes

Primary

Measure	Time frame
Pain level of patients after tonsillectomy surgery. Timepoint: in hours 1 (recovery section), 6, 12 and 24 hours after surgery. Method of measurement: Vas score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Abdollahzade Baghayi

Bandare-abbas University of Medical Sciences

Bagha_ar@yahoo.com+98 76 3334 5000

Outcome results

None listed

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