The effect of paracetamol ampoule and acetaminophen suppository on postoperative pain control

The effect of paracetamol ampoule and acetaminophen suppository on postoperative pain control in children admitted to pediatric surgery department

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20121025011261N4

Enrollment

Registered

2021-03-02

Start date

2021-03-05

Completion date

Unknown

Last updated

2021-04-26

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

Conditions

Pain. Acute pain, not elsewhere classified

Interventions

Intervention 1: Intervention group (1): in the group of acetaminophen suppository, the intensity of the child's pain is evaluated before the intervention. Then, according to the physician's order (PRN

Eligibility

Sex/Gender

All

Age

1 Years to 6 Years

Inclusion criteria

Inclusion criteria: Being candidate for surgery on the abdominal organ. Having the order of paracetamol ampoule and acetaminophen suppository as PRN on the patient file by physician. Have not history of acetaminophen allergy. Do not received analgesic drug in the last 4 hours.

Exclusion criteria

Exclusion criteria: Having complications such as diarrhea, vomiting, throat, and severe headache Not collaborating of child or family

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 1 hour and 2 hours after receiving analgesia medicine. Method of measurement: Toddler –preschooler postoperative pain scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlia Jalalodini

Zahedan University of Medical Sciences

a_jalalodini@yahoo.com+98 54 3344 2482

Outcome results

None listed

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