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

Phase 2

Recruiting

• Conditions: Pain.; Acute pain, not elsewhere classified; G89.1

• Registration Number: IRCT20121025011261N4
• Lead Sponsor: Zahedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 April 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 70

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

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

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