Comparison of the Effect of Propacetamol, Ibuprofen or Their Combination on Postoperative Pain and Quality of Recovery After Laparoscopic Hernia Repair in Children

• Status: Completed
• Trial end date: 2019-03-09
• Target enrollment: 0
• Participant gender: All

Summary

There are difficulties in the progress of the study and cancel the plan. The purpose of this study is to evaluate the postoperative pain control using non - opioidal analgesics in children. The investigators will investigate the effect of single use and combination of caldorol(ibuprofen) compare to denogan(propacetamol) in children.

Participants who receive the laparoscopic inguinal hernia repair between 6 months and 6 years old are divided 3 groups(caldolor, denogan, combination). Each groups are received a medication by protocol during surgery. After operation patient's pain score and use of additional analgesics are recorded in postanesthesia care unit and general ward.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Yonsei University
• Treatments: Acetaminophen; Ibuprofen; Propacetamol

Criteria

Inclusion Criteria:

• scheduled to undergo laparoscopic inguinal hernia surgery

• American Society of Anesthesiologists physical status classification 1 or 2

• Children aged 6 months to 6 years

Exclusion Criteria:

• history of Gastrointestinal bleeding

• history or laboratory finding of suspected renal or hepatic dysfunction

• bronchial asthma

• bleeding disorder

• hypersensitivity to NSAID or propacetamol

• disagreement of investigation

• The researcher determines that participation is inappropriate due to other reasons.