Status:
COMPLETED
Comparison of the Effect of Propacetamol, Ibuprofen or Their Combination on Postoperative Pain and Quality of Recovery After Laparoscopic Hernia Repair in Children
Lead Sponsor:
Yonsei University
Conditions:
Inguinal Hernia
Eligibility:
All Genders
6-6 years
Phase:
NA
Brief 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 invest...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
December 15 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 9 2019
Estimated Enrollment :
159 Patients enrolled
Trial Details
Trial ID
NCT03352362
Start Date
December 15 2017
End Date
March 9 2019
Last Update
May 6 2019
Active Locations (1)
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1
Department of Anesthesiology and Pain MedicineYonsei University College of Medicine Severance Hospital
Seoul, South Korea, 03722