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Clinical Trial Summary

The current research is designed to investigate the analgesic efficacy of intravenous ibuprofen on the postoperative analgesic requirements, pain intensity and other recovery parameters.


Clinical Trial Description

The patients will be given general anaesthesia. Anaesthesia will be induced by propofol 1-2 mg/kg, and fentanyl 1-2 µg/kg. Endotracheal intubation will be facilitated by atracurium 0.5 mg/kg. Anaesthesia will be maintained by isoflurane in oxygen - air mixture. Transversus abdominis plane block will be performed at the end of the operation. A postoperative analgesic regimen according to group allocation will be started. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05750264
Study type Interventional
Source Menoufia University
Contact
Status Active, not recruiting
Phase Phase 2
Start date March 4, 2023
Completion date April 2024

See also
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