PACTR202310783988259

Does intravenous lidocaine associated with spinal anesthesia reduce post-operative pain after C-Section? The i-Lido-CA Trial

i-Lido-CA Trial: Intravenous Lidocaine for Cesarean Analgesia
Syrine Aguir·Phase 4·Pan Africa Clinical Trials Registry·drugNot yet recruiting
Study focus
Disease/Condition
Surgery; Anaesthesia
Intervention type
drug
Sponsor & location
Primary sponsor
Syrine Aguir
Location
Tunisia
Timeline & enrollment
Phase
Phase 4
Start date
Jan 01, 1900
End date
Jan 01, 1900
Summary

Postoperative pain associated with Cesarean sections has significant socioeconomic implications, including potential risks of chronic pain and postpartum depression. Effective pain management improves recovery and maternal well-being, especially in Enhanced Recovery After Cesarean Surgery (ERACS). Spinal anesthesia is commonly used for cesarean sections, but it can lead to side effects such as nausea and vomiting. The management of postoperative pain involves multimodal analgesia, such as intrathecal opioids and non-opioid analgesics. To address these issues and enhance postoperative recovery, various medications and techniques have been explored, including intravenous lidocaine. We aim in this research study to evaluate the analgesic and hemodynamic benefits of intravenous lidocaine for cesarean section under spinal anesthesia.

ICD-10 classifications
Other complications of anaesthesiaAnaesthetic, unspecifiedDuring surgical operationDuring surgical operationDuring surgical operation
Data source
Registry
Pan Africa Clinical Trials Registry
Trial ID
PACTR202310783988259
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for PACTR202310783988259 through Pure Global AI's free database. This Phase 4 trial is sponsored by Syrine Aguir and is currently Not yet recruiting. The study focuses on Surgery; Anaesthesia.

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