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Clinical Trial Summary

This study compares two groups of patients undergoing a gynecological surgey under general anesthesia: one group in which intraoperative analgesia is guided by the Analgesia-nociception index, and another group in which intraoperative analgesia is managed as in standard practice. The objective is to assess if the Analgesia Nociception Index may result in a decrease in total analgesic drugs consumption, a decrease in post-operative pain and in chronic pain development.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03498820
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact Nada SABOURDIN, MD
Phone +33 1 71 73 89 76
Email nada.sabourdin@aphp.fr
Status Not yet recruiting
Phase N/A
Start date May 2018
Completion date May 2019

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