Analgesia-Nociception Index Guided Intraoperative Remifentanil Administration Versus Standard Practice:Evaluation of Perioperative Opioid Use

• Status: Completed
• Trial end date: 2020-03-13
• Target enrollment: 0
• Participant gender: All

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.

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

Details

• Lead Sponsor: Assistance Publique - Hôpitaux de Paris
• Treatments: Analgesics, Opioid; Remifentanil

Criteria

Inclusion Criteria:

• Elective gynecological surgery under general anesthesia

• Duration of surgery 1-7 hours

• Duration of hospital stay > 24 hours

Exclusion Criteria:

• chronic pain

• chronic analgesic medication

• neurologic disease

• psychiatric disease

• history of addiction

• kidney or liver failure

• allergy to any anesthetic or analgesic drug

• BMI > 35