Monitoring Analgesia by ANI (Analgesia The Nociception Index)
Not Applicable
Completed
- Conditions
- Surgical Procedure, UnspecifiedNociceptive Pain
- Interventions
- Device: ANI monitor
- Registration Number
- NCT03749304
- Lead Sponsor
- University Hospital, Lille
- Brief Summary
The objective of this research is to study the variations of the ANI(Analgesia The Nociception Index) according to 2 periods: the "NoStim" period before surgical incision under general anesthesia and the period of hemodynamic reactivity "ReactHemo" peroperative. This period is defined by a 20% increase in FC and / or PAS (the only gold standard today).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
- patient with IBD
- Scheduled surgery: laparotomy or laparoscopic resection with high risk of laparo-conversion
Exclusion Criteria
- patient included in another current study or the previous month
- urgent surgery
- toxicomania or receiving opioids preoperatively
- pregnant woman
- psychosis
- betablocker treatment
- diabetic dysautonomia
- non-sinus heart rate
- pacemaker heart transplant
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description ANI monitor ANI monitor -
- Primary Outcome Measures
Name Time Method Change of ANI greater than 20 points During the surgery, an average Three hours and a half ANI decrease greater than 20 points between a "NoStim" period before surgical incision under general anesthesia and a period of intraoperative "ReactHemo" hemodynamic reactivity defined by a 20% increase in FC and / or PAS.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hôpital Claude Huriez, CHU
🇫🇷Lille, France