Intraoperative Fentanyl Consumption Guided by Analgesia Nociception Index
Primary Purpose
Postoperative Pain, Postoperative Complications
Status
Completed
Phase
Not Applicable
Locations
Thailand
Study Type
Interventional
Intervention
Standard protocol
ANI protocol
Sponsored by
About this trial
This is an interventional treatment trial for Postoperative Pain
Eligibility Criteria
Inclusion Criteria:
- Adults female undergoing elective breast surgery
- American Society of Anesthesiologists (ASA) classification I-III
- Body mass index (BMI) 18.5-35 kg/m2
Exclusion Criteria:
- Implanted pacemaker
- Cardiac arrythmia
- Autonomic nervous system (ANS) disorder, e.g. epilepsy, stroke
- Chronic opioid use
- Chronic pain
- On beta-blocker, calcium channel blocker, or other drugs to control arrythmia
- Previous mastectomy
- Pregnancy
- On Nsaids
Sites / Locations
- Srinagarind Hospital, Faculty of Medicine, Khon Kaen University
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Control group
ANI group
Arm Description
Intraoperative fentanyl administration will be guided by standard protocol
Intraoperative fentanyl administration will be guided by ANI protocol
Outcomes
Primary Outcome Measures
Postoperative pain: NRS
Measure pain numeric rating scale (NRS) every 15 minutes. NRS has a range from 0 to 10 with 0 indicates no pain while 10 indicates worst pain. NRS of 0-3 is mild, 4-6 is moderate, and 7-10 is severe pain.
Secondary Outcome Measures
Intraoperative fentanyl consumption
Cumulative fentanyl used intraoperatively of both groups
Intraoperative ANI score
Intraoperative ANI score of both groups. ANI has a range from 0 to 100 with 0 indicates worst pain while 100 indicates no pain. ANI 0-49 suggests that more opioid is needed. ANI 50-70 indicate optimal analgesic and no opioid is needed. ANI > 70 indicates excessive effect of opioid and opioid should be withheld.
Postoperative nausea/vomiting
Nausea/vomiting score (PONV score) every 4 hours. PONV score has a range of 0 to 3. N/V scores 0= none, 1= mild, 2= moderate, and 3= severe PONV.
Postoperative sedation score
Sedation score every 4 hours. Sedation score has a range of 0 to 3 with 0= fully alert, 1= mild sedation, easy to rouse, 2= moderate sedation, arousable with gentle shaking, and 3= deep sedation, not aroused by speaking or gentle shaking.
Full Information
NCT ID
NCT03716453
First Posted
October 21, 2018
Last Updated
November 25, 2019
Sponsor
Khon Kaen University
1. Study Identification
Unique Protocol Identification Number
NCT03716453
Brief Title
Intraoperative Fentanyl Consumption Guided by Analgesia Nociception Index
Official Title
A Comparative Study of Intraoperative Fentanyl Consumption Guided by Analgesia Nociception Index Versus Standard Protocol in Patients Undergoing Mastectomy
Study Type
Interventional
2. Study Status
Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
May 31, 2019 (Actual)
Study Completion Date
August 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Khon Kaen University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Balanced anesthesia needs optimization of hypnotic, relaxant, and narcotic. Administration of hypnotic drugs can be monitored by bispectral index score (BIS), while the dosage of muscle relaxants can be guided by train-of four (TOF). However, administration of narcotics lacks objective monitor. Overdosage of narcotic may lead to delayed awakening, while underdosage may lead to high degree of postoperative pain. Recently, there is a monitor, Analgesic Nociceptive Index (ANI) monitor, designed to guide the administration of narcotics. There are many descriptive studies supporting the correlation of ANI score and pain score but there are still very few randomized control studies which report the efficacy of ANI in clinical practice.
Detailed Description
Objective: To evaluate the efficacy of ANI to guide the administration of intraoperative fentanyl.
Methods: Sixty female patients undergoing breast surgery with balanced anesthesia will be randomized into 2 groups. The first group will receive fentanyl according to standard practice of attending anesthesiologists. The second group will receive fentanyl according to ANI score protocol.
Primary outcome: Postoperative pain numeric rating scale (NRS) score during 60 minutes in postanesthetic care unit (PACU).
Secondary outcomes: Total intraoperative dose of fentanyl and postoperative nausea/vomiting and sedation score in PACU.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain, Postoperative Complications
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Intraoperative fentanyl administration will be guided by standard protocol
Arm Title
ANI group
Arm Type
Experimental
Arm Description
Intraoperative fentanyl administration will be guided by ANI protocol
Intervention Type
Procedure
Intervention Name(s)
Standard protocol
Intervention Description
Give narcotic according to vital signs
Intervention Type
Procedure
Intervention Name(s)
ANI protocol
Intervention Description
ANI score 50-70 indicates optimal narcotic effect. ANI score > 70 indicated overdosage of narcotic and narcotic should be withheld.
ANI score < 50 indicates inadequate narcotic and narcotic should be given.
Primary Outcome Measure Information:
Title
Postoperative pain: NRS
Description
Measure pain numeric rating scale (NRS) every 15 minutes. NRS has a range from 0 to 10 with 0 indicates no pain while 10 indicates worst pain. NRS of 0-3 is mild, 4-6 is moderate, and 7-10 is severe pain.
Time Frame
during 60 minutes in PACU
Secondary Outcome Measure Information:
Title
Intraoperative fentanyl consumption
Description
Cumulative fentanyl used intraoperatively of both groups
Time Frame
During intraoperative period
Title
Intraoperative ANI score
Description
Intraoperative ANI score of both groups. ANI has a range from 0 to 100 with 0 indicates worst pain while 100 indicates no pain. ANI 0-49 suggests that more opioid is needed. ANI 50-70 indicate optimal analgesic and no opioid is needed. ANI > 70 indicates excessive effect of opioid and opioid should be withheld.
Time Frame
During intraoperative period
Title
Postoperative nausea/vomiting
Description
Nausea/vomiting score (PONV score) every 4 hours. PONV score has a range of 0 to 3. N/V scores 0= none, 1= mild, 2= moderate, and 3= severe PONV.
Time Frame
During 24 hours postoperatively
Title
Postoperative sedation score
Description
Sedation score every 4 hours. Sedation score has a range of 0 to 3 with 0= fully alert, 1= mild sedation, easy to rouse, 2= moderate sedation, arousable with gentle shaking, and 3= deep sedation, not aroused by speaking or gentle shaking.
Time Frame
During 24 hours postoperatively
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults female undergoing elective breast surgery
American Society of Anesthesiologists (ASA) classification I-III
Body mass index (BMI) 18.5-35 kg/m2
Exclusion Criteria:
Implanted pacemaker
Cardiac arrythmia
Autonomic nervous system (ANS) disorder, e.g. epilepsy, stroke
Chronic opioid use
Chronic pain
On beta-blocker, calcium channel blocker, or other drugs to control arrythmia
Previous mastectomy
Pregnancy
On Nsaids
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sirirat Tribuddharat, MD, PhD
Organizational Affiliation
Faculty of Medicine, Khon Kaen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Srinagarind Hospital, Faculty of Medicine, Khon Kaen University
City
Khon Kaen
ZIP/Postal Code
40002
Country
Thailand
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
24322571
Citation
Boselli E, Bouvet L, Begou G, Dabouz R, Davidson J, Deloste JY, Rahali N, Zadam A, Allaouchiche B. Prediction of immediate postoperative pain using the analgesia/nociception index: a prospective observational study. Br J Anaesth. 2014 Apr;112(4):715-21. doi: 10.1093/bja/aet407. Epub 2013 Dec 8.
Results Reference
result
PubMed Identifier
28628575
Citation
Daccache G, Jeanne M, Fletcher D. The Analgesia Nociception Index: Tailoring Opioid Administration. Anesth Analg. 2017 Jul;125(1):15-17. doi: 10.1213/ANE.0000000000002145. No abstract available.
Results Reference
result
PubMed Identifier
28631050
Citation
Dundar N, Kus A, Gurkan Y, Toker K, Solak M. Analgesia nociception index (ani) monitoring in patients with thoracic paravertebral block: a randomized controlled study. J Clin Monit Comput. 2018 Jun;32(3):481-486. doi: 10.1007/s10877-017-0036-9. Epub 2017 Jun 19.
Results Reference
result
PubMed Identifier
33581721
Citation
Tribuddharat S, Sathitkarnmanee T, Sukhong P, Thananun M, Promkhote P, Nonlhaopol D. Comparative study of analgesia nociception index (ANI) vs. standard pharmacokinetic pattern for guiding intraoperative fentanyl administration among mastectomy patients. BMC Anesthesiol. 2021 Feb 13;21(1):50. doi: 10.1186/s12871-021-01272-2.
Results Reference
derived
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Intraoperative Fentanyl Consumption Guided by Analgesia Nociception Index
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