Opioid-free Anesthesia in Laparoscopic Cholecystectomies
Primary Purpose
Pain, Postoperative, Pain, Acute, Pain, Chronic
Status
Recruiting
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
ketamine-lidocaine-dexmedetomidine
fentanyl
Sponsored by
About this trial
This is an interventional prevention trial for Pain, Postoperative
Eligibility Criteria
Inclusion Criteria:
- adult patients
- American Society of Anesthesiologists (ASA) classification I-II
- elective laparoscopic cholecystectomy
Exclusion Criteria:
- body mass index (BMI) >35 kg/m2
- contraindications to local anesthetic administration or non-steroidal agents administration
- systematic use of analgesic agents preoperatively
- chronic pain syndromes preoperatively
- neurological or psychiatric disease on treatment
- pregnancy
- severe hepatic or renal disease
- history of cardiovascular diseases/ arrhythmias/ conduction abnormalities
- bradycardia(<55 beats/minute)
- drug or alcohol abuse
- language or communication barriers lack of informed consent
Sites / Locations
- Evangelismos General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
ketamine-lidocaine-dexmedetomidine (KLD) group
fentanyl (control) group
Arm Description
combination of ketamine-lidocaine-dexmedetomidine in one syringe
syringe of fentanyl
Outcomes
Primary Outcome Measures
pain score on arrival to Post-Anesthesia Care Unit (PACU)
pain score by the use of Numeric Rating Scale (NRS) on arrival to PACU, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
pain score at discharge from Post-Anesthesia Care Unit (PACU)
pain score by the use of Numeric Rating Scale (NRS) at discharge from PACU, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
pain score 3 hours postoperatively
pain score by the use of Numeric Rating Scale (NRS) 3 hours postoperatively, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
pain score 6 hours postoperatively
pain score by the use of Numeric Rating Scale (NRS) 6 hours postoperatively, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
pain score 24 hours postoperatively
pain score by the use of Numeric Rating Scale (NRS) 24 hours postoperatively, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
Secondary Outcome Measures
Post Anesthesia Care Unit (PACU) duration of stay
duration of patient stay at PACU
sedation on arrival to Post-Anesthesia Care Unit
sedation will be assessed with a 5-point sedation scale, where: 1, patient perfectly conscious; 2, patient feels a little drowsy; 3, patient seems to be sleeping but immediately reacts to verbal stimulation; 4, patient seems to be sleeping but slowly reacts to verbal stimulation and 5, patient seems to be sleeping and does not react to verbal stimulation but does react to a stimulus such as shaking or pain
sedation at discharge from Post-Anesthesia Care (PACU) Unit
sedation will be assessed with a 5-point sedation scale, where: 1, patient perfectly conscious; 2, patient feels a little drowsy; 3, patient seems to be sleeping but immediately reacts to verbal stimulation; 4, patient seems to be sleeping but slowly reacts to verbal stimulation and 5, patient seems to be sleeping and does not react to verbal stimulation but does react to a stimulus such as shaking or pain
sevoflurane consumption during general anesthesia
the sevoflurane vaporizer will be weighed before anesthetic induction and at the end of anesthesia and consequently sevoflurane consumption during anesthesia will be determined
time to first request for analgesia
the time for the first patient request for analgesia will be noted
morphine consumption in Post-Anesthesia Care Unit (PACU)
mg of morphine requested during patient PACU stay
tramadol consumption in the first 24 hours
patients will be followed for cumulative tramadol consumption for 24 hours postoperatively
sleep quality
subjective evaluation of sleep quality by patients, based on a sleep questionnaire (evaluation of sleep duration, number of nocturnal awakenings and marking of sleep quality
first mobilization after surgery
patients will be questioned regarding the time at which they mobilized after surgery
gastrointestinal recovery after surgery
patients will be questioned regarding the time they first felt enteral sounds and the time they had their first flatus after surgery
satisfaction from postoperative analgesia
satisfaction from postoperative analgesia on a six-point Likert scale with 1 marked as minimal satisfaction and 6 as maximal satisfaction
first fluid intake
patients will be questioned regarding the time they had their first fluid intake
first solid intake
patients will be questioned regarding the time they had their first solid intake
hospitalization time
duration of hospital stay after surgery in hours
fentanyl requirement during surgery
dose of required fentanyl intraoperatively to maintain systolic arterial blood pressure and heart rate within the 20% of baseline value
side effects intraoperatively
patients will be monitored for side-effects of the administered agents intraoperatively
side effects postoperatively
patients will be monitored for side-effects of the administered agents postoperatively
incidence of chronic pain 1 month after surgery
occurrence of chronic pain at the site of the operation 1 month after surgery, with the use of the Numeric Rating Scale (NRS), at rest and during movement
incidence of chronic pain 3 months after surgery
occurrence of chronic pain at the site of the operation 3 months after surgery, with the use of the Numeric Rating Scale (NRS), at rest and during movement
Full Information
NCT ID
NCT05089526
First Posted
October 10, 2021
Last Updated
February 23, 2023
Sponsor
Aretaieion University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05089526
Brief Title
Opioid-free Anesthesia in Laparoscopic Cholecystectomies
Official Title
Opioid-free Anesthesia With a Mixture of Dexmedetomidine-lidocaine-ketamine in Laparoscopic Cholecystectomies
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 11, 2021 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aretaieion University Hospital
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
The aim of this study will be to investigate the effect of an opioid-free anesthesia regimen with a mixture of dexmedetomidine-lidocaine-ketamine in the same syringe versus fentanyl analgesia in elective laparoscopic cholecystectomies
Detailed Description
Inadequately treated postoperative pain after laparoscopic cholecystectomy may untowardly affect early recovery and also lead to the development of chronic pain. Laparoscopic surgery is associated with diminished postoperative pain but this does not mean that patients subjected to laparoscopic operations are not in need for analgesia intra- and postoperatively. Pneumoperitoneum can lead to postoperative discomfort and occasionally intense postoperative shoulder pain. Opioid-based analgesia is associated with side-effects, such as respiratory depression, postoperative nausea and vomiting and occasional induction of tolerance and hyperalgesia.
Therefore, in recent years research has focused on the quest for non-opioid-based regimens for perioperative analgesia in the context of multimodal analgesic techniques. These techniques have been shown to possess significant advantages, such as allowing earlier mobilization after surgery, early resumption of enteral feeding and reduced hospital length of stay. In this context, the intraoperative intravenous injection of lidocaine has been reported to improve postoperative pain control, reduce opioid consumption and improve the quality of postoperative functional recovery after general anesthesia. Intraoperative infusions of ketamine (an N-methyl-D-aspartate receptor inhibitor) have also been correlated with reduced pain scores and a decrease in analgesic requirements postoperatively. Lastly, dexmedetomidine is a highly selective alfa-2 adreno-ceptor agonist that provides sedation, analgesia, and sympatholysis. Its perioperative intravenous administration has been associated with a reduction in postoperative pain intensity, analgesic consumption and nausea. There is insufficient data in literature investigating the effect of combinations of these agents intraoperatively. It would be of interest to demonstrate whether the administration of combinations can be used towards the achievement of a completely opioid-free anesthetic regimen. Additionally, it can be hypothesized that the combination of non-opioid drugs with different targets can lead to enhanced postoperative recovery, an improved opioid-sparing effect and a decrease in the development of chronic pain as compared to the administration of opioids. Therefore, the aim of this study will be to investigate the effect of a combination of intravenous infusions of lidocaine-ketamine-dexmedetomidine versus fentanyl on recovery profile and postoperative pain after elective laparoscopic cholecystectomy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative, Pain, Acute, Pain, Chronic, Cholecystectomy, Ketamine, Dexmedetomidine, Lidocaine, Central Nervous System Depressants, Analgesia, Analgesics, Analgesic Non-narcotic
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
ketamine-lidocaine-dexmedetomidine (KLD) group
Arm Type
Active Comparator
Arm Description
combination of ketamine-lidocaine-dexmedetomidine in one syringe
Arm Title
fentanyl (control) group
Arm Type
Active Comparator
Arm Description
syringe of fentanyl
Intervention Type
Drug
Intervention Name(s)
ketamine-lidocaine-dexmedetomidine
Other Intervention Name(s)
KLD group
Intervention Description
In the KLD group, patients will be administered 0,25 mcg/kg Dexmedetomidine in 100 mL of normal saline within 10 minutes. Followingly, they will receive 1mL/10 kg of the solution containing ketamine, lidocaine and dexmedetomidine at predefined concentrations. As maintenance, they will be receiving
1mL/10kg/h of the aforementioned solution.
Intervention Type
Drug
Intervention Name(s)
fentanyl
Other Intervention Name(s)
Control group
Intervention Description
In the fentanyl group, patients will be administered 2 mcg/kg fentanyl in 100 mL of normal saline within 10 minutes. Followingly, they will receive 1mL/10 kg of normal saline solution 0.9%. As maintenance, they will be receiving 1mL/10kg/h of normal saline solution 0.9%.
Primary Outcome Measure Information:
Title
pain score on arrival to Post-Anesthesia Care Unit (PACU)
Description
pain score by the use of Numeric Rating Scale (NRS) on arrival to PACU, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
Time Frame
immediately postoperatively
Title
pain score at discharge from Post-Anesthesia Care Unit (PACU)
Description
pain score by the use of Numeric Rating Scale (NRS) at discharge from PACU, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
Time Frame
at discharge from Post Anesthesia Care Unit (PACU), approximately 1 hour postoperatively
Title
pain score 3 hours postoperatively
Description
pain score by the use of Numeric Rating Scale (NRS) 3 hours postoperatively, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
Time Frame
3 hours postoperatively
Title
pain score 6 hours postoperatively
Description
pain score by the use of Numeric Rating Scale (NRS) 6 hours postoperatively, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
Time Frame
6 hours postoperatively
Title
pain score 24 hours postoperatively
Description
pain score by the use of Numeric Rating Scale (NRS) 24 hours postoperatively, ranging from 0 to 10, where 0 means "no pain" and 10 means "worst pain imaginable"
Time Frame
24 hours postoperatively
Secondary Outcome Measure Information:
Title
Post Anesthesia Care Unit (PACU) duration of stay
Description
duration of patient stay at PACU
Time Frame
immediately postoperatively
Title
sedation on arrival to Post-Anesthesia Care Unit
Description
sedation will be assessed with a 5-point sedation scale, where: 1, patient perfectly conscious; 2, patient feels a little drowsy; 3, patient seems to be sleeping but immediately reacts to verbal stimulation; 4, patient seems to be sleeping but slowly reacts to verbal stimulation and 5, patient seems to be sleeping and does not react to verbal stimulation but does react to a stimulus such as shaking or pain
Time Frame
immediately postoperatively
Title
sedation at discharge from Post-Anesthesia Care (PACU) Unit
Description
sedation will be assessed with a 5-point sedation scale, where: 1, patient perfectly conscious; 2, patient feels a little drowsy; 3, patient seems to be sleeping but immediately reacts to verbal stimulation; 4, patient seems to be sleeping but slowly reacts to verbal stimulation and 5, patient seems to be sleeping and does not react to verbal stimulation but does react to a stimulus such as shaking or pain
Time Frame
at discharge from Post Anesthesia Care Unit (PACU), approximately 1 hour postoperatively
Title
sevoflurane consumption during general anesthesia
Description
the sevoflurane vaporizer will be weighed before anesthetic induction and at the end of anesthesia and consequently sevoflurane consumption during anesthesia will be determined
Time Frame
change of sevoflurane vaporizer weight from before induction to end of anesthesia, an average period of 1-2 hours
Title
time to first request for analgesia
Description
the time for the first patient request for analgesia will be noted
Time Frame
during stay in Post-Anesthesia Care Unit (PACU), approximately 1 hour postoperatively
Title
morphine consumption in Post-Anesthesia Care Unit (PACU)
Description
mg of morphine requested during patient PACU stay
Time Frame
immediately postoperatively
Title
tramadol consumption in the first 24 hours
Description
patients will be followed for cumulative tramadol consumption for 24 hours postoperatively
Time Frame
24 hours postoperatively
Title
sleep quality
Description
subjective evaluation of sleep quality by patients, based on a sleep questionnaire (evaluation of sleep duration, number of nocturnal awakenings and marking of sleep quality
Time Frame
24 hours postoperatively
Title
first mobilization after surgery
Description
patients will be questioned regarding the time at which they mobilized after surgery
Time Frame
24 hours postoperatively
Title
gastrointestinal recovery after surgery
Description
patients will be questioned regarding the time they first felt enteral sounds and the time they had their first flatus after surgery
Time Frame
24 hours postoperatively
Title
satisfaction from postoperative analgesia
Description
satisfaction from postoperative analgesia on a six-point Likert scale with 1 marked as minimal satisfaction and 6 as maximal satisfaction
Time Frame
24 hours postoperatively
Title
first fluid intake
Description
patients will be questioned regarding the time they had their first fluid intake
Time Frame
24 hours postoperatively
Title
first solid intake
Description
patients will be questioned regarding the time they had their first solid intake
Time Frame
24 hours postoperatively
Title
hospitalization time
Description
duration of hospital stay after surgery in hours
Time Frame
96 hours postoperatively
Title
fentanyl requirement during surgery
Description
dose of required fentanyl intraoperatively to maintain systolic arterial blood pressure and heart rate within the 20% of baseline value
Time Frame
intraoperatively
Title
side effects intraoperatively
Description
patients will be monitored for side-effects of the administered agents intraoperatively
Time Frame
intraoperatively
Title
side effects postoperatively
Description
patients will be monitored for side-effects of the administered agents postoperatively
Time Frame
48 hours postoperatively
Title
incidence of chronic pain 1 month after surgery
Description
occurrence of chronic pain at the site of the operation 1 month after surgery, with the use of the Numeric Rating Scale (NRS), at rest and during movement
Time Frame
1 month after surgery
Title
incidence of chronic pain 3 months after surgery
Description
occurrence of chronic pain at the site of the operation 3 months after surgery, with the use of the Numeric Rating Scale (NRS), at rest and during movement
Time Frame
3 months after surgery
Other Pre-specified Outcome Measures:
Title
time to emergence
Description
time from sevoflurane discontinuation to first patient response (eye opening)
Time Frame
up to 2-3 hours after start of surgery
Title
time to extubation
Description
time from sevoflurane discontinuation to tracheal extubation
Time Frame
up to 2-3 hours after start of surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
adult patients
American Society of Anesthesiologists (ASA) classification I-II
elective laparoscopic cholecystectomy
Exclusion Criteria:
body mass index (BMI) >35 kg/m2
contraindications to local anesthetic administration or non-steroidal agents administration
systematic use of analgesic agents preoperatively
chronic pain syndromes preoperatively
neurological or psychiatric disease on treatment
pregnancy
severe hepatic or renal disease
history of cardiovascular diseases/ arrhythmias/ conduction abnormalities
bradycardia(<55 beats/minute)
drug or alcohol abuse
language or communication barriers lack of informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kassiani Theodoraki, PhD, DESA
Phone
+306974634162
Email
ktheodoraki@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Kyriakos Kyriazos
Email
kyriakos.kyriazos5@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kassiani Theodoraki
Organizational Affiliation
Aretaieion University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Evangelismos General Hospital
City
Athens
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kyriakos Kyriazos, MD
Email
kyriakos.kyriazos5@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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29739537
Citation
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Opioid-free Anesthesia in Laparoscopic Cholecystectomies
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