The Impact of Perioperative Ketamine Infusion on Surgical Recovery
Primary Purpose
Opioid Use, Enhanced Recovery After Surgery, Anesthesia
Status
Enrolling by invitation
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ketamine
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Opioid Use focused on measuring ERAS, Enhanced Recovery After Surgery, Ketamine, Opioid, Learning Healthcare System
Eligibility Criteria
Inclusion Criteria:
- 18 years old or greater
- presenting at VUMC for abdominal surgery on the colorectal, ventral hernia or surgical oncology services on a weekday.
Exclusion Criteria:
- allergy or contraindication to ketamine
- unable or refuse to receive a regional nerve block
- patient refusal
- direct transfer from operating room to intensive care unit with endotracheal tube placed
Sites / Locations
- Vanderbilt University Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Ketamine
Saline
Arm Description
Participants in this arm will receive intraoperative ketamine bolus (0.5mg/kg) followed by continuous infusion 5 mcg/kg/min and also will receive postoperative ketamine infusion (2.5 mcg/kg/min, up to 100kg max) for 48 hours.
Participants in this arm will receive an equivalent volume of intraoperative saline bolus followed by continuous saline infusion and also will receive postoperative saline infusion for 48 hours.
Outcomes
Primary Outcome Measures
Length of Stay
The participants length of stay, from anesthesia beginning to discharge, measured in days
Secondary Outcome Measures
Total consumption of inpatient opioids
Inpatient opioid consumption measured in morphine milligram equivalents
Incidence of Surgical Outcomes - Gastrointestinal Complications
Incidence of ileus requiring gastric decompression as defined by orogastric or nasogastric tube placement in the postoperative period.
Incidence of Surgical Outcomes - Rapid Response
Rapid response as a binary outcome
Incidence of Surgical Outcomes - ICU Transfer
Transfer to ICU as a binary outcome
Incidence of Adverse Side Effects
Total incidence of side effects (hallucination, sedation, lightheadedness, patient request) as adverse reactions requiring early cessation.
Full Information
NCT ID
NCT04625283
First Posted
November 6, 2020
Last Updated
September 7, 2023
Sponsor
Vanderbilt University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT04625283
Brief Title
The Impact of Perioperative Ketamine Infusion on Surgical Recovery
Official Title
The Effect and Contribution of a Perioperative Ketamine Infusion in an Established Enhanced Recovery Pathway
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
April 12, 2021 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
April 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In order to effectively treat surgical pain with the least amount of opioids required, a multi-modal approach must include medications with different mechanisms of actions at alternative receptors. In light of the opioid epidemic, medical providers at Vanderbilt University Medical Center (VUMC) are strategically combining these medications in a bundled pain-regimen after surgery. These regimens have been shown to decrease opioid consumption, improve surgical outcomes, and reduce hospital stays, thus coining the term 'enhanced recovery pathway'. The combination of these medications has an indisputable synergistic effect. However, it is unknown how each medication contributes individually to the overall efficacy of the pathway. This study will examine the effects of ketamine, within the constructs of a multimodal pain regimen, on a) length of stay, b) opioid consumption, and c) surgical outcomes after major abdominal surgery.
Detailed Description
Opioids are powerful analgesic medications that can reduce pain through action at the mu receptor. Unfortunately, activation of the mu receptor also results in undesirable side effects, such as respiratory depression, sedation, bowel ileus, nausea, itching, and tolerance. Therefore, in order to effectively treat pain with the least amount of opioids required, a multi-modal approach must include medications with different mechanisms of actions at alternative receptors. Some examples of non-narcotic pain medications include acetaminophen (Tylenol), anti-inflammatories (NSAIDS), muscle relaxants, local anesthetics, gabapentinoids (Lyrica), and ketamine, to name a few. In light of the opioid epidemic, medical providers at Vanderbilt University Medical Center (VUMC) are strategically combining these medications in a bundled pain-regimen after surgery. These regimens have been shown to decrease opioid consumption, improve surgical outcomes, and reduce hospital stays, thus coining the term 'enhanced recovery pathway' or enhanced recovery after surgery (ERAS). The combination of these medications has an indisputable synergistic effect. However, it is unknown how each medication contributes individually to the overall efficacy of the pathway. Ultimately, the investigators aim to perform a series of randomized controlled trials in which we isolate each component of the pathway to investigate its effects on length of stay, total opioid consumption, and surgical outcomes. The investigators will begin with studying ketamine.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Use, Enhanced Recovery After Surgery, Anesthesia, Ketamine, Pain, Postoperative
Keywords
ERAS, Enhanced Recovery After Surgery, Ketamine, Opioid, Learning Healthcare System
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
This study will be performed as a pragmatic controlled clinical trial with parallel group assignment. Randomization will be in a cluster format.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1544 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ketamine
Arm Type
Experimental
Arm Description
Participants in this arm will receive intraoperative ketamine bolus (0.5mg/kg) followed by continuous infusion 5 mcg/kg/min and also will receive postoperative ketamine infusion (2.5 mcg/kg/min, up to 100kg max) for 48 hours.
Arm Title
Saline
Arm Type
Placebo Comparator
Arm Description
Participants in this arm will receive an equivalent volume of intraoperative saline bolus followed by continuous saline infusion and also will receive postoperative saline infusion for 48 hours.
Intervention Type
Drug
Intervention Name(s)
Ketamine
Other Intervention Name(s)
Ketalar
Intervention Description
Participants in the ketamine arm will receive intraoperative and postoperative ketamine.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Saline
Intervention Description
Participants in the placebo arm will receive intraoperative and postoperative saline.
Primary Outcome Measure Information:
Title
Length of Stay
Description
The participants length of stay, from anesthesia beginning to discharge, measured in days
Time Frame
From surgery start until discharge, typically 3-5 days
Secondary Outcome Measure Information:
Title
Total consumption of inpatient opioids
Description
Inpatient opioid consumption measured in morphine milligram equivalents
Time Frame
From hospital admission until discharge, typically 3-5 days
Title
Incidence of Surgical Outcomes - Gastrointestinal Complications
Description
Incidence of ileus requiring gastric decompression as defined by orogastric or nasogastric tube placement in the postoperative period.
Time Frame
From hospital admission until discharge, typically 3-5 days
Title
Incidence of Surgical Outcomes - Rapid Response
Description
Rapid response as a binary outcome
Time Frame
From hospital admission until discharge, typically 3-5 days
Title
Incidence of Surgical Outcomes - ICU Transfer
Description
Transfer to ICU as a binary outcome
Time Frame
From hospital admission until discharge, typically 3-5 days
Title
Incidence of Adverse Side Effects
Description
Total incidence of side effects (hallucination, sedation, lightheadedness, patient request) as adverse reactions requiring early cessation.
Time Frame
From hospital admission until discharge, typically 3-5 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years old or greater
presenting at VUMC for abdominal surgery on the colorectal, ventral hernia or surgical oncology services on a weekday.
Exclusion Criteria:
allergy or contraindication to ketamine
unable or refuse to receive a neuraxial or regional nerve block
patient refusal
direct transfer from operating room to intensive care unit with endotracheal tube placed
treating team elects to exclude the patient prior to study drug administration
abortion of planned surgical procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Britany L Raymond, MD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
The investigators do not plan to share individual participant data.
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The Impact of Perioperative Ketamine Infusion on Surgical Recovery
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