Anesthesia Clinical Trial
Official title:
The Effect and Contribution of a Perioperative Ketamine Infusion in an Established Enhanced Recovery Pathway
Verified date | February 2024 |
Source | Vanderbilt University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 1544 |
Est. completion date | February 1, 2024 |
Est. primary completion date | January 26, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt University Medical Center | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University Medical Center |
United States,
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Length of Stay | The participants length of stay, from anesthesia beginning to discharge, measured in days | From surgery start until discharge, typically 3-5 days | |
Secondary | Total consumption of inpatient opioids | Inpatient opioid consumption measured in morphine milligram equivalents | From hospital admission until discharge, typically 3-5 days | |
Secondary | Incidence of Surgical Outcomes - Gastrointestinal Complications | Incidence of ileus requiring gastric decompression as defined by orogastric or nasogastric tube placement in the postoperative period. | From hospital admission until discharge, typically 3-5 days | |
Secondary | Incidence of Surgical Outcomes - Rapid Response | Rapid response as a binary outcome | From hospital admission until discharge, typically 3-5 days | |
Secondary | Incidence of Surgical Outcomes - ICU Transfer | Transfer to ICU as a binary outcome | From hospital admission until discharge, typically 3-5 days | |
Secondary | Incidence of Adverse Side Effects | Total incidence of side effects (hallucination, sedation, lightheadedness, patient request) as adverse reactions requiring early cessation. | From hospital admission until discharge, typically 3-5 days |
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