Quantification of Cannabinoids and Comparison to Post-Surgical Pain Medication Requirements and Surgical Outcomes
- Conditions
- Cannabis UsePost-Surgical PainCancerPost-Surgical Complication
- Registration Number
- NCT04988490
- Lead Sponsor
- University of Colorado, Denver
- Brief Summary
To determine how daily cannabis use affects surgical outcomes.
- Detailed Description
To determine if patients who are daily cannabis users that are undergoing inpatient abdominal surgery for the treatment of cancer are different from non-cannabis users regarding phytocannabinoid and endocannabinoid levels, pain scores, pain medication requirements, and surgical complications.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 80
- Patients > 18 years old
- Undergoing abdominal surgery for the treatment of cancer
- Report no cannabis use in the last year or chronic cannabis use (defined as at least weekly use for 3 months or more)
- patients with chronic pain, chronic pain syndrome on opioids
- female patients who are pregnant or lactating
- patients who report use of illicit substances
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative opioid consumption 30 days Postoperative opioid consumption among daily cannabis using and non-cannabis using patients undergoing abdominal surgery for cancer
Correlation of postoperative complications 30 days Correlation between 30-day post-operative complications, preoperative, and postoperative phytocannabinoid and endocannabinoid levels
Correlation of postoperative opioid consumption 30 days Correlation between serum phytocannabinoid and endocannabinoid levels, pain scores, and postoperative opioid consumption
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Colorado Hospital
🇺🇸Denver, Colorado, United States