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Quantification of Cannabinoids and Comparison to Post-Surgical Pain Medication Requirements and Surgical Outcomes

Recruiting
Conditions
Cannabis Use
Post-Surgical Pain
Cancer
Post-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
Inclusion Criteria
  • 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)
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Exclusion Criteria
  • patients with chronic pain, chronic pain syndrome on opioids
  • female patients who are pregnant or lactating
  • patients who report use of illicit substances
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative opioid consumption30 days

Postoperative opioid consumption among daily cannabis using and non-cannabis using patients undergoing abdominal surgery for cancer

Correlation of postoperative complications30 days

Correlation between 30-day post-operative complications, preoperative, and postoperative phytocannabinoid and endocannabinoid levels

Correlation of postoperative opioid consumption30 days

Correlation between serum phytocannabinoid and endocannabinoid levels, pain scores, and postoperative opioid consumption

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Colorado Hospital

🇺🇸

Denver, Colorado, United States

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