A Pilot Study to Determine Fructose Uptake by Primary Human Colorectal Tumors
Colorectal Tumors
About this trial
This is an interventional basic science trial for Colorectal Tumors focused on measuring Fructose, D-Xylose, Primary Human Colorectal Tumors
Eligibility Criteria
Inclusion Criteria:
- Subjects of 18 years of age or older, male, and female
- Subjects with a diagnosis of invasive non-hereditary colonic adenocarcinoma who will be undergoing standard of care (SOC) laparoscopic, robot-assisted, or open surgical resection
- The subject provides informed consent
Exclusion Criteria:
- Subjects with a history of uncontrolled diabetes mellitus (A1C >7.0) Type I and Type 2, will be excluded to avoid potential confounders associated with the consumption of a large bolus of sugar (e.g., hyperglycemia and hyperinsulinemia)
- Inflammatory Bowel Disease (Ulcerative Colitis or Crohn's Disease)
- Patients on steroid medications
- Patients with current infectious disease
- Subjects who do not speak English
Sites / Locations
- Weill Cornell MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Cohort 1: HFCS (fructose-fed)
Cohort 2: D-Xylose (xylose-fed)
Day Before Surgery between 09:00 pm and 10:00 pm Subjects will prepare the sugar solutions (Fructose-containing solution: 250 mL of water containing 41.25 g of D-Fructose and 33.75 g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Subjects will be reminded the day before the surgery to drink the solution.
Day Before Surgery between 09:00 pm and 10:00 pm Subjects will prepare the sugar solutions (Xylose-containing solution: 250 mL of water containing 41.25 g of D-Xylose and 33.75g of D-Glucose) by adding 250 ml water to the sugar powder provided by the study team and drink it between 09:00 pm and 10:00 pm. Subjects will be reminded the day before the surgery to drink the solution.