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Effects of Pomegranate Juice on Ulcerative Colitis

Recruiting

Effect of Pomegranate Juice on Gut Inflammation, Quality of Life and the Gut Microbiome in Patients With Ulcerative Colitis: A Pilot Study

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* • Adults ≥ 18 yo

  * Following a low-polyphenol and fiber diet (\< 3 servings of fruits/vegetables per day)
  * Mild-to-moderate UC at the time of screening (2 ≤ partial Mayo scores ≤ 5)
  * Supportive evidence of active inflammation (hsCRP \>1 mg/L, fecal calprotectin \>50 µg/g stool, or abnormal lower endoscopy) in individuals with biopsy-proven UC
  * Patients on 5-aminosalicylates must be on a stable dose for ≥ 4 weeks prior to screening
  * Patients on treatment with immunosuppressive therapy (e.g., azathioprine/6-mercaptopurine, methotrexate) must be on stable dose for 8 weeks prior to baseline visit
  * At the time of baseline visit, patients may be on no more than 20 mg/day of prednisone and 9 mg/day of budesonide MMX
  * Subjects must read and sign the Institutional Review Board-approved written informed consent prior to the initiation of any study specific procedures or enrollment. A subject will be excluded for any condition that might compromise the ability to give truly informed consent.

Exclusion Criteria:

* • Non-English speaker

  * Vegetarian/vegan
  * Known pomegranate allergy
  * Documented chronic disease besides UC, including diabetes, renal or liver diseases, metabolic syndrome, active cancer, MI or stroke, history of gastric bypass
  * Patients with CD, indeterminate/severe to fulminant colitis
  * History of colectomy or colonic dysplasia
  * Presence of ileal pouch or ostomy
  * Evidence of active bacterial or viral gastroenteritis as indicated by positive stool studies for ova \& parasites, Clostridium difficile, and stool culture
  * Recent hospitalizations (within 2 weeks of screening) for UC requiring IV steroids
  * Presence of the following labs indicative of severe colitis: a. Hemoglobin \< 8.0 g/dl b. Albumin \< 3.0 g/dl
  * Recent systemic antibiotics use (within 3 months of screening) or active use of anti-diarrheal medications
  * Taking supplements known to affect metabolism or gut microbiota composition (probiotics, fiber, etc.), unless willing to stop for the study duration
  * Use of Total Parenteral Nutrition (TPN)
  * Use of cyclosporine, tacrolimus, or thalidomide within 2 months prior to screening
  * Taking exogenous hormones (e.g., hormone replacement therapy)
  * Recent weight fluctuations (\>10% in the last 6 months)
  * Smoker or living with a smoker
  * Use of \>20 g of alcohol per day
  * Unable or unwilling to comply with the study protocol (including unwillingness to avoid watermelon and other lycopene-rich foods for the whole duration of the study)
  * Unable to provide consent

About the study

The purpose of this study is to determine whether consumption of 237 ml of pomegranate juice daily for 8 weeks will:

1. lower inflammation (in the gut as well as generally in the body) and improve your overall quality of life 2. affect the microbes living in the gut (gut microbiota)

What is being tested

Sponsor: University of California, Los Angeles · Participants: 30 · Started: Oct 15, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07115862

Locations in the U.S.

CaliforniaUCLA Center for Human Nutrition, Los Angeles
West Los Angeles VA Medical Center, Los Angeles (Not yet recruiting)

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.