Effects of Pomegranate Juice on Ulcerative Colitis
Recruiting
N/AInterventional Study
Ulcerative Colitis (Disorder)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
30 (estimated)
Sponsor
University of California, Los Angeles · Other
Who this trial is looking for
This trial is looking for adults with mild to moderate ulcerative colitis. Participants will drink 237 ml of pomegranate juice daily for 8 weeks to see if it helps reduce inflammation and improve gut health.
Are You a Good Fit for This Trial?
Rules you outChronic kidney diseaseChronic liver diseaseActive cancerRecent systemic antibiotics
You may be able to join if
I am at least 18 years old.
I have mild to moderate ulcerative colitis.
I follow a low-polyphenol and fiber diet.
I have signs of active inflammation.
I have been stable on my medications for UC for a certain amount of time.
I can give informed consent.
You may not be able to join if
I am a non-English speaker.
I have a known allergy to pomegranate.
I have a chronic disease besides ulcerative colitis.
I have had recent hospitalization for ulcerative colitis.
I am a smoker or live with a smoker.
I cannot avoid certain foods during the study.
I have had recent weight fluctuations.
I am unable to provide consent.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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)
Trial Locations
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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 µ…
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
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