Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06576700

Effect of Procyanidins in Leaky Gut Repairing in IBD

Led by University of Padova · Updated on 2024-09-19

25

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if the Grape Seed Extract Ecovitis, featuring low monomeric catechins content and a high concentration of oligo-polymeric procyanidins, could modulate the Gut Microbiota composition of Ulcerative Colitis patients during the remission phase. The main questions it aims to answer are: Does Ecovitis improve the microbiota composition in patients with Ulcerative colitis? Is the intestinal permeability affected? What about the variation in the quality of life? Participants will: Take 2 capsules/day of Ecovitis for eight weeks Visit the clinic two times for checkups, serum collection, and Questionaire.

CONDITIONS

Official Title

Effect of Procyanidins in Leaky Gut Repairing in IBD

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Ulcerative Colitis confirmed by clinical, endoscopic and histopathological evidence with disease in remission phase
  • Age between 18 and 75 years old
  • Ability to fully participate in all aspects of the clinical trial
Not Eligible

You will not qualify if you...

  • Active Ulcerative Colitis determined by clinical, endoscopic and histopathological evidence
  • Diagnosis of Crohn's Disease, indeterminate colitis, ischemic colitis, radiation colitis, diverticular disease associated with colitis, or microscopic colitis
  • Positive stool culture for active Clostridium difficile
  • Pregnant women
  • Antibiotic and/or probiotic treatment within 10 days prior to the first visit

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Edoardo Vincenzo Savarino

Padua, Padua, Italy, 35128

Actively Recruiting

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Research Team

E

Edoardo V. Savarino, MD; PhD

CONTACT

S

Sonia Facchin, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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