Actively Recruiting

Phase Not Applicable
Age: 0 - 18Years
All Genders
NCT05561738

Nicotinamide Riboside in Ulcerative Colitis

Led by University of Pittsburgh · Updated on 2026-01-20

40

Participants Needed

1

Research Sites

121 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

C

Crohn's and Colitis Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a randomized, double-blind pilot study of Nicotinamide Riboside (NR) in Pediatric-onset Ulcerative Colitis (UC).

CONDITIONS

Official Title

Nicotinamide Riboside in Ulcerative Colitis

Who Can Participate

Age: 0 - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pediatric patients 18 years old or younger
  • Diagnosis of mild to moderate ulcerative colitis confirmed by Pediatric Ulcerative Colitis Activity Index and endoscopic Mayo scoring at colonoscopy
  • Newly diagnosed (treatment naive) or patients with established disease
Not Eligible

You will not qualify if you...

  • Patients with acute severe ulcerative colitis
  • Concurrent gastrointestinal infections such as Clostridium difficile or Cytomegalovirus
  • Diagnosis of Crohn's disease
  • Indeterminate colitis or inflammatory bowel disease unclassified
  • Treatment with steroids or antibiotics in the past three months (patients on biologic medications with stable dose for at least three months may be enrolled)
  • Other chronic inflammatory or autoimmune disorders or prior malignancy
  • Pregnant women; women of childbearing age must use contraception at inclusion
  • Existing kidney or liver dysfunction
  • Platelet count less than 50,000 preventing endoscopy per standard care guidelines

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UPMC Children's Hospital of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15224

Actively Recruiting

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Research Team

M

Min Shi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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