RECRUITING

Clinical, Imaging, and Endoscopic Outcomes of Children Newly Diagnosed With Crohn's Disease

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Crohn's disease (CD) is a condition that causes inflammation (swelling, redness) of the lining and wall of the small intestine, large intestine, or both. CD may be associated with abdominal cramps/pain, diarrhea, blood in the stool, weight loss, or delayed growth in children. While the exact cause of CD is not certain it is thought that the immune system located in the intestine reacts abnormally to the large number of bacteria contained there. The investigators think that diet, exposure to antibiotics early in life, and having a family history of CD puts people at increased risk for developing CD. In order to decrease the inflammation doctors use what is called biologic therapy with anti-TNF molecules that can be given through an intravenous or shots. TNF is a chemical made by white blood cells that is involved in inflammation. When this type of treatment is given early after diagnosis it is more effective than when it is given later. The investigators have learned that it is important to give the optimum (ideal) amount of this medicine guided by certain blood tests. The investigators also know that not everyone responds to this therapy but do not understand the reasons for this variability between people. The CAMEO study has been started to help understand what factors are important in determining whether a child with CD completely heals the inflammation after anti-TNF therapy. The investigators will do that by measuring certain markers of inflammation in the blood and stool and by looking at a person's genes (DNA) and how inflammation is controlled in the intestine. These inflammation tests will be done before, during, and after one year of anti-TNF therapy. The investigators will determine how much healing has taken place by comparing the results of the colonoscopy and a special type of MRI that are both done before anti-TNF and then again one year later. The goal in treating CD is to heal both the lining and the wall of the intestine. Children ages 6-17 years who are thought to have CD and are about to undergo their diagnostic colonoscopy are eligible to be enrolled. If they are found to indeed have CD and start an anti-TNF medicine within 6 months they can continue in the study. There are no increased risks of participating in this study beyond those normally associated with having CD and its treatment. By better understanding why the bowel does or does not heal, doctors will be better able to provide personalized care.

Official Title

Clinical, Imaging, and Endoscopic Outcomes of Children Newly Diagnosed With Crohn's Disease

Quick Facts

Study Start:2023-06-10
Study Completion:2029-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05781152

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:6 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Dena E Hopkins, MPH, CCRP
CONTACT
860-545-8125
CAMEO_CCC@connecticutchildrens.org
Jeffrey S Hyams, MD
CONTACT
860-545-9560
jhyams@connecticutchildrens.org

Principal Investigator

Jeffrey S Hyams, MD
PRINCIPAL_INVESTIGATOR
Connecticut Children's Medical Center
Subra Kugathasan, MD
PRINCIPAL_INVESTIGATOR
Emory University
Lee Denson, MD
PRINCIPAL_INVESTIGATOR
Children's Hospital Medical Center, Cincinnati

Study Locations (Sites)

Phoenix Children's Hospital
Phoenix, Arizona, 85016
United States
Cedars-Sinai
Los Angeles, California, 90048
United States
Rady Children's Hospital - San Diego and University of California, San Diego
San Diego, California, 92123
United States
UCSF Benioff Children's Hospitals
San Francisco, California, 94158
United States
Connecticut Children's Medical Center
Hartford, Connecticut, 06106
United States
Emory University
Atlanta, Georgia, 30328
United States
Riley Hospital for Children at Indiana University Health
Indianapolis, Indiana, 46202
United States
The Johns Hopkins Children's Medical Center
Baltimore, Maryland, 21287
United States
Boston Children's Hospital
Boston, Massachusetts, 02115
United States
University of Michigan
Ann Arbor, Michigan, 48109
United States
Goryeb Children's Hospital/Morristown Medical Center/Atlantic Children's Health
Morristown, New Jersey, 07960
United States
Cohen Children's Medical Center of NY
Lake Success, New York, 11042
United States
Columbia University Medical Center
New York, New York, 10032
United States
Levine Children's
Charlotte, North Carolina, 28203
United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229
United States
UH/Rainbow Babies and Children's Hospital
Cleveland, Ohio, 44106
United States
Nationwide Children's Hospital
Columbus, Ohio, 43205
United States
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, 19146
United States
UPMC Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania, 15224
United States
Rhode Island Hospital
Providence, Rhode Island, 02903
United States
Seattle Children's Hospital
Seattle, Washington, 98105
United States
Medical College of Wisconsin
Milwaukee, Wisconsin, 53226
United States

Collaborators and Investigators

Sponsor: Connecticut Children's Medical Center

  • Jeffrey S Hyams, MD, PRINCIPAL_INVESTIGATOR, Connecticut Children's Medical Center
  • Subra Kugathasan, MD, PRINCIPAL_INVESTIGATOR, Emory University
  • Lee Denson, MD, PRINCIPAL_INVESTIGATOR, Children's Hospital Medical Center, Cincinnati

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-10
Study Completion Date2029-07-01

Study Record Updates

Study Start Date2023-06-10
Study Completion Date2029-07-01

Terms related to this study

Keywords Provided by Researchers

  • crohn disease
  • children
  • pediatric
  • anti-TNF therapy
  • therapeutic drug monitoring
  • intestinal microbiome
  • inflammatory bowel disease
  • gene expression
  • genomic DNA

Additional Relevant MeSH Terms

  • Crohn Disease