RECRUITING

Baclofen for Children With Rumination Syndrome

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

The goal of this clinical trial is to learn about baclofen in pediatric patients with rumination syndrome. The main question it aims to answer is whether baclofen is effective in treating children with rumination syndrome. Participants will be asked to take baclofen or placebo for 4 weeks and fill out surveys regarding symptoms.

Official Title

A Randomized Controlled Pilot Trial of Baclofen for Children With Rumination Syndrome

Quick Facts

Study Start:2023-01-31
Study Completion:2024-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05975684

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:4 Years to 18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Children 4-18 years of age who meets Rome IV diagnostic criteria for rumination syndrome and are see at NCH GI clinic
  1. * Patients who have contraindications to baclofen due to medical history and/or current medications
  2. * Patients who are non- English speaking
  3. * Patients who are pregnant

Contacts and Locations

Study Contact

Peter Lu, MD, MS
CONTACT
6147223450
peter.lu@nationwidechildrens.org
Janice Khoo, MD
CONTACT
6147223450
janice.khoo@nationwidechildrens.org

Study Locations (Sites)

Nationwide Children's Hospital
Columbus, Ohio, 73205
United States

Collaborators and Investigators

Sponsor: Nationwide Children's Hospital

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 Date2023-01-31
Study Completion Date2024-07

Study Record Updates

Study Start Date2023-01-31
Study Completion Date2024-07

Terms related to this study

Additional Relevant MeSH Terms

  • Rumination Syndrome