Last updated: April 4, 2024
Sponsor: Emory University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Scar Tissue
Cystic Fibrosis
Lung Disease
Treatment
Hi GI
Lo GI
Sugar Sweetened Beverages (SSB)
Clinical Study ID
NCT06350149
STUDY00004637
1R21DK128731-01A1
Ages 12-21 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- English speaking
- Diagnosis of CF based on the presence of two known CF causing mutations and/orpositive sweat test
- Pancreatic insufficiency
- Baseline dietary consumption of >10% total kcal from added sugars and self-reportedconsumption of >/= sugar-sweetened beverages per week
Exclusion
Exclusion Criteria:
- Current use or anticipated use of medication that is known to raise or lower bloodglucose in the past 4 weeks.
- Oral or IV glucocorticoid current or previous use in the past 4 weeks will prohibitenrollment in the study.
- Recent pulmonary exacerbation within 3 weeks of enrollment and/or an acute illnessrequiring a change in antibiotics will also exclude participants.
- BMI below the 5th percentile or greater than the 95th percentile for age and sex
- FEV1 <40% or awaiting a lung transplant;
- Prior lung or liver transplant or kidney or liver dysfunction.
- Use of CFTR modulators is not an exclusion criterion. Rather, for patients recentlystarted on CFTR modulators, we will wait to enroll in the study until on CFTRmodulator for at least 2 months.
- Diagnosis of CF liver disease.
- Uncontrolled exocrine pancreatic insufficiency/malabsorption
- Diagnosis of CFRD
- G-tube feeds (bolus and/or continuous)
- Current enrollment in another intervention study
- Changes in diet to lose or gain weight
- Gluten allergy or intolerance
- Current pregnancy or lactation or plans to become pregnant during study period
- History of drug or alcohol abuse
- Restrictive dietary patterns (e.g, vegan, ketogenic, intermittent fasting) for morethan one month within the last two months prior to screening.
- More than 5% body weight change within 2 months of screening visit or Day 1 of mixedmeal tolerance test
Study Design
Total Participants: 40
Treatment Group(s): 3
Primary Treatment: Hi GI
Phase:
Study Start date:
March 22, 2024
Estimated Completion Date:
September 30, 2025
Study Description
Connect with a study center
Center for Advanced Pediatrics: Emory Healthcare
Atlanta, Georgia 30329
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.