Nutrition Supplement for Cystic Fibrosis

Part of paid clinical trials in Columbus, Ohio.

Sponsor
Ohio State University
Study ID
NCT07163078
Status
Not Yet Recruiting

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Conditions

  • Cystic Fibrosis (CF)

Eligibility Criteria

Sex
ALL
Age
18 Years - 50 Years
Healthy Volunteers
Not accepted

Interventions

  • Common form supplementation — DIETARY_SUPPLEMENT
    The intervention product would represent part of a typical supplement given to people including those with CF
  • Uncommon nutrient supplementation — DIETARY_SUPPLEMENT
    The intervention product would represent part of a possible new supplement given to people including those with CF

Study Details

The goal of this study is to learn if one nutrition supplement formula works better than a different formula in adults with cystic fibrosis. The main question being addressed is: Will certain atypical versions of certain nutrients outperform typical versions of these nutrients? This will be determined by examining blood measures of nutrient levels and/or indications of nutrient function indicators pre- and post-intervention. Participants will take the supplements for 6 weeks with a blood draw before and after that time.

Key Dates

Start date
Jun 30, 2026
Status verified
May 2026
Primary completion
Dec 31, 2026
Completion
Jan 31, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Active Comparator: Conventional nutrient forms
    People are given a supplement with nutrient forms typically used in supplements
  • Experimental: Non-common nutrient forms
    People are given a supplement with nutrient forms that are not the most commonly used forms in supplements

Primary Outcome Measure

Nutrient status assessor 1 [ Time Frame: From pre-supplementation to 6 weeks later ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Nationwide Children's Hospital-Ohio State UniversityColumbusOhio43016-

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