Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
Cystic Fibrosis
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Parallel, double blind, randomizedMasking: Triple (Participant, Care Provider, Investigator)Masking Description: The supplement only differ by colour on capsulae, no labellingPrimary Purpose: Treatment

Participation Requirements

Age
Between 5 years and 15 years
Gender
Both males and females

Description

Two group of matched children with CF were randomized to two type of oils given 20 g oil and 800 mg DHA daily for one year and anthropometry, pulmonary function, biochemistry, resting energy expenditure, lipid mediators, inflammatory and intestinal markers were studied at start and at 6 months and 1...

Two group of matched children with CF were randomized to two type of oils given 20 g oil and 800 mg DHA daily for one year and anthropometry, pulmonary function, biochemistry, resting energy expenditure, lipid mediators, inflammatory and intestinal markers were studied at start and at 6 months and 1 year. Dietary intake was controlled and life quality recording at start and end of study.

Tracking Information

NCT #
NCT04531410
Collaborators
European Society of Pediatric Gastroenterology, Hepatology and Nutrition
Investigators
Principal Investigator: Jaroslaw Walkowiak, MD,PhD University of Poznan, CF center, Poland Principal Investigator: Carla Colombo, MD,PhD University of Milan, CF center, Italy Principal Investigator: Olav Trond Storrösten, MD, PhD University of Oslo, CF center, Norway