Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Absorption; Disorder
  • Absorption; Disorder, Carbohydrate
  • Absorption; Disorder, Fat
  • Absorption; Disorder, Protein
  • Crohn Disease
  • Malnutrition
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Multicentric, parallel, randomized, double blind and controlled clinical-nutritional study of 6 months of intervention and 3 study groups of treatment: Experimental group (peptidic diet with a mix of probiotics); Experimental group with placebo (peptidic diet with a placebo); and Control group (cont...

Multicentric, parallel, randomized, double blind and controlled clinical-nutritional study of 6 months of intervention and 3 study groups of treatment: Experimental group (peptidic diet with a mix of probiotics); Experimental group with placebo (peptidic diet with a placebo); and Control group (control with a polymeric nutritional oral supplement with a placebo) to evaluate the effect on the nutritional status, inflammatory markers and the intestinal absorption

Tracking Information

NCT #
NCT04305535
Collaborators
  • Adventia Pharma, S.L.
  • Biopolis S.L.
Investigators
Principal Investigator: Miguel Aganzo-Yeves, RD Hospital Universitario Fundación Jiménez Díaz Study Director: Clotilde Vázquez-Martínez, MD Hospital Universitario Fundación Jiménez Díaz