Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Chronic Kidney Disease Stage 3B
  • Chronic Kidney Disease stage4
  • Diabetes Mellitus - Type 2
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: This is a multicentre randomized double-blinded controlled trial lasting 20 weeks with two study periods. The first 12 weeks will constitute a treatment period with BSE (BSE group) or placebo (Control group) depending on the randomization of the group allocation. After that, patients from both groups will be followed for another eigth weeks, called post-study observational period.Masking: Triple (Participant, Care Provider, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 90 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04858854
Collaborators
Lantmännen
Investigators
Principal Investigator: Peter x Stenvinkel, MD Karolinska Institutet Study Chair: Carla Avesani, PhD Karolinska Institutet Study Director: Marie Evans, MD Karolinska Institutet