Study of Oral Uremic Toxin Absorbent and Probiotics to Retard the Progression of Chronic Kidney Disease

NARecruitingINTERVENTIONAL
Enrollment

180

Participants

Timeline

Start Date

May 1, 2020

Primary Completion Date

December 1, 2030

Study Completion Date

December 1, 2030

Conditions
CKD
Interventions
DIETARY_SUPPLEMENT

Active bamboo charcoal

During this 6 months' trial, eligible 120 patients with eGFR 15 \< eGFR \< 45 ml/min/1.73m2 and UACR \> 100 mg/g will be enrolled and randomized into 4 groups. The patients in group 1 will receive CharXenPlus 4g (with ABC 2g) thrice daily + CharXprob 0.8 g once daily in the initial 3 months. Group 2 will receive CharXenPlus 4g thrice daily in the initial 3 months, and CharXprob 0.8 g once daily in the last 3 months. Group 3 will receive CharXprob 0.8 g once daily in the initial 3 months, and CharXenPlus 4g thrice daily in the last 3 months. Group 4 will only receive CharXprob 0.8 g once daily in the last 3 months.

DIETARY_SUPPLEMENT

Probiotics

Probiotics

Trial Locations (1)

Unknown

RECRUITING

NTUH, Taipei

All Listed Sponsors
lead

National Taiwan University Hospital

OTHER