A Uremic Toxin Absorbent (AST-120) to Treat Hospital Acquired Acute Kidney Injury

NCT02687841 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 206

Last updated 2016-02-22

No results posted yet for this study

Summary

Hospital acquired acute kidney injury is an important negative outcome predictor for hospitalized patients. Uremic toxins accumulated after a given renal insult. Some of these uremic toxins are protein bound and may accumulated after renal impairment, owing to both impaired filtration, and inflammation. Recent animal studies have reported that accumulation of uremic toxins, namely indoxyl sulfate and p-cresol, would down regulate endothelial progenitor cells and in turn affect renal recovery. Elimination of these protein bound uremic toxins with an activated charcoal would help restore endothelial function. We will conduct a double blinded randomized placebo controlled trial, which aims to determine that if oral activated charcoal will retard progression of AKI. Also, a panel of markers for endothelial function will also be determined.

Conditions

Interventions

DRUG

AST-120and pentoxyphylline (PTX)

AST-120 2g 4 times a day for 5 days then AST-120 2g 3 times a day for 5 days pentoxyphylline 400mg QD PO x 10 days.

DRUG

pentoxyphylline (PTX)

pentoxyphylline 400mg QD PO x 10 days.

Sponsors & Collaborators

  • National Taiwan University Hospital, Yun-Lin Branch

    collaborator OTHER
  • National Taiwan University Hospital Hsin-Chu Branch

    collaborator OTHER
  • China Medical University Hospital

    collaborator OTHER
  • Taoyuan General Hospital

    collaborator OTHER_GOV
  • Taipei Medical University Hospital

    collaborator OTHER
  • Chang Gung Memorial Hospital

    collaborator OTHER
  • National Taiwan University Hospital

    lead OTHER

Principal Investigators

  • YU-SHENG WU · National Taiwan University Hospital

  • Tao-Min Huang · National Taiwan University Hospital, Yun-Lin Branch

  • Wei-Shun Yang · National Taiwan University Hospital Hsin-Chu Branch

  • JUI-HSIANG LIN · Taoyuan General Hospital

  • Ya-Fei Yang · China Medical University Hospital

  • Chan-Yu Lin · Chang Gung Memorial Hospital

  • Heng-Chih Pan · Chang Gung Memorial Hospital

  • Chih-Chin Kao · Taipei Medical University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2017-12-31
Completion
2017-12-31

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02687841 on ClinicalTrials.gov