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The Effect of AC-134 in Chronic Kidney Diseases

To Investigate the Protective Effect of AC 134 in Chronic Kidney Diseases.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06441435
Enrollment
100
Registered
2024-06-04
Start date
2024-06-05
Completion date
2025-06-30
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nephrology

Keywords

Chronic Kidney Diseases, Activated charcoal

Brief summary

The objective is to explore the effects of adding AC-134 on renal function, proteinuria, uremic toxins, and metabolism-related markers in chronic kidney disease.

Detailed description

Chronic kidney disease (CKD) management primarily focuses on addressing associated complications such as hypertension, diabetes mellitus, cardiovascular disease, and proteinuria. In addition to standard therapies, reducing the accumulation of toxins, particularly gut-derived uremic toxins like indoxyl sulfate (IS) and p-cresol sulfate (PCS), may help alleviate uremia symptoms. This study assesses the impact of oral AC-134 capsules containing activated charcoal adsorbent on CKD patients. The assessment will include evaluating changes in renal function, proteinuria, uremic toxins, and metabolism-related markers.

Interventions

DIETARY_SUPPLEMENTLow protein diet with AC-134

Low protein diet combined with AC-134 Dosage: 2 capsules,three times/day

OTHERStandard treatment

Low protein diet

Sponsors

Taichung Veterans General Hospital
Lead SponsorOTHER
All Clean Health Co., Ltd
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Aged 20-90 years. * Diagnosed with stage 3-5 chronic kidney disease, excluding dialysis patients. * Signed informed consent is required before enrollment.

Exclusion criteria

* Use of other brand-activated charcoal supplements during the study period. * Pregnant or lactating women. * Patients who have undergone kidney transplantation. * Obstructive nephropathy within the past month. * Acute kidney injury within the past three months. * Gastrointestinal bleeding or severe constipation within the past three months. * Patients with active malignancy within the past two years. * Severe cardiovascular diseases such as congestive heart failure New York class III-IV or cerebrovascular disease * Severe liver disease, such as liver cirrhosis with ascites. * Active infectious disease

Design outcomes

Primary

MeasureTime frameDescription
Estimated glomerular filtration rate (eGFR) measurementBaseline to 3 monthsThe eGFR level is a maker for kidney function
Blood Urea Nitrogen (BUN) levelsBaseline to 3 monthsBlood Urea Nitrogen
Uremic toxins assayBaseline to 3 monthsThe concentration of p-cresol sulfate level, indoxyl sulfates level, and acrolein in the subjects' blood samples

Secondary

MeasureTime frameDescription
Liver functionBaseline to 3 monthsThe concentration of ALT, AST, total bilirubin and direct bilirubin in the subjects' blood samples
Inflammation makersBaseline to 3 monthsThe concentration of inflammation makers in the subjects' blood samples
Nutrition statusBaseline to 3 monthsThe concentration of albumin, wbc and uric acid in the subjects' blood samples
Lipid analysisBaseline to 3 monthsThe concentration of total cholesterol , triglyceride , HDL-cholesterol and LDL-cholesterol in the subjects' blood samples
Sugar testBaseline to 3 monthsThe concentration of fasting sugar and HbA1C in the subjects' blood samples
The quality of lifeBaseline to 3 monthsIt will measure by the Kidney Disease Quality of Life (\[KDQOL\]-SF™) questionnaire
Anemia testBaseline to 3 monthsThe concentration of hemoglobin (Hb) in the subject's blood samples
Urine protein analysisBaseline to 3 monthsUrine specimen collection will be evaluated on the spot and 24-hour urine protein
24-hour Dietary recallBaseline to 3 monthsThere will be collected by food models or a photography atlas to estimate portion size
Gastrointestinal symptoms measuresBaseline to 3 monthsThere will be collected by questionnaires symptoms or chief complaints
Grip strength levelsBaseline to 3 monthsHand grip strength was measured by grip strength device
Blood gasBaseline to 3 monthsThe concentration of blood gas test in the subject's blood samples
Electrolytes AnalysisBaseline to 3 monthsThe concentration of electrolytes analysis in the subject's blood samples
Mitochondrial oxidative stressBaseline to 3 monthsThe concentration analysis in the subject's blood or urine samples, such as MDA

Countries

Taiwan

Contacts

PRINCIPAL_INVESTIGATORCheng-Hsu Chen, MDPHD

Division of Nephrology in Taichung Veterans General Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026