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Clinical Trials/NCT04311645
NCT04311645UnknownPhase 2

Role of Oral Activated Charcoal in Decreasing Blood Urea, Creatinine and Phosphorous in Chronic Kidney Disease

Assiut University0 sites90 target enrollmentStarted: August 1, 2020Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 2
Enrollment
90
Primary Endpoint
Mean of blood urea, creatinine and phosphorous in patients with CKD before and after oral activated charcoal

Study Overview

Brief Summary

The study aims to explore the ability of Oral activated charcoal to adsorb uremic toxins limiting the progression of chronic kidney disease and delaying the need for hemodialysis in patients with CKD stages III and IV.

To compare its effect with the effect of dry seeds as absorbents of uremic toxins

Detailed Description

In recent years, chronic kidney disease(CKD) has become a worldwide public health issue.

The main factors affecting the prognosis of patients with chronic kidney disease are its complications, including cardiovascular and cerebrovascular diseases, malnutrition, inflammation, atherosclerosis syndrome, and anemia.

The accumulation of uremic toxins, such as indoxyl sulfate and p-cresyl sulfate, is implicated in the progression of renal failure and cardiovascular disease.

For many patients, chronic kidney disease (CKD) is a progressive condition marked by deteriorating renal function ultimately leading to end-stage renal disease (ESRD) and many patients refuse to start chronic hemodialysis.

Therapeutic approaches that decrease the level of uremic toxins are a rational method for inhibiting this progression.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with CKD stages iii and iv
  • Patients with age more than 18 years old

Exclusion Criteria

  • Patients on regular hemodialysis
  • Patients with age less than 18 years old

Arms & Interventions

1st group

Other

Oral activated charcoal in a dose of 30 gm/day

Intervention: Activated charcoal (Drug)

2nd group

Other

Dry seeds in a dose of 1 gm/ day

Intervention: Dry seeds (Dietary Supplement)

Outcomes

Primary Outcomes

Mean of blood urea, creatinine and phosphorous in patients with CKD before and after oral activated charcoal

Time Frame: baseline

to asses the mean of blood urea, creatinine and phosphorous in CKD patient before and after administration of activated charcoal

Secondary Outcomes

  • comparison of dry seeds and activated charcoal in limitting progression of chronic kidney disease(baseline)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Farrag Sayed Mohamed

Resident Doctor, internal medicine department, principal investigator

Assiut University

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