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Repletion of Ergothioneine in Patients With Kidney Failure

Stanford University logo

Stanford University

Status

Enrolling

Conditions

Esrd

Treatments

Other: Placebo
Dietary Supplement: Ergothioneine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Dialysis removes potentially harmful chemicals from the blood but can also remove potentially valuable chemicals. One potentially valuable chemical called ergothioneine, which comes from the diet, is low in the blood of people receiving dialysis. For this research study, the investigators hope to learn how well a daily ergothioneine supplement will replenish the levels in the blood of people with kidney failure.

Enrollment

28 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • kidney failure receiving hemodialysis or peritoneal dialysis

Exclusion criteria

  • blood transfusion within 90 days
  • taking supplements which contain ergothioneine

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

28 participants in 2 patient groups, including a placebo group

Ergothioneine
Experimental group
Description:
Ergothioneine (range 5 mg to 25 mg) oral daily for up to 12 weeks
Treatment:
Dietary Supplement: Ergothioneine
Placebo
Placebo Comparator group
Description:
Matching placebo oral daily for up to 12 weeks
Treatment:
Other: Placebo

Trial contacts and locations

1

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Central trial contact

Tammy Sirich, MD

Data sourced from clinicaltrials.gov

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