Recruiting

Cu Supplementation

Sponsor:

University of Washington

Code:

NCT07471542

Conditions

Cirrhosis

Chronic Liver Disease

Fibrosis

Infection

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Copper Gluconate

Study Details

Brief summary:

End stage liver disease or cirrhosis is a major cause of mortality in the United States and the world. Other than targeting the underlying cause, such as alcohol cessation and antiviral therapy, very few medical treatments can change the natural history of cirrhosis. Malnutrition is one of the few potentially modifiable factors that have been associated with cirrhosis severity and poor prognosis. The transition metal copper (Cu) is an essential trace metal that must be acquired from diet. Its metabolism is primarily regulated by the liver in its role as a master regulator of nutrients. In 2019, the investigators reported that Cu deficiency defined by below normal serum or liver concentrations occurred in a wide range of liver disorders and was associated with a severe disease phenotype. Improvement in liver function was observed in 2 of the 3 patients who received Cu supplementation. In 2023, the investigators conducted a longitudinal cohort study utilizing clinical, serum and liver explant tissue data from 183 cirrhosis patients. The investigators showed that Cu deficiency was associated with 2-fold higher infection rate and a more than 3-fold increase in the risk of death compared to patients with normal Cu status. These preliminary findings and the well-established importance of Cu in human health prompted the investigators to design the current pilot randomized, placebo-controlled, crossover trial to determine the effect of Cu supplementation on Cu dependent biochemical changes, patient safety and patient reported outcomes in cirrhosis.

Conditions

Cirrhosis

Chronic Liver Disease

Fibrosis

Infection

Study ID

NCT07471542

Start date

Mar 15, 2026

Status verified date

Mar, 2026

Completion date

Dec, 2028

Anticipated

Primary completion date

Dec, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Adult patients age 18 or older with confirmed diagnosis of cirrhosis based on clinical history, exam, imaging, laboratory or histological criteria;
2. Cirrhosis patients whose serum or plasma Cu are below the normal range (80-155 ug/dL for women and 70-140 ug/dL for men);
3. Cirrhosis patients whose serum or plasma Cu are in the normal range but exhibit at least one clinical feature that has been associated with Cu deficiency. These include history of infections, unexplained anemia, severe leukopenia, iron overload, unexplained neurological symptoms such as ataxia or myelopathy, coagulopathy with spontaneous bleeding.

Patients must meet inclusion criteria 1 AND 2, or 1 AND 3 in order to be considered for the trial

Exclusion Criteria:

1. Patients with Wilson disease, cholestatic liver diseases including primary biliary cholangitis and primary sclerosing cholangitis, all of which are associated with Cu overload;
2. Patients with fulminant hepatic failure;
3. Renal failure with a creatinine clearance <25 ml/minute;
4. Hepatic encephalopathy more than grade 2 (Hepatic Encephalopathy in Chronic Liver Disease, 2014);
5. MELD score >25 to minimize subject dropout due to been too ill;
6. Serious non-liver related medical illnesses such as cardiopulmonary and renal diseases and non-liver malignancies;
7. Active alcohol use;
8. Pregnancy

Study Design

Enrollment

30 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Copper supplementation 1st arm

copper supplementation first, washout, then placebo

experimental: Placebo first arm

Placebo first, washout, then copper supplementation

Interventions

Copper Gluconate

Oral copper gluconate 4 mg daily

Primary outcome measure

  • Plasma copper (Cu) concentration [ Time Frame: From randomization to 1. end 6-week; 2. end of 9-week; 3. end of 15 week. First 6 week is intervention period 1 (either copper or placebo); followed by a 3-week washout period; followed by another 6-week intervention period (either placebo or copper). ]

Central Contacts and Locations

Central contacts

Locations

University of Washington Medical Center

Recruiting

Seattle, Washington, United States, 98195

Contacts

Shukriyah Samoun, BS

2065433220shukrs@uw.edu

Principal Investigator:

Lei Yu, MD

More Information

Sponsor

University of Washington

Last update posted

Mar 13, 2026

Last verified

Mar, 2026

Keywords

  • copper
  • cirrhosis
  • malnutrition

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Washington on 2026-03-13.