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NCT07471542 · ClinicalTrials.gov registry record · NA

Copper Supplementation in Cirrhosis

A NA study of Cirrhosis and Infection, sponsored by University of Washington.

Recruiting
Registry status
NA
Development phase
30
Enrollment target
1
Study location

NCT07471542: Recruiting NA study of Cirrhosis and Infection, sponsored by University of Washington.

NCT07471542 is a NA study of Cirrhosis and Infection that is actively recruiting participants, run by University of Washington. The registered enrollment target is 30 participants, below the 90,408-participant average among 53 other Cirrhosis trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07471542, a NA study of Cirrhosis and Infection, is actively recruiting participants, sponsored by University of Washington.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
1
Study location

Study 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.

Primary Outcome

The primary endpoint is the mean change in plasma Cu concentration between baseline and each intervention period

Interventions

  • DIETARY_SUPPLEMENT Copper Gluconate

Study Locations (1)

Washington

  • University of Washington Medical Center - Seattle

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2026-03-15
Est. Completion 2028-12
Phase NA
University of Washington

1,048 total trials

What NCT07471542 shows while recruiting

NCT07471542 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 90,408-participant average among 53 other Cirrhosis trials with a reported enrollment target (100% lower).

The record links to 4 conditions, with Cirrhosis appearing as the primary indexed condition, and to 1 intervention - of which Copper Gluconate is the first listed.

NCT07471542 reports a single indexed study location in Washington.

Frequently Asked Questions

What is clinical trial NCT07471542 about?

NCT07471542 is a clinical study titled "Copper Supplementation in Cirrhosis". 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 p...

What is the current status of trial NCT07471542?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2026-03-15. Estimated completion is 2028-12.

What conditions does trial NCT07471542 study?

This clinical trial studies the following conditions: Cirrhosis, Infection, Fibrosis, Chronic Liver Disease.

What interventions are being tested in trial NCT07471542?

The interventions under investigation include: Copper Gluconate (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT07471542?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07471542 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cirrhosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07471542's enrollment target sits among peer trials

30 31st of 53 higher than 13 of 53 other Cirrhosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cirrhosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07471542, the US trial registry maintained by the National Library of Medicine. NCT07471542 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.