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L-carnitine Corrects Ammonia Metabolism in Hepatectomized Patients

L-carnitine Corrects Ammonia Metabolism in Hepatectomized Patients

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03021876
Enrollment
80
Registered
2017-01-16
Start date
2016-04-30
Completion date
2018-04-30
Last updated
2017-01-16

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

Conditions

Ammonia Metabolism

Brief summary

L-carnitine is synthesized from lysine and methionine. Postmortem concentrations of carnitine in liver, muscle, heart, kidney, and brain averaged only one-fourth to one-third those in corresponding tissues of eight normally nourished non-hepatic patients who died after an acute illness of a 1-3-day duration. In the recent years, it has been reported that sirtuin 3 (SIRT3) is protective against acute kidney injury (AKI) and suggest that enhancing SIRT3 to improve mitochondrial dynamics has potential as a strategy for improving outcomes of renal injury. In the current study, it is the first clinical interventional research whether L-carnitine corrects ammonia metabolism associated with liver injury in hepatectomized patients.

Interventions

DRUGL-carnitine

treatment with oral L-carnitine, 1500 mg/body per day

baseliner

Sponsors

Kochi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients were those surgically treated for hepato-biliary diseases

Exclusion criteria

* Patient

Design outcomes

Primary

MeasureTime frameDescription
postoperative ammonia levels3 points; preoperative baseline, postoperative day 1, and day3change from preoperative baseline at postoperative day 1 and day3

Secondary

MeasureTime frameDescription
length of hospitalization after liver resectionup to 24 weekspostoperative days

Countries

Japan

Contacts

Primary ContactTakehiro Okabayashi, MD
tokabaya@gmail.com+81 88-837-3000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026