L-citrulline to Improve Adverse Outcomes in Admitted Children (EChiLiBRiST, Clinical Trial 2, Inpatients)

Official title

A Randomised, Double-blind, Placebo-controlled Trial of L-Citrulline Oral Supplementation to Improve Short and Long-term Outcomes of Admitted Febrile Paediatric Patients With Biomarker-determined High-risk of Adverse Outcomes

Overview

In low and middle-income countries, children admitted to hospital are not similarly ill, and do not all have a comparable prognosis. In fact, understanding at first encounter their risk of developing adverse outcomes (including mortality) could allow a more focused management and the tailoring of specific interventions to decrease in hospital mortality, and post discharge adverse longer-term outcomes. This clinical trial, part of the EChiLiBRiST larger project ("Development and validation of a quantitative point-of-care test for the measurement of severity biomarkers to improve risk stratification of fever syndromes and enhance child survival") has the two-fold objective of: 1. Assessing whether a POINT-OF-CARE rapid triaging test (PoC RTT) based on the quantitative measurement at the bedside of the "prognostic" biomarker sTREM-1 (soluble-triggering receptor expressed on myeloid cells 1) can reliably identify those admitted children with a higher risk of adverse outcomes; and 2. Assessing whether the therapeutic intervention (the L-arginine precursor, L-Citrulline, key in the nitric oxide biosynthesis), administered orally for 28 days to those children aged 1-\<60 months identified as "moderate-to-high risk" by the prognostic biomarker can improve outcomes as compared to those receiving an indistinguishable placebo. This second objective will be assessed in a prospective multi-country, multi-site, individually randomised, two-arm, placebo-controlled, double blind clinical trial involving \~888 children 1-\<60m of age admitted to hospital and determined to be at high risk of adverse outcomes by their baseline sTREM-1 levels. The trial will compare the efficacy of a twice-daily dose of L-citrulline syrup vs placebo (200-300mg/kg/day depending on weight-band; for 28 days) in reducing adverse outcomes in children with severe disease. The trial will be running independently but in parallel in two high-mortality settings in Mozambique and in Ethiopia.

Detailed description

Children admitted to hospital and meeting the study eligibility criteria who are 0-\<60 months of age will be eligible for study inclusion, and for initial biomarker screening using the study-designed rapid triaging PoC test, based on the measurement of sTREM-1. Study participants aged 1m-\<5 years of age with sTREM-1 values classified as moderate (i.e., "yellow") or high-risk (i.e., "red") in the traffic light risk-stratification system will be randomly allocated (1:1) to receive L-Cit intervention or placebo. All study participants will be followed for 6 months, with study visits at the study hospitals or at home or via phone communication after discharge at day 3, day 5, day 7, day 28, and month 6. The study primary outcome will be "adverse disease outcome", defined as a composite of mortality, incident neurological sequelae, major adverse kidney event at discharge, need for organ support, clinical shock, coma, severe respiratory distress or need for readmission within 28 days after recruitment.

Interventions

• Dietary supplement L-citrulline
  1 or 2 sachets every 12 hours (200-300mg/kg/day depending on weight-band) for 28 days
• Dietary supplement Placebo
  1 or 2 sachets every 12 hours (depending on weight-band) for 28 days

Primary outcome measures

• Adverse disease outcome [Time frame: Up to day 28]

Secondary outcome measures (12)

• Mortality [Time frame: Up to day 28]
• Incident neurological sequelae [Time frame: Up to day 28]
• Major adverse kidney event [Time frame: Up to day 28]
• Need for organ support [Time frame: Up to day 28]
• Clinical shock [Time frame: Up to day 28]
• Severe respiratory distress [Time frame: Up to day 28]
• Coma [Time frame: Up to day 28]
• Need for readmission [Time frame: Up to day 28]
• Median duration of antibiotic treatment [Time frame: Up to day 28]
• Oxygen requirement [Time frame: Up to day 28]
• Radiological pneumonia [Time frame: Up to day 28]
• Hypoxemia (Sp02 <90%) [Time frame: Up to day 28]

Eligibility criteria

Inclusion criteria

• Enrolled in the initial prognostic screening component.
• Sick children with fever (axillary temperature>37.5ºC) or a history of fever (within the preceding 72h) or with suspected severe disease.
• 1m-<60 months of age.
• With an indication for admission, or having already been admitted to hospital due to their illness.
• With an sTREM-1 PoC result classifying their disease as of "moderate-high risk" ("yellow" or "red") upon study recruitment and within D3.
• Residents in the study area or willing to be contacted and traced during the study duration.
• Willing to sign an informed consent document.
• Willing to undergo and adhere to study procedures as explained in the IC document.

Exclusion criteria

• Admission to hospital for social reasons (and not on account of their disease).
• Children for which informed consent document has not been signed.
• Known allergy or contraindication to any of the study supplements including lactose intolerance or observing a lactose-free diet.
• Concurrent participation in any other clinical trial.
• Patient under NPO or "nothing by mouth" prescription .
• Contraindication for the insertion of a nasogastric tube (NGT) of for the enteral administration of drugs through the NGT in children who cannot tolerate by mouth.
• Critically sick patient whose prognosis is considered by the clinical researcher as fatal outcome in the following hours after screening.
• Any other condition determined by the investigators that makes it unlikely that the participant would complete the follow up until day 28 of study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Quadruple blind

Primary purpose

Treatment

Study locations

Ethiopia · 1 center

• Hararghe Health Research — Harar

Mozambique · 1 center

• Hospital Central de Maputo — Maputo

Identifiers

NCT: NCT06426147 · EChiLiBRiST CT2

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗