CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


L-citrullineWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (3)


Name (Synonyms) Correlation
drug2786 consultation Wiki 1.00
drug262 Azithromycin Wiki 0.17
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D055371 Acute Lung Injury NIH 0.10
D012127 Respiratory Distress Syndrome, Newborn NIH 0.10
D012128 Respiratory Distress Syndrome, Adult NIH 0.09
D011014 Pneumonia NIH 0.06

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.06

There is one clinical trial.

Clinical Trials


1 CACOLAC : Randomized Trial of Citrulline Administration in the Hospital Patient in Intensive Care for COVID-19 Acute Respiratory Distress Syndrome

Respiratory involvement of SARS-CoV2 leads to acute respiratory distress syndrome (ARDS) and significant immunosuppression (lymphopenia) exposing patients to long ventilation duration and late mortality linked to the acquisition of nosocomial infections. Lymphopenia characteristic of severe forms of ARDS secondary to SARS-CoV2 infection may be linked to expansion of MDSCs and arginine depletion of lymphocytes. Severe forms of COVID-19 pneumonitis are marked by persistent ARDS with acquisition of nosocomial infections as well as by prolonged lymphocytic dysfunction associated with the emergence of MDSC. It has been found in intensive care patients hypoargininaemia, associated with the persistence of organ dysfunction (evaluated by the SOFA score), the occurrence of nosocomial infections and mortality. Also, it has been demonstrated that in these patients, the enteral administration of ARG was not deleterious and increased the synthesis of ornithine, suggesting a preferential use of ARG by the arginase route, without significant increase in argininaemia nor effect on immune functions. L-citrulline (CIT), an endogenous precursor of ARG, is an interesting alternative to increase the availability of ARG. Recent data demonstrate that the administration of CIT in intensive care is not deleterious and that it very significantly reduces mortality in an animal model of sepsis, corrects hypoargininemia, with convincing data on immunological parameters such as lymphopenia, which is associated with mortality, organ dysfunction and the occurrence of nosocomial infections. The availability of ARG directly impacts the mitochondrial metabolism of T lymphocytes and their function. The hypothesis is therefore that CIT supplementation is more effective than the administration of ARG to correct hypoargininaemia, decrease lymphocyte dysfunction, correct immunosuppression and organ dysfunction in septic patients admitted to intensive care. The main objective is to show that, in patients hospitalized in intensive care for ARDS secondary to COVID-19 pneumonia, the group of patients receiving L-citrulline for 7 days, compared to the group receiving placebo, has a score of organ failure decreased on D7 (evaluated by the SOFA score) or by the last known SOFA score if the patient has died or been resuscitated.

NCT04404426 ARDS Secondary to COVID-19 Pneumonia Dietary Supplement: L-citrulline Other: Placebo
MeSH:Pneumonia Respiratory Distress Syndrome, Newborn Respiratory Distress Syndrome, Adult Acute Lung Injury
HPO:Pneumonia

Primary Outcomes

Description: SOFA score for organ failures on D7 or last known SOFA score if the patient has died or been resuscitated

Measure: SOFA

Time: Day 7

Secondary Outcomes

Description: Number and phenotype of lymphocytes on days 1, 3, 7, 10 and 14

Measure: Number and phenotype of lymphocytes

Time: Days 1, 3, 7, 10 and 14

Description: Monocytic expression HLA-DR (Flow cytometry) on days 1, 3, 7, 10 and 14

Measure: HLA-DR

Time: Days 1, 3, 7, 10 and 14

Description: Number of Myeloid-derived suppressor cells (Flow cytometry) on days 1, 3, 7, 10 and 14

Measure: Number of Myeloid-derived suppressor cells

Time: Days 1, 3, 7, 10 and 14

Description: Plasma cytokines / chemokines (IL-6, IL-8, IL-10, IL-7, CXCL10, G-CSF, TNF-alpha, IFN-β) at days 1, 3, 7, 10 and 14

Measure: Plasma cytokines / chemokines

Time: Days 1, 3, 7, 10 and 14

Description: Diversity of the repertoire T at days 1, 3, 7, 10 and 14

Measure: Repertoire T

Time: Days 1, 3, 7, 10 and 14

Description: T lymphocyte exhaustion: measurement of lymphocyte apoptosis and lymphocyte proliferation on days 1, 3, 7, 10 and 14

Measure: Lymphocyte T exhaustion

Time: Days 1, 3, 7, 10 and 14

Description: Measurement of mitochondrial activity (measurement of the number of mitochondria and their membrane potential, measurement of the expression of Beclin1) on days 1, 3, 7, 10 and 14

Measure: Mitochondrial activity

Time: Days 1, 3, 7, 10 and 14

Description: Plasma amino acids (arginine and its metabolites (ornithine, glutamate, glutamine, citrulline, proline) and tryptophan / kynurenine) on days 1, 3, 7, 10 and 14

Measure: Plasma amino acids

Time: Days 1, 3, 7, 10 and 14

Description: SOFA score of organ failures on days 3, 7, 10 and 14

Measure: SOFA

Time: Days 3, 7, 10 and 14

Description: Duration of hospitalization in intensive care (days), up to day 28 maximum

Measure: Duration of hospitalization in intensive care

Time: Day 28

Description: Duration of hospital stay in hospital (days), up to day 28 maximum

Measure: Duration of hospital stay in hospital

Time: Day 28

Description: Duration of mechanical ventilation (days), up to day 28 maximum

Measure: Duration of mechanical ventilation

Time: Day 28

Description: Mortality in intensive care on day 28

Measure: Mortality in intensive care on day 28

Time: Day 28

Description: Hospital mortality on day 28

Measure: Hospital mortality on day 28

Time: Day 28

Description: Measurement of the presence of SARS-CoV2 in the tracheal aspiration by PCR on days 1, 3, 7, 10 and 14

Measure: Measurement of the presence of SARS-CoV2

Time: Days 1, 3, 7, 10 and 14

Description: Incidence of nosocomial infections during the intensive care unit (maximum D28). The diagnosis of nosocomial infections will be made according to the definitions of nosocomial infections of the CDC. An independent committee of experts will validate or not the infections

Measure: Nosocomial infections

Time: D28

Description: Number of days of exposure to each antibiotic per 1000 days of hospitalization (maximum day 28).

Measure: Number of days of exposure to each antibiotic per 1000 days of hospitalization

Time: Day 28


Related HPO nodes (Using clinical trials)