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Tryptophan, Serotonin and Kynurenine in Septic Shock

Tryptophan, Serotonin and Kynurenine in Septic Shock

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00684736
Acronym
TSK
Enrollment
30
Registered
2008-05-28
Start date
2004-06-30
Completion date
2008-04-30
Last updated
2008-08-08

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

Conditions

Shock, Septic

Keywords

septic shock, shock, serotonin, kynurenine, tryptophan

Brief summary

Septic shock is a major cause of mortality and morbidity worldwide. Serotonin (5-HT) is released by activated platelets into the circulation, and is mediator of endothelial dysfunction. 5-HT metabolism is known in immune system via specific 5-HT receptor, also in effects on the peripheral nervous system. Kinetic of 5-HT, tryptophan, kynurenine, MAO activity and IDO activity in human septic shock was never investigated.

Interventions

None listed

Sponsors

Versailles Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age above or equal to 18 years * Strong presumption clinical sepsis * Need for mechanical ventilation * Body temperature above 38°C or below 36°C * Heart rate above 90 bpm * Systolic blood pressure of \<90mm Hg despite adequate fluid replacement or a need for vasopressors less than 3 hours * Presence of at least one of the following criteria: * Ratio of arterial oxygen tension over inspired fraction of oxygen of less than 300 mm Hg * Urinary output below 0.5 mL per kg of bodyweight per h or below 30 mL/h (for at least 1 h) * Arterial lactate concentration above 2 mmol/L * Consent signed

Exclusion criteria

* Age below 18 years * Pregnancy * Underlying disease with a poor prognosis, a life expectancy of less than 24 hours * Depression or melancholy * Neuropsychiatric diseases: Seizure, manic psychosis, Migraine, or Drug addiction * Neuroendocrine tumors * Obstructive cardiomyopathy or acute myocardial ischaemia * Pulmonary embolism * Advanced stage cancer, malignant haemopathy, or AIDS with a decision to withhold or withdraw aggressive therapies * Inclusion in another clinical trial * Patient who receive before inclusion one of the following treatment known to modify serotonin level: almotriptan, amitriptyline, amoxapine, citalopram, clomipramine, clozapine, desipramine, dihydroergotamine, dolasetron, dosulepin, doxepin, eletriptan, ergotamine, flunarizine, fluoxetine, fluvoxamine, granisetron, imipramine, indoramin, interferon Alfa, interferon alfacon-1, interferon beta, iproniazid, maprotiline, methysergide, mianserin, Milnacipran, mirtazapine, moclobemide, naratriptan, olanzapine, ondansetron, oxetorone, paroxetine, pizotifen, risperidone, sertraline, sumatriptan, tianeptine, trimipramine, tropisetron, venlafaxine,viloxazine, zolmitriptan. * No consent

Design outcomes

Primary

MeasureTime frame
Kinetics of 5-HT, 5-HIAA, kynurenine, tryptophan, HVA, VMA, DOPAC, Oestradiol, Cotinine and vasopressorsDay-1, Day-2, Day-3, Day-7 and Day-14

Secondary

MeasureTime frame
Mortality28-day

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026