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Recruiting NCT07251049

NCT07251049 Acute Infectious Encephalitis and Myelitis in Guadeloupe by New Generation Sequencing

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Clinical Trial Summary
NCT ID NCT07251049
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire de la Guadeloupe
Condition Acute Encephalitis
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2023-11-16
Primary Completion 2028-11-16

Eligibility & Interventions

Sex All sexes
Min Age 28 Days
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2023-11-16 with a primary completion date of 2028-11-16.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

: Encephalitis or myelitis is defined as the inflammatory or infectious involvement of the cerebral parenchyma or spinal cord. When an infectious origin is suspected, the germ is not always identified. Next-generation sequencing could be used to correct an etiological diagnosis of these severe conditions in Guadeloupe. The rate of cases for which the infectious agent is not identified encourages continued diagnostic efforts, with the objective of identifying new pathogens or emerging pathogens, some of which may be more specific in the tropics.

Eligibility Criteria

Inclusion Criteria: * We selected the following eligibility criteria for patients with acute encephalitis: * Patient of at least 28 days of life * With acute onset of symptoms for more than 24 hours * A major criterion among the following: * a disorder of consciousness or alertness * memory disorder * lethargy * modification of personal or behavioral disorder, irritability * confusion, disorientation in time or space \- At least two of the following minor criteria: * temperature above 38 ° C * new onset focal neurological deficit * epileptic crisis * biological abnormality of CSF (≥ 5 Leukocytes / mm3, protein ≥ 0.40 g / L) * partial or general epileptic seizure (s) not attributable to pre-existing epileptic disease and / or a recent focal neurological symptom * brain imaging suggestive of encephalitis, with EEG abnormalities suggestive of encephalitis * And absence of alternative diagnosis (intoxication, metabolic encephalopathy) * Persons affiliated or benefiting from a social security scheme; * Having given free, informed, written and signed consent by the patient or his legal representative (no later than the day of inclusion and prior to any review required by the research); * Eligibility criteria for Acute Transverse Myelitis Patients: * Patient of at least 28 days of life * Acute onset of symptoms for more than 24 hours * Medullary focal abnormality, responsible for motor, sensory or autonomic symptoms * contrast enhancement on bone marrow MRI and / or abnormal CSF (≥ 5GB / mm3, protein uptake ≥ 0.40 g / L) * Evolution between nadir and maximum symptoms, less than 4 weeks * Persons affiliated or benefiting from a social security scheme; * Having given free, informed, written and signed consent by the patient or his legal representative (no later than the day of inclusion and prior to any review required by the research); Exclusion Criteria: * Primary vasculitis of the central nervous system or a documented specific impairment in an autoimmune condition * Cerebral thrombophlebitis if not associated with encephalitis * Meningitis without clinical or paraclinical argument for cerebral parenchymal involvement * Pyogenic abscess * Cerebral or spinal abscess * Tumoral or hematological pathology of the central nervous system * Toxic or metabolic encephalopathy * Transverse myelitis with vascular or traumatic origin * Known chronic infection with HTLV virus

Contact & Investigator

Central Contact

Val"érie HAMONY-SOTER

✉ valerie.soter@chu-guadeloupe.fr

📞 +590 590 93 46 77

Principal Investigator

Hugo CHAUMONT, Doctor

PRINCIPAL INVESTIGATOR

CHU de la Guadeloupe

Frequently Asked Questions

Who can join the NCT07251049 clinical trial?

This trial is open to participants of all sexes, aged 28 Days or older, studying Acute Encephalitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07251049 currently recruiting?

Yes, NCT07251049 is actively recruiting participants. Contact the research team at valerie.soter@chu-guadeloupe.fr for enrollment information.

Where is the NCT07251049 trial being conducted?

This trial is being conducted at Pointe-à-Pitre, Guadeloupe.

Who is sponsoring the NCT07251049 clinical trial?

NCT07251049 is sponsored by Centre Hospitalier Universitaire de la Guadeloupe. The principal investigator is Hugo CHAUMONT, Doctor at CHU de la Guadeloupe. The trial plans to enroll 100 participants.

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