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Recruiting NCT06463093

NCT06463093 Differential Diagnosis of Cognitive Disorders of Psychiatric or Neurodegenerative Origin

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Clinical Trial Summary
NCT ID NCT06463093
Status Recruiting
Phase
Sponsor Central Hospital, Nancy, France
Condition Neurocognitive Disorders
Study Type OBSERVATIONAL
Enrollment 20 participants
Start Date 2024-11-30
Primary Completion 2025-01-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
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 20 participants in total. It began in 2024-11-30 with a primary completion date of 2025-01-30.

⚠ 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

The aim of the research is to analyze whether 18F-FDG PET helps in the diagnosis and therefore in the management of the patient.

Eligibility Criteria

Inclusion Criteria: * Adult patients with cognitive impairment * Positron emission tomography with flurodeoxyglucose labeled with fluorine 18 carried out in the course of care Exclusion Criteria: * Patients objecting to the collection of their data

Contact & Investigator

Central Contact

Antoine VERGER, MD, PhD

✉ a.verger@chru-nancy.fr

📞 0383153911

Frequently Asked Questions

Who can join the NCT06463093 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Neurocognitive Disorders. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06463093 currently recruiting?

Yes, NCT06463093 is actively recruiting participants. Contact the research team at a.verger@chru-nancy.fr for enrollment information.

Where is the NCT06463093 trial being conducted?

This trial is being conducted at Vandœuvre-lès-Nancy, France.

Who is sponsoring the NCT06463093 clinical trial?

NCT06463093 is sponsored by Central Hospital, Nancy, France. The trial plans to enroll 20 participants.

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