HumRes64953
|
SNCTP000005899
|
BASEC2023-D0106
|
NCT06344871
Exploratory study of NeuroLF, a medical trial product without CE marking for PET imaging of the human brain
Résumé de l'étude
For this study, patients will be recruited who are scheduled for a regular clinical PET scan. By participating, they will stay a little longer in the hospital during this single appointment, and an additional image will be taken on the NeuroLF prototype alongside the regular PET image. This will take up to one hour longer than the visit would normally last.
(BASEC)
Intervention étudiée
Brain PET scan
(BASEC)
Maladie en cours d'investigation
Functional diseases of the brain, e.g., Alzheimer's disease
(BASEC)
Critères de participation
• Ability to sit still in the pure head PET scanner for 15 minutes • You are scheduled for a regular brain PET examination as part of the clinical routine. • Male and female patients aged 18 to 80 years (BASEC)
Critères d'exclusion
• Contraindications for a PET examination, • Metal implants in the head, • Pregnant and breastfeeding women, (BASEC)
• Ability to sit still in the pure head PET scanner for 15 minutes • You are scheduled for a regular brain PET examination as part of the clinical routine. • Male and female patients aged 18 to 80 years (BASEC)
Critères d'exclusion
• Contraindications for a PET examination, • Metal implants in the head, • Pregnant and breastfeeding women, (BASEC)
Lieu de l’étude
Zurich
(BASEC)
Germany, Switzerland (ICTRP)
Sponsor
Positrigo AG
(BASEC)
Contact pour plus d'informations sur l'étude
Personne de contact en Suisse
Jannis Fischer
+41 44 5155331
jannis.fischer@clutterpositrigo.comPositrigo AG
(BASEC)
Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)
Commission cantonale de Zurich
(BASEC)
Date d'approbation du comité d'éthique
14.05.2024
(BASEC)
Identifiant de l'essai ICTRP
NCT06344871 (ICTRP)
Titre officiel (approuvé par le comité d'éthique)
EXPLORATORY STUDY OF NEUROLF, AN INVESTIGATIONAL MEDICAL DEVICE WITHOUT CE-MARKING FOR PET IMAGING OF THE HUMAN BRAIN (BASEC)
Titre académique
Exploratory Study of NeuroLF, an Investigational Medical Device Without CE Marking for PET Imaging of the Human Brain (ICTRP)
Titre public
Exploratory Study Using a New Head-only PET Scanner / ExploreNeuroLF (ICTRP)
Maladie en cours d'investigation
Brain Diseases (ICTRP)
Intervention étudiée
Device: NeuroLFDevice: Conventional PET scan (ICTRP)
Type d'essai
Interventional (ICTRP)
Plan de l'étude
Allocation: Non-Randomized. Intervention model: Single Group Assignment. Primary purpose: Diagnostic. Masking: None (Open Label). (ICTRP)
Critères d'inclusion/exclusion
Inclusion Criteria:
- Capable of giving Informed Consent as documented by signature (Appendix Informed
Consent Form).
- Ability to sit still in the head-only PET scanner for 15 minutes.
- Are scheduled to receive a regular brain PET scan as part of clinical routine.
- Male and Female patients 18 years to 80 years of age.
Exclusion Criteria:
- Contraindications to PET examination,
- Patient height smaller than 160 cm or taller than 200 cm,
- Patient weight more than 120 kg,
- Patient cannot sit upright for at least 15 minutes,
- Metal implants in the head,
- Pregnant or Breastfeeding women,
- Known or suspected non-compliance, drug or alcohol abuse,
- Inability to follow the procedures of the study, e.g. due to language problems,
psychological disorders, dementia, etc. of the participant,
- Participation in another study with investigational drug/device within the 30 days
preceding and during the present study,
- Previous enrolment into the current study,
- Enrolment of the investigator, his/her family members, employees and other dependent
persons. (ICTRP)
non disponible
Critères d'évaluation principaux et secondaires
PET Image of the Brain (ICTRP)
Ease of Placement (Usability);Usage of accessories for patient placement (Usability) (ICTRP)
Date d'enregistrement
non disponible
Inclusion du premier participant
non disponible
Sponsors secondaires
University of Zurich;University of Leipzig (ICTRP)
Contacts supplémentaires
Jannis Fischer, Dr., jannis.fischer@positrigo.com, +41445155331 (ICTRP)
ID secondaires
002 (ICTRP)
Résultats-Données individuelles des participants
non disponible
Informations complémentaires sur l'essai
https://clinicaltrials.gov/ct2/show/NCT06344871 (ICTRP)
Résultats de l'essai
Résumé des résultats
non disponible
Lien vers les résultats dans le registre primaire
non disponible