Clinical trial

Novel in Vivo Synaptic Imaging in Experienced Meditators

Name
2000030601
Description
To utilize positron emission tomography (PET) imaging to characterize the distribution of (aka \[11C\]APP311at the Yale PET Center) in cortical and subcortical areas in experienced meditators compared to non-meditating controls.
Trial arms
Trial start
2022-04-21
Estimated PCD
2024-08-31
Trial end
2024-08-31
Status
Recruiting
Phase
Early phase I
Treatment
Radiotracer
A novel SV2A imaging tracer which is used in conjunction with positron emission tomography scans.
Arms:
Aim 1
Other names:
[11C]APP311, [11C]UCB-J
Size
20
Primary endpoint
Analyzing positron emission tomography images in conjunction with magnetic resonance data
Up to two years
Eligibility criteria
Inclusion Criteria: * Age 28-70 years * Voluntary, written, informed consent * Physically healthy by medical history, physical, ECG and laboratory examinations * At least 10 years and 5,000 hours of regular meditation practice * For females, non-lactating, no longer of child-bearing potential or agree to practice effective contraception during the study, as well as a negative serum pregnancy (β-HCG) test at screening, and negative urine pregnancy on PET scanning days. Exclusion Criteria: * A history of significant psychiatric, medical (e.g., cardiovascular, renal) or neurological (e.g., cerebrovascular, seizure, traumatic brain injury) illness that is unstable and/or might affect the study objectives. * Current or history of substance dependence (e.g., alcohol, nicotine, opiates, sedative hypnotics, etc.) * Subjects with history of prior radiation exposure for research purposes within the past year such that participation in this study would place them over FDA limits for annual radiation exposure. This guideline is an effective dose of 5 rem received per year. * Subjects with current, past or anticipated exposure to radiation in the work place within one year of proposed research PET scans that in combination with the study tracer would result in a cumulative exposure that exceeds recommended exposure limits. * Medical contraindications to participation in a magnetic resonance imaging procedure (e.g., ferromagnetic implants/foreign bodies, claustrophobia, cardiac pacemaker, prosthetic valve, otologic implant, etc.) * History of a bleeding disorder or are currently taking anticoagulants (such as Coumadin, Heparin, Pradaxa, Xarelto). * Medications that effect SV2A binding (e.g., levetiracetam).
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'BASIC_SCIENCE', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 20, 'type': 'ESTIMATED'}}
Updated at
2023-07-14

1 organization

1 product

2 indications

Organization
Yale University
Indication
Behaviour
Indication
health