Healthy Volunteer Clinical Trial
Official title:
Repetitive Transcranial Magnetic Stimulation Equipment Testing and Pilot Study
Background:
- Brain stimulation called repetitive transcranial magnetic stimulation (rTMS) may help
people quit drugs. Researchers want to study how it works in healthy people first.
Objective:
- To learn how to use rTMS to stimulate a brain area and to see how it affects brain function
and thinking.
Eligibility:
- Healthy, right-handed adults ages 18-55.
Design:
- Participants will be screened under another protocol.
- They will have 4-11 study visits.
- To start each visit, participants will have:
- Physical exam.
- Urine sample.
- Breath tests for alcohol and cigarette smoke.
- Questions about drug use and medications.
- Visit 1: participants will have:
- Single TMS pulses on the head to determine the right strength. They will wear earplugs
and a cap. A wire coil will be placed on the head and an electrical current will go
through it. Participants may perform simple muscle movements. They will repeat the
procedures wearing another coil, in a helmet.
- A few TMS pulses to show how rTMS feels.
- A practice thinking task, maybe in a scanner that looks and sounds like a magnetic
resonance imaging (MRI) scanner but does not take pictures. The MRI scanner is a metal
cylinder surrounded by a strong magnetic field. The participant will lie on a table that
slides in and out of the cylinder.
- They may have a real MRI scan.
- Visits 2-11, participants will:
- Complete two questionnaires.
- Get varied rTMS stimulation. Their heart rate and blood pressure may be monitored.
- Have their vital signs checked.
- They may perform thinking tasks at a computer, in a mock scanner, or in an MRI scanner.
They may just lie still in the MRI scanner.
Objective: To establish an effective repetitive transcranial magnetic stimulation (rTMS)
protocol for stimulating circuits relevant for addiction. Specifically, we will develop
stimulation parameters and outcome measures for rTMS of the anterior cingulate cortex (ACC)
with a specialized TMS coil: the HAC coil (Brainsway Ltd.). Various parameters of rTMS
stimulation (frequency and intensity) will be varied, and the sensitivity of behavioral tasks
and MRI measures to this stimulation will be determined. The objective of this protocol is
therefore to allow for the development, assessment and refinement of rTMS parameters for
stimulating ACC targets. In addition, outcome measures will be developed to capture the
effects of this stimulation. Results from this development protocol will be applied to
subsequent cognitive imaging protocols.
Study population: Up to 50 healthy, non-smoking adults will be tested in several conditions
over up to two weeks. Subjects must fit exclusion/inclusion criteria for TMS and MRI. We
expect 140 subjects to be enrolled to arrive at a number of 50 who complete the protocol.
Design: Within-subject design with each subject completing up to 10 rTMS sessions.
Outcome measures: In a first phase, the outcome measure will be the behavioral response on a
task that relies on the ACC. In a second phase, outcome measures will be the effects on MR
measures. These will include task-related blood oxygen level-dependent (BOLD) responses, as
well as resting state BOLD functional magnetic resonance imaging (fMRI). Other MR measures,
such as magnetic resonance spectroscopy (MRS) and arterial spin labeling (ASL), will also be
explored as potential biomarkers.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT06326723 -
Investigate the PK, Safety, and Tolerability After Single and Multiple Dose Daridorexant in Chinese Healthy Subjects
|
Phase 1 | |
Recruiting |
NCT00001367 -
Diagnosis and History Study of Patients With Different Neurological Conditions
|
||
Completed |
NCT02699710 -
Effect of Food, Rabeprazole, Methotrexate and Formulation on the Pharmacokinetics (PK) of GDC-0853 and the Effect of GDC-0853 on the PK of Methotrexate in Healthy Subjects
|
Phase 1 | |
Not yet recruiting |
NCT06441916 -
Bioequivalence Study of Dabigatran Etexilate Capsules 150 mg in Healthy Thai Volunteers Under Fasting Conditions
|
Phase 1 | |
Completed |
NCT03771586 -
A Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketamine Challenge in Healthy Subjects
|
Phase 1 | |
Not yet recruiting |
NCT06337422 -
Bioequivalence Study of Generic Celecoxib 200 mg Capsules
|
Phase 1 | |
Completed |
NCT03302182 -
Bioequivalence Study of Ritonavir Versus NORVIR in Healthy Chinese Subjects
|
Phase 1 | |
Completed |
NCT05049343 -
Study of SAGE-904 Using a Ketamine Challenge to Evaluate Electrophysiology, Safety, Tolerability, and Pharmacokinetics in Healthy Participants
|
Phase 1 | |
Recruiting |
NCT01629108 -
Normal Values in Hearing and Balance Testing
|
||
Completed |
NCT02947854 -
Study to Assess Safety, Tolerability and Immune Response of Fimaporfin-induced Photochemical Internalisation of Antigen/Adjuvant
|
Phase 1 | |
Completed |
NCT02534870 -
Pharmacokinetics and Safety of the Co-administration of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 in Healthy Chinese Subjects
|
Phase 1 | |
Completed |
NCT02224053 -
Drug-Drug Interaction Study With AZD9291 and Omeprazole in Healthy Volunteers
|
Phase 1 | |
Completed |
NCT01711762 -
A Pharmacokinetics Study of Radioactive-Labeled GDC-0973 in Healthy Male Volunteers
|
Phase 1 | |
Completed |
NCT01676584 -
A Study of Single Dose RO6811135 in Healthy Volunteers
|
Phase 1 | |
Completed |
NCT01697436 -
A Bioequivalence Study of an Oral Solution of Copegus (Ribavirin) Compared to Copegus Tablets
|
Phase 1 | |
Completed |
NCT01684891 -
A 28-Day Pharmacokinetics Study of RG1662 in Healthy Male Volunteers
|
Phase 1 | |
Completed |
NCT01579149 -
A Phase I Dose Escalation Study of Plerixafor in Healthy Subjects of Japanese Descent
|
Phase 1 | |
Completed |
NCT01591850 -
A Drug-Drug Interaction Study of Ketoconazole, Rifampicin and Ritonavir-Boosted Atazanavir With Single-Dose RO5093151 in Healthy Volunteers
|
Phase 1 | |
Completed |
NCT01461967 -
A Study on Safety, Pharmacokinetics and Pharmacodynamics of RO5508887 in Healthy Volunteers
|
Phase 1 | |
Completed |
NCT02547259 -
Influence of Emotion in a Test Run Forgetfulness
|
N/A |