Healthy Clinical Trial
Official title:
Development of Automated Analysis to Electroencephelogram (EEG) Data in Patients Treated at the Sagol Hyperbaric Medicine and Research Center at the Years 2017-2019 - A Retrospective Study
NCT number | NCT04095377 |
Other study ID # | 0292-18 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 24, 2019 |
Est. completion date | February 14, 2022 |
Verified date | March 2019 |
Source | QuantalX Neuroscience |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
DELPhI software developed for the analysis of EEG recordings in response to magnetic stimulation in relation to clinical data.
Status | Completed |
Enrollment | 875 |
Est. completion date | February 14, 2022 |
Est. primary completion date | February 14, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Subjects over the age of 18. - Subjects that performed at least one EEG test as a part of their hyperbaric treatment at Sagol center Asaf-Harophe. Exclusion Criteria: - Subjects with no EEG test or that their EEG recording is in pure quality, not allowing analysis of the data. |
Country | Name | City | State |
---|---|---|---|
Israel | Asaf-Harophe | Rishon LeZion |
Lead Sponsor | Collaborator |
---|---|
QuantalX Neuroscience |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Defining Plasticity (the ratio between excitatory to inhibitory brain response) Means and STD in each cohort. | Measure of the mean and STD Plasticity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Connectivity (dispersion of brain signal) Means and STD in each cohort. | Measure of the mean and STD Connectivity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Plasticity (the ratio between excitatory to inhibitory brain response) standard error (SEM) in each cohort. | Measure of the standard error (SEM) of Plasticity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Connectivity (dispersion of brain signal) standard error (SEM) in each cohort. | Measure of the standard error (SEM) of Connectivity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Plasticity (excitation/inhibition brain response) coefficient of variation (CV%) in each cohort. | Measure of the coefficient of variation (CV%) of Plasticity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Connectivity (dispersion of brain signal) coefficient of variation (CV%) in each cohort. | Measure of the coefficient of variation (CV%) of Connectivity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Plasticity (excitation/inhibition brain response) minimum, median, maximum in each cohort. | Measure of the minimum, median, maximum of Plasticity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Connectivity (dispersion of brain signal) minimum, median, maximum in each cohort. | Measure of the minimum, median, maximum of Connectivity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Plasticity (excitation/inhibition brain response) 95% confidence interval in each cohort. | Measure of the 95% confidence interval of Plasticity of each cohort. | through study completion, an average of 1 year | |
Primary | Defining Connectivity (dispersion of brain signal) 95% confidence interval in each cohort. | Measure of the 95% confidence interval of Connectivity of each cohort. | through study completion, an average of 1 year |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06052553 -
A Study of TopSpin360 Training Device
|
N/A | |
Completed |
NCT05511077 -
Biomarkers of Oat Product Intake: The BiOAT Marker Study
|
N/A | |
Recruiting |
NCT04632485 -
Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
|
||
Completed |
NCT05931237 -
Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults
|
N/A | |
Completed |
NCT04527718 -
Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers
|
Phase 1 | |
Terminated |
NCT04556032 -
Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women
|
N/A | |
Completed |
NCT04998695 -
Health Effects of Consuming Olive Pomace Oil
|
N/A | |
Completed |
NCT04107441 -
AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects
|
Phase 1 | |
Completed |
NCT04065295 -
A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225
|
Phase 1 | |
Completed |
NCT01442831 -
Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects
|
Phase 1 | |
Terminated |
NCT05934942 -
A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood
|
Phase 1 | |
Recruiting |
NCT05525845 -
Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI
|
N/A | |
Completed |
NCT05515328 -
A Study in Healthy Men to Test How BI 685509 is Processed in the Body
|
Phase 1 | |
Completed |
NCT05030857 -
Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects
|
Phase 1 | |
Completed |
NCT04967157 -
Cognitive Effects of Citicoline on Attention in Healthy Men and Women
|
N/A | |
Recruiting |
NCT04714294 -
Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers
|
Phase 1 | |
Recruiting |
NCT04494269 -
A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls
|
Phase 1 | |
Completed |
NCT04539756 -
Writing Activities and Emotions
|
N/A | |
Recruiting |
NCT04098510 -
Concentration of MitoQ in Human Skeletal Muscle
|
N/A | |
Completed |
NCT03308110 -
Bioavailability and Food Effect Study of Two Formulations of PF-06650833
|
Phase 1 |