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Study of Freefol-MCT PKPD in Healthy Volunteers

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02384720
Enrollment
60
Registered
2015-03-10
Start date
Unknown
Completion date
Unknown
Last updated
2016-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

The purpose of this study is to analysis PKPD of Freefol-MCT and to investigate relationship between the concentration of Freefol-MCT and the index which signaly analyzes those: EEG, EEG approximate entropy, systolic BP, saturation wave form and invasive BP wave form.

Interventions

OTHERAge: 20-40years
OTHERAge: 41-64years
OTHERAge: ≥65years

Sponsors

Daewon Pharmaceutical Co., Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults males/Females aged over 20years * Health screening examination within 60 days of the start (Interview, vital signs , 12-lead ECG, blood tests, urinalysis) . * The applicant who agreed in writing by told an explanation enough about the characteristics of the study drug, the purpose of the test and the details.

Exclusion criteria

* Subjects with clinically significant disease or history such as Liver, kidney, gastrointestinal, respiratory, musculoskeletal, endocrine, nervous psychiatric, blood tumor system and cardiovascular. (In particular, bronchial asthma, severe hepatic, renal failure, severe blood disorders, severe myasthenia gravis, cardiac dysfunction, peptic ulcer, etc.) * Who had acute disease or organ dysfunction within four weeks of the start of the test. * Who had significant hematologic disorders or donate whole blood within two months of the start of the test. * Significant neuropsychiatric or more. * Continued drug abuse. * Who has a history of drug and other hypersensitivity reactions. * Positive at Type B / C hepatitis , syphilis tests (VDRL), if in AIDS antibody test * Who took other clinical medicine within two months of the start of the test. * Who smokes or drinks within two weeks after dosing. * Who takes drugs regularly other than the mineral claim or vitamin. However, it depends on judgment of the researchers.

Design outcomes

Primary

MeasureTime frame
Non- compartment pharmacokinetic parameters1200 minutes
Compartment pharmacokinetic parameters1200 minutes
BIS1200 minutes
SBP1200 minutes
E01200 minutes
Emax1200 minutes
Ce501200 minutes
ke01200 minutes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026