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Facilitating effects of valproate on reconsolidation of fear extinction

Facilitating effects of valproate on reconsolidation of fear extinction

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CRIS
Registry ID
KCT0009483
Enrollment
92
Registered
2024-05-29
Start date
2024-05-27
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

None listed

Interventions

Drug : Group 1. Administration of trial drug and 3 hours standing: Extinction past 3 hours after fear memory reactivation. Oral administration of a Promag Tablet 500mg (Magnesium Valproate) one time 3

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Participants provided with an explanation of the study and written consent. - Participants with uncorrected visual acuity of -8.0 to -2.0 diopters (no restrictions for corrected vision with glasses or lenses). - Participants not currently having administered any treatment medication and in physical health.

Exclusion criteria

Exclusion criteria: - Carefully considered group of Biolamin Tablet: patients currently taking L-dopa, patients with hyperoxaluria, or pregnant or lactating women. - Individuals with hypersensitivity to polyvitamin (with vitamine B1, B2, B6, B12, C, or E) - Individulas not classified as healthy subjects through clinical examination. - Individuals with organic brain damage or a history of head and neck trauma. - Patients currently undergoing psychiatric treatment or with a psychiatric history. - Individuals anticipating surgery or procedures which could interfere the study procedures. - Carefully considered and contraindicated group of Promag Tablet: patients with liver disease or impairment, renal failure or low protein levels, blood clotting disorders or low platelet count, a history of bone marrow damage or potential patients, or currently pregnant or potentially pregnant women. - Individuals with a history of adverse reactions to valproate. - Individuals with difficulty in oral mication intake. - Researchers directly involved in the present clinical study, researchers' families, employees of the research institution, and their families.

Design outcomes

Primary

MeasureTime frame
Physiological responses including skin conductance response, electrocardiogram, respiration, and heart rate for each threat condition of stimuli and group;EEG (electroencephalogram) responses for each threat condition of stimuli and group

Secondary

MeasureTime frame
Subjective rating scores toward stimuli including risk assessment, valence, arousal, fear evaluation for each threat condition of the stimuli and group

Countries

Korea, Republic of

Contacts

Public ContactMinhee Kim

Seoul National University Hospital

mhkim8313@gmail.com+82-2-2939-8313

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026