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UnknownNCT01008098

Neuroprotective/Neurotrophic Effect of Lexapro® in Patients With PTSD

Medication studyAges 18–65South Korea
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 65 years.

Listed locations
Seoul, South KoreaSee all locations and recruitment
Activities
Medication described in the protocol
Compensation
Payment and expense reimbursement have not been verified.

What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateNovember 2008
Recruitment status
Unknown
Enrollment listed in the registry
26
Sponsor
Seoul National University Hospital
Sponsor type
Hospital / academic medical center
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
South Korea
Age range
From 18 Years to 65 Years
Official registry ID
NCT01008098
Official title
Show the full official title

Neuroprotective/Neurotrophic Effect of Lexapro® in Patients With Posttraumatic Stress Disorder

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Recruitment & locations

Status unknown

Seoul

Checked Official study record (opens in a new tab)

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Seoul National University Hospital, a hospital or academic medical center.

Does this study involve medication?

Yes. The study involves medication, including escitalopram (lexapro).

Who can participate?

Listed age limits: 18 years to 65 years.

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