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D-serine for Posttraumatic Stress Disorder Treatment

D-serine for Posttraumatic Stress Disorder Treatment

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00215878
Enrollment
22
Registered
2005-09-22
Start date
2003-08-31
Completion date
2008-05-31
Last updated
2012-07-09

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

Conditions

Posttraumatic Stress Disorder

Brief summary

The aim of this study is to asses the effects of the NMDA receptor full agonist D-serine while used as adjuvant treatment for individuals suffering from chronic posttraumatic stress disorder (PTSD). Dysfunction of neurotransmission mediated at NMDA receptor plays a cardinal role in the pathophysiology of PTSD and PTSD patients typically suffer from cognitive dysfunctions and avoidance& depressive symptomatology that may be mediated by NMDA receptor function deficits. Thus, enhancement of NMDA activity by using D-serine may be beneficial in the treatment of PTSD. The study design involves two 6 week periods during which the participants will be randomly assigned to receive treatment with D-serine (\ 2g /dy)and placebo. This design allows each participant the opportunity to respond to the experimental treatment.

Interventions

DRUGD-serine (~2g /day)

Two 6 weeks treatment arms under a cross over design. In one arm adjuvant treatment with experimental medication (D-serine \ 2g /day), in the second arm adjuvant treatment with placebo (\ 2g /day)

Sponsors

Herzog Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

• Chronic PTSD (DSM-IV diagnosis)

Exclusion criteria

* Other psychiatric diagnosis * Substance abuse * Unstable medical condition

Design outcomes

Primary

MeasureTime frame
CAPS scores6 week treatment

Countries

Israel

Outcome results

None listed

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