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CompletedNCT00215878Updated Jul 9, 2012

D-serine for Posttraumatic Stress Disorder Treatment

A Phase 2 interventional study of D-serine (~2g /day) in Posttraumatic Stress Disorder, sponsored by Herzog Hospital. Completed at 1 site in Israel. Open to participants aged 25 Years to 75 Years. Per ClinicalTrials.gov, last updated 2012-07-09.

Sponsored by Herzog Hospital · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
22
Allocation
Randomized
Ages
25 Years to 75 Years
Sex
All
01

Study 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.

02

Conditions studied

03

In context

Stress Disorders, Traumatic

1,147 studies on the registry are indexed under Stress Disorders, Traumatic; 108 are open to participants now.

This study's enrollment of 22 is below the median of 60 across 908 interventional studies indexed under Stress Disorders, Traumatic.

Browse Stress Disorders, Traumatic studies →

Lead sponsor

Herzog Hospital is the lead sponsor of 24 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Chronic PTSD (DSM-IV diagnosis)

Exclusion criteria

Exclusion Criteria:

  • Other psychiatric diagnosis
  • Substance abuse
  • Unstable medical condition
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
22 participants (actual)

Study arms

  • Placebo comparator
    1

    Adjuvant 6 weeks treatment with placebo (\~2g /day)

    Drug: D-serine (~2g /day)

  • Experimental
    2

    Adjuvant 6 weeks treatment with D-serine (\~2g /day)

    Drug: D-serine (~2g /day)

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)

06

What researchers measure

Primary outcomes

  1. CAPS scores

    Time frame: 6 week treatment

07

Study locations

1 site
  • Ezrat Nashim-Herzog Memorial Hospital
    Jerusalem, 91351, Israel
08

References and documents

Publications

  • Heresco-Levy U, Vass A, Bloch B, Wolosker H, Dumin E, Balan L, Deutsch L, Kremer I. Pilot controlled trial of D-serine for the treatment of post-traumatic stress disorder. Int J Neuropsychopharmacol. 2009 Oct;12(9):1275-82. doi: 10.1017/S1461145709000339. Epub 2009 Apr 15. PubMed 19366490 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00215878
Lead sponsor
Herzog Hospital
Responsible party
Heresco-Levi Uriel (Principal Investigator, Herzog Hospital) — Principal investigator
First posted
Sep 22, 2005
Start date
Aug 2003
Primary completion
May 2008
Completion
May 2008
Last update
Jul 9, 2012

Study contacts

Uriel Heresco-Levy, M.D
principal investigator · Ezrat Nashim-Herzog Memorial Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.

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