Phase 2
Completed N=24
Zonisamide in Addition to E-CPT-C for Veterans With PTSD and Comorbid Alcohol Dependence
Source: ClinicalTrials.gov NCT01847469 ↗Enrolled (actual)
24
Serious AEs
12.5%
Results posted
Mar 2020
Primary outcomePrimary: Number of Drinking Days — 46.87; 51.00; 7.44; 17.33 days
Summary
This is a randomized, controlled trial with 50 veterans diagnosed with post-traumatic stress disorder (PTSD) and comorbid alcohol dependence. Veterans will be randomized to receive either zonisamide (400 mg) or placebo for 12 weeks in a double blind fashion. Randomization will be done using 3:1 ratio and will be performed by our research pharmacy using a random assignment in blocks of 4- 3 will be assigned to active medication and 1 to placebo. Medication will be titrated over a 6 week titration phase followed by a 6 week treatment phase. All veterans will receive E-CPT-C therapy for the 12 weeks of treatment; E-CPT-C will be provided by trained and qualified clinicians with extensive experience providing E-CPT-C. Veterans will be recruited primarily through advertisement, but also through the clinical facilities at the VA and from other collaborators.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Drinking Days |
46.87; 51.00; 7.44; 17.33 | — |
| PRIMARY Number of Heavy Drinking Days |
43.94; 31.50; 5.50; 4.16 | — |
| PRIMARY Clinician-Administered PTSD Scale (CAPS) Total Score |
67.33; 72.83; 30.83; 23.80 | — |
Eligibility Criteria
Inclusion Criteria
- Current alcohol dependence, as determined by a structured clinical interview (Structured Clinical Interview for DSM-IV Axis I Disorders) (SCID)
- Current PTSD as determined by a structured clinical interview (SCID)
- Veterans with current alcohol dependence, with at least one recent episode of heavy drinking over the past 14 days.
- Medically and neurologically healthy on the basis of history, physical examination, EKG, screening laboratories
- For women, negative pregnancy test and use of acceptable method of contraception
Exclusion Criteria
- Females who are pregnant or lactating.
- Veterans with a current unstable medical condition such as neurological, cardiovascular, endocrine, renal, liver, or thyroid pathology, which in the opinion of the physician would preclude the subject from fully cooperating or be of potential harm during the course of the study
- Veterans who meet current SCID criteria for a major Axis I diagnosis (Bipolar Disorders, Schizophrenia and Schizophrenia-type Disorders).
- History of substance dependence (other than alcohol, tobacco or cannabis) by DSM-IV criteria in the last 90 days.
- Veterans taking mood stabilizers and antipsychotic medications for specific psychiatric disorders.
- Veterans with a history of allergy to zonisamide.
- Veterans already receiving CPT.
Data sourced from ClinicalTrials.gov (NCT01847469). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.