Skip to content

Topiramate and Prolonged Exposure

Combining Topiramate and Prolonged Exposure for PTSD and Alcohol Use Disorder

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03176953
Acronym
TOP
Enrollment
100
Registered
2017-06-06
Start date
2017-11-01
Completion date
2023-09-30
Last updated
2023-11-18

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

Conditions

PTSD and Alcohol Use Disorder

Keywords

PTSD, alcohol use disorder, Veterans

Brief summary

Alcohol use disorder (AUD) and posttraumatic stress disorder (PTSD) frequently co-occur, and having both disorders is associated with greater psychological and functional impairment than having either disorder alone. The most effective PTSD treatment, prolonged exposure (PE) is sometimes less effective when individuals also have AUD. Anti-relapse medication appears promising to improve the effectiveness of PE to help individuals reduce alcohol use and PTSD symptoms and improve functioning. This study compares PE with and without topiramate, a medication shown to both reduce drinking and PTSD symptoms, with the hypothesis that combined PE and topiramate will be more effective than PE and placebo. The aim of this grant is to improve treatment outcomes for Veterans with AUD and PTSD.

Detailed description

Objectives. Alcohol use disorder (AUD) and posttraumatic stress disorder (PTSD) frequently co-occur, and having one condition worsens the course of the other. Individuals with both disorders exhibit worse functioning across a number of domains than individuals with either disorder alone. Prolonged exposure therapy (PE) is among the most effective treatments for PTSD. PE has been rated as a frontline treatment by multiple guidelines and reviews including the VA/DoD Clinical Practice Guidelines for the treatment of PTSD. However, in studies of individuals with PTSD and AUD, changes in alcohol use are only slightly better than in control or standard care conditions, reductions in PTSD symptoms are sometimes modest relative to studies of PE in PTSD patients without AUD, and rates of drop out from treatment are high. Combining PE with medication to curb drinking shows promise to improve upon the effectiveness of PE for individuals with comorbid AUD and PTSD, although thus far few studies have examined combining psychotherapy and medication. Topiramate is the single medication that has shown effectiveness for both AUD and PTSD and shows promise for reducing drinking among individuals with AUD and PTSD. However, the effect of adding topiramate to PE to treat comorbid AUD/PTSD has yet to be examined. The critical next step is to test a best practice PTSD treatment, PE, together with a promising pharmacological agent, topiramate, which has been found to be effective for both AUD and PTSD. Innovation: This application seeks to shift current clinical practice paradigms. A refinement to existing interventions is proposed through integration of two evidence based treatments. Methodology. The investigators propose to use a randomized, controlled, double blind study design to examine the effect of adding topiramate (TOP) to a best practice treatment for PTSD, PE. Participants will be 120 male and female Veterans from all services with AUD and PTSD. The investigators' primary aims are to determine the relative efficacy of PE+topiramate, as compared to PE+placebo, in reducing problematic drinking, reducing PTSD symptoms, and improving functioning and quality of life among Veterans with comorbid AUD/PTSD at post-treatment and 3- and 6-month post-treatment follow-up. The investigators will explore the extent to which decreases in drinking and PTSD symptoms lead to improvement in functioning. The proposed study has the potential to improve functional and psychological recovery for a highly prevalent and highly impaired population of Veterans. This study will test a novel and innovative combination of psychotherapy and medication with the goal of improving the care of Veterans. The successful completion of this project will help change the practices that drive treatment for Veterans who have both AUD and PTSD. The fundamental rationale for this study is to improve the evidence base that informs how patients with AUD and PTSD can attain sustained recovery from both of these disorders. The investigators will also explore whether changes in PTSD symptoms in the PE+TOP condition are partially explained by reductions in alcohol cravings.

Interventions

DRUGtopiramate

active medication

BEHAVIORALprolonged exposure

psychotherapy

DRUGplacebo

non-active medication

Sponsors

University of California, San Diego
CollaboratorOTHER
VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Double blind study. Only pharmacist will have access to randomization table.

Intervention model description

Participants randomly assigned to one of two conditions.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Veterans of the U.S. military and/or Reserve/National Guard members, 2. at least 18 years of age, 3. survivors of a psychological trauma meeting DSM-5 criterion A, and are at least one month post-trauma, 4. have current DSM-5 diagnoses of AUD and PTSD based on semi-structured diagnostic interviews, 5. have at least 20 days of heavy drinking (\>= 5 drinks/day for men and \>= 4/drinks per day for women) in the last 90 days spent in a non-restricted environment and meet criteria for heavy drinking at least 4 days in the last 30 days prior to screening, 6. are not currently receiving trauma-focused psychotherapy, 7. are literate in English and intend to stay in the San Diego area during the study, 8. are willing to attend psychotherapy, medication, and assessment sessions, 9. trying or planning to try to cut down on or abstain from alcohol, 10. for females of childbearing potential, agree to use an approved form of contraception for the duration of the study, including hormonal contraceptives (e.g., oral contraceptives or implantable devices), intrauterine device (IUD), or double barrier methods (e.g., diaphragm with spermicidal condom); barrier method is preferred as topiramate may make birth control less effective, 11. Individuals with clinically significant renal disease and/or impaired renal function, as defined by clinically significant elevation of blood urea nitrogen (BUN) or creatinine or an estimated creatinine clearance of \< 60 mL/min, can be included with physician approval, however the dosing schedule and maximum dose will be adjusted in accordance with FDA prescribing guidelines, 12. if individual is on another addiction medication, they should be on a stable approved addiction medication dose (at least two weeks before starting study drug) throughout the study, 13. are capable of giving informed consent.

Exclusion criteria

1. Subjects known to have clinically significant unstable medical or psychiatric conditions, where participation is deemed by investigators and study physicians to be risky, including but not limited to: * AST and/or ALT \>5 times the upper limit of the normal range and/or an increased serum bilirubin \>2 times the upper limit of normal. * Seizure disorders 2. have been treated with Topiramate for any reason in the past and discontinued the drug due to hypersensitivity reaction 3. in the opinion of the investigator, should not be enrolled because of the precautions, warnings, or contraindications listed on the Topiramate package insert, (e.g., certain types of glaucoma), 4. are pregnant, lactating, or plan to become pregnant during the period of participation in the study 5. in the judgment of the investigator, represent a significant risk of suicidal or homicidal behavior

Design outcomes

Primary

MeasureTime frameDescription
CAPS-5 ChangeChange from baseline to 16 weeksPTSD symptom diagnostic interview CAPS-5 score range = 0 - 80 Higher scores = more severe PTSD symptoms
Timeline Followback Interview (TLFB)Change from baseline to 16 weekssubstance use severity score range = 0 - 100% of heavy drinking days higher scores = greater percentage of total days that included heavy drinking

Countries

United States

Participant flow

Participants by arm

ArmCount
Prolonged Exposure + Topiramate
psychotherapy plus active medication topiramate: active medication prolonged exposure: psychotherapy
50
Prolonged Exposure + Placebo
psychotherapy plus placebo medication prolonged exposure: psychotherapy placebo: non-active medication
50
Total100

Baseline characteristics

CharacteristicProlonged Exposure + TopiramateTotalProlonged Exposure + Placebo
Age, Continuous45.86 years
STANDARD_DEVIATION 12.39
45.27 years
STANDARD_DEVIATION 12.6
44.67 years
STANDARD_DEVIATION 12.9
Education
College degree
15 Participants32 Participants17 Participants
Education
GED/High School Diploma
7 Participants14 Participants7 Participants
Education
Missing
5 Participants9 Participants4 Participants
Education
Some college
23 Participants45 Participants22 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
13 Participants30 Participants17 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
36 Participants68 Participants32 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
1 Participants2 Participants1 Participants
Race (NIH/OMB)
American Indian or Alaska Native
4 Participants4 Participants0 Participants
Race (NIH/OMB)
Asian
2 Participants3 Participants1 Participants
Race (NIH/OMB)
Black or African American
7 Participants22 Participants15 Participants
Race (NIH/OMB)
More than one race
3 Participants7 Participants4 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants1 Participants1 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants2 Participants1 Participants
Race (NIH/OMB)
White
33 Participants61 Participants28 Participants
Region of Enrollment
United States
50 Participants100 Participants50 Participants
Sex/Gender, Customized
sex
female
8 Participants16 Participants8 Participants
Sex/Gender, Customized
sex
male
42 Participants84 Participants42 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 500 / 50
other
Total, other adverse events
4 / 502 / 50
serious
Total, serious adverse events
3 / 502 / 50

Outcome results

Primary

CAPS-5 Change

PTSD symptom diagnostic interview CAPS-5 score range = 0 - 80 Higher scores = more severe PTSD symptoms

Time frame: Change from baseline to 16 weeks

Population: All randomized participants

ArmMeasureGroupValue (MEAN)Dispersion
Prolonged Exposure + TopiramateCAPS-5 Changebaseline CAPS36.720 score on a scaleStandard Error 1.794
Prolonged Exposure + TopiramateCAPS-5 Change16-week CAPS21.006 score on a scaleStandard Error 1.988
Prolonged Exposure + PlaceboCAPS-5 Changebaseline CAPS38.600 score on a scaleStandard Error 1.794
Prolonged Exposure + PlaceboCAPS-5 Change16-week CAPS29.872 score on a scaleStandard Error 2.016
Primary

Timeline Followback Interview (TLFB)

substance use severity score range = 0 - 100% of heavy drinking days higher scores = greater percentage of total days that included heavy drinking

Time frame: Change from baseline to 16 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Prolonged Exposure + TopiramateTimeline Followback Interview (TLFB)Baseline53.5 percentage of daysStandard Error 3.6
Prolonged Exposure + TopiramateTimeline Followback Interview (TLFB)16 week10.8 percentage of daysStandard Error 4.1
Prolonged Exposure + PlaceboTimeline Followback Interview (TLFB)Baseline52.1 percentage of daysStandard Error 3.6
Prolonged Exposure + PlaceboTimeline Followback Interview (TLFB)16 week16.2 percentage of daysStandard Error 4.2

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