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Clinical Trial of Topiramate for Cocaine Addiction

Clinical Trial of Topiramate for Cocaine Addiction

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00685178
Enrollment
250
Registered
2008-05-28
Start date
2007-02-28
Completion date
2011-09-30
Last updated
2017-07-11

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

Conditions

Cocaine Dependence

Keywords

addiction, drug dependence, stimulant

Brief summary

This is an outpatient clinical trial of topiramate for addressing cocaine dependence and reduction of cocaine associated behaviors in opiate dependent drug users maintained on methadone treatment. The study aims to answer whether topiramate 1. is safe and acceptable to methadone patients 2. reduces cocaine use 3. helps with collateral problems such as alcohol abuse, tobacco dependence, anxiety, PTSD and/or pain symptoms. The study will also evaluate topiramate effect on neuro-cognitive performance.

Detailed description

This is an outpatient clinical trial of topiramate treatment for cocaine dependence and reduction of cocaine-associated HIV risk behavior. Topiramate is of high current interest in this regard, having been identified my National Institute on Drud Abuse (NIDA) leadership as among only a small number of tested candidates providing a positive signal and warranting further clinical investigation (Vocci, 2005). Topiramate is a marketed antiepileptic that enhances the GABAergic system and antagonizes the glutamatergic system, both new targets in the search for anti-cocaine treatments. A published pilot trial has supported topiramate's efficacy, and it is especially intriguing as potentially beneficial against other disorders prevalent among drug users, such as mood, anxiety, panic disorders, PTSD, pain and cognitive dysfunction, that may contribute to drug use. Design/Methods: This is phase II, double-blind randomized (stratified) 4 group, 2x2 design, evaluating topiramate versus placebo under each of two levels of cocaine-abstinence motivation -- cocaine-abstinence-contingent versus non-contingent voucher incentives. Conduct will be in a methadone maintenance context to ensure adequate retention and adherence, with participants dually dependent on opioids and cocaine. The target topiramate stabilization dose is 300 mg/day (150 mg b.i.d.), with one dose per day being observed at the clinic. The voucher-incentive manipulation provides valuable information about the role of motivation in modulating medication effects; it also provides a positive control condition to document the sensitivity of the study methods for detecting therapeutic benefit. Enrollment will be 300 patients ( 240 completers, 60/group). Participation will be up to 33 weeks - Baseline/Placebo-Run-in (5 weeks), Randomized Medication Treatment (20 weeks, induction, stable dosing, taper), Randomized Voucher Treatment (12 weeks, embedded in Medication period), and Therapeutic Disposition (up to 8 weeks). Data analysis focuses on the 8-week period of stable dosing and concurrent vouchers. The primary outcome variable is days abstinent from cocaine, as determined by a combination of self-report and objective confirmation by quantitative urinalysis toxicology of cocaine metabolite levels and application of the Preston rule for determining abstinence. Secondary outcome variables are measures of adverse behaviors and symptoms commonly co-occurring in cocaine abusers (alcohol abuse, tobacco use, depression, anxiety, PTSD, pain, neuro-cognitive and psychomotor performance dysfunction) that may contribute to drug use and/or detrimental effects. Significance: This randomized controlled clinical trial will provide valuable information about the actions and therapeutic effectiveness of the promising candidate anti-cocaine pharmacotherapy topiramate, and about the conditions, correlates, and modulators of any observed effectiveness. It will also provide valuable methodological information contributing to the continuing evolution of clinical trial methods for evaluating potential drug abuse treatment medications.

Interventions

DRUGtopiramate

topiramate powder 0mg - 150 mg with lactate in blind capsules. Two capsules dispensed daily. One capsule ingested under supervision at the methadone window. One capsule to be ingested at home at bedtime. Participant is expected to return the empty blister pack on the following day. capsules are administered from week 4 through 25 of the trial

monetary reward for self-reported cocaine abstinence confirmed by urine toxicology results

DRUGplacebo + NonCR

participant receives placebo capsules and monetary reinforcers by chance, irrespective of cocaine use or abstinence

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* 18 - 55 years old * active opioid and cocaine dependence * seeking treatment for cocaine and opioid dependence * eligible for methadone maintenance per state and federal regulations * able and willing to provide a urine sample thrice a week * willing to answer questionnaires on a weekly basis * willing to provide breath samples for presence of alcohol thrice weekly * fluent in the English language

Exclusion criteria

* allergy to sulfonamide drugs * diabetes, respiratory insufficiency, renal tubular acidosis, renal insufficiency, heart failure, liver insufficiency, chronic diarrhea, other chronic diseases predisposing to a risk of acidosis * history of nephrolithiasis * HIV positive individuals who meet AIDS criteria by CDC criteria or are taking antiretroviral medications * serious psychiatric illness (psychosis, dementia) * glaucoma or family history of glaucoma * prostate hyperplasia, shy bladder, irritable bladder, difficulty providing urine samples on demand * female participants: being pregnant, lactating, or unwilling to use an effective method of contraception * use of antiepileptic agents * benzodiazepine dependence * latex allergy

Design outcomes

Primary

MeasureTime frameDescription
Proportion of Cocaine Positive Urine Samples Per Treatment ConditionUrine samples collected 3 times weekly from week 1 through 26Percentage of cocaine positive urine samples as measured by Preston new use rule (50% reduction in cocaine metabolites from previous urine)

Secondary

MeasureTime frameDescription
Voucher Earnings12 weeks (Weeks 8-20)Voucher earnings used as a measurement of contigency management (CM) or operate conditioning. Volunteers were rewarded vouchers of escalating monetary value for cocaine abstinence, as indicated by a cocaine negative urine sample. The first cocaine negative urine earned a $2.50 voucher, and the value increased by $1.50 for each subsequent cocaine negative sample. Volunteers were awarded a bonus of $10.00 for every three consecutive cocaine negative urine samples. Urine samples were collected 3 times per week, and vouchers were attainable between Weeks 8 and 20. Contingency management as a measurement of operant conditioning in which positive reinforcement is applied (in this case vouchers of monetary value) and cocaine abstinence

Countries

United States

Participant flow

Pre-assignment details

250 volunteers were consented and admitted into the study; however 171 were randomized into the study. 79 volunteers were excluded due to a variety of reasons including failure to attend, adverse events (not study related), incarceration, failure to comply with study procedures, insufficient cocaine positive urines, and pregnancy

Participants by arm

ArmCount
1 Topiramate + CR
topiramate and contingency reinforcement for urine sample confirming cocaine abstinence topiramate: topiramate powder 0mg - 150 mg with lactate in blind capsules. Two capsules dispensed daily. One capsule ingested under supervision at the methadone window. One capsule to be ingested at home at bedtime. Participant is expected to return the empty blister pack on the following day. capsules are administered from week 4 through 25 of the trial Contingency Reinforcement: monetary reward for self-reported cocaine abstinence confirmed by urine toxicology results
40
2 Topiramate + NonCR
Topiramate and random reinforcement irrespective of cocaine use topiramate: topiramate powder 0mg - 150 mg with lactate in blind capsules. Two capsules dispensed daily. One capsule ingested under supervision at the methadone window. One capsule to be ingested at home at bedtime. Participant is expected to return the empty blister pack on the following day. capsules are administered from week 4 through 25 of the trial
45
4 Placebo + NonCR
placebo + NonCR: participant receives placebo capsules and monetary reinforcers by chance, irrespective of cocaine use or abstinence
39
3 Placebo + CR
Placebo and contingency reinforcement for urine sample confirming cocaine abstinence Contingency Reinforcement: monetary reward for self-reported cocaine abstinence confirmed by urine toxicology results
47
Total171

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003
Overall Studyadministrative (disciplinary) discharge0102
Overall StudyAdverse Event1524
Overall Studyincarcerated1370
Overall Studymissed 3 consecutive methadone clin days7526
Overall StudyPregnancy0001
Overall Studyvoluntary study discharge4511

Baseline characteristics

Characteristic2 Topiramate + NonCR4 Placebo + NonCR1 Topiramate + CR3 Placebo + CRTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
45 Participants39 Participants40 Participants47 Participants171 Participants
Age, Continuous41 years
STANDARD_DEVIATION 7
40 years
STANDARD_DEVIATION 8
43 years
STANDARD_DEVIATION 7
42 years
STANDARD_DEVIATION 7
42 years
STANDARD_DEVIATION 7
Region of Enrollment
United States
45 participants39 participants40 participants47 participants171 participants
Sex: Female, Male
Female
22 Participants19 Participants17 Participants24 Participants82 Participants
Sex: Female, Male
Male
23 Participants20 Participants23 Participants23 Participants89 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 400 / 450 / 390 / 47
other
Total, other adverse events
1 / 405 / 453 / 393 / 47
serious
Total, serious adverse events
4 / 404 / 451 / 393 / 47

Outcome results

Primary

Proportion of Cocaine Positive Urine Samples Per Treatment Condition

Percentage of cocaine positive urine samples as measured by Preston new use rule (50% reduction in cocaine metabolites from previous urine)

Time frame: Urine samples collected 3 times weekly from week 1 through 26

Population: This study utilized an Intent-to-Treat (ITT) analysis. The ITT analysis includes all volunteers who signed informed consent, were randomized into the study's treatment conditions, and took at least 1 dose of study medication.

ArmMeasureValue (NUMBER)
1 Topiramate + CRProportion of Cocaine Positive Urine Samples Per Treatment Condition45.4 percentage of positive urine samples
2 Topiramate + NonCRProportion of Cocaine Positive Urine Samples Per Treatment Condition42.7 percentage of positive urine samples
3 Placebo + CRProportion of Cocaine Positive Urine Samples Per Treatment Condition53.5 percentage of positive urine samples
4 Placebo + NonCRProportion of Cocaine Positive Urine Samples Per Treatment Condition46.5 percentage of positive urine samples
p-value: 0.531Chi-squared
Secondary

Voucher Earnings

Voucher earnings used as a measurement of contigency management (CM) or operate conditioning. Volunteers were rewarded vouchers of escalating monetary value for cocaine abstinence, as indicated by a cocaine negative urine sample. The first cocaine negative urine earned a $2.50 voucher, and the value increased by $1.50 for each subsequent cocaine negative sample. Volunteers were awarded a bonus of $10.00 for every three consecutive cocaine negative urine samples. Urine samples were collected 3 times per week, and vouchers were attainable between Weeks 8 and 20. Contingency management as a measurement of operant conditioning in which positive reinforcement is applied (in this case vouchers of monetary value) and cocaine abstinence

Time frame: 12 weeks (Weeks 8-20)

ArmMeasureValue (MEAN)Dispersion
1 Topiramate + CRVoucher Earnings421.25 DollarsStandard Error 79.58
2 Topiramate + NonCRVoucher Earnings343.26 DollarsStandard Error 65.34
3 Placebo + CRVoucher Earnings394.69 DollarsStandard Error 72.06
4 Placebo + NonCRVoucher Earnings203.51 DollarsStandard Error 50.89
Comparison: Analyses were performed to measure the correlation between CR groups (topiramate + CR and Placebo + CR) and abstinence.p-value: <0.001ANOVA
Comparison: Analyses were performed to measure the correlation between Non-CR groups (topiramate + NonCR and Placebo + NonCR) and abstinence.p-value: <0.001Generalized Estimating Equation (GEE)

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