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Clinical Trial of Topiramate for Cocaine Addiction

Primary Purpose

Cocaine Dependence

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
topiramate
Contingency Reinforcement
placebo + NonCR
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cocaine Dependence focused on measuring addiction, drug dependence, stimulant

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Behavioral Pharmacology Research Unit

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Placebo Comparator

Active Comparator

Arm Label

1 topiramate + CR

2 topiramate + NonCR

4 Placebo + NonCR

3 Placebo + CR

Arm Description

topiramate and contingency reinforcement for urine sample confirming cocaine abstinence

Topiramate and random reinforcement irrespective of cocaine use

Placebo and contingency reinforcement for urine sample confirming cocaine abstinence

Outcomes

Primary Outcome Measures

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)

Secondary Outcome Measures

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

Full Information

First Posted
May 23, 2008
Last Updated
June 9, 2017
Sponsor
Johns Hopkins University
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00685178
Brief Title
Clinical Trial of Topiramate for Cocaine Addiction
Official Title
Clinical Trial of Topiramate for Cocaine Addiction
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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 is safe and acceptable to methadone patients reduces cocaine use 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine Dependence
Keywords
addiction, drug dependence, stimulant

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
250 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 topiramate + CR
Arm Type
Experimental
Arm Description
topiramate and contingency reinforcement for urine sample confirming cocaine abstinence
Arm Title
2 topiramate + NonCR
Arm Type
Experimental
Arm Description
Topiramate and random reinforcement irrespective of cocaine use
Arm Title
4 Placebo + NonCR
Arm Type
Placebo Comparator
Arm Title
3 Placebo + CR
Arm Type
Active Comparator
Arm Description
Placebo and contingency reinforcement for urine sample confirming cocaine abstinence
Intervention Type
Drug
Intervention Name(s)
topiramate
Other Intervention Name(s)
topamax®, CAS 97240-79-4
Intervention Description
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
Intervention Type
Behavioral
Intervention Name(s)
Contingency Reinforcement
Other Intervention Name(s)
contingency management
Intervention Description
monetary reward for self-reported cocaine abstinence confirmed by urine toxicology results
Intervention Type
Drug
Intervention Name(s)
placebo + NonCR
Intervention Description
participant receives placebo capsules and monetary reinforcers by chance, irrespective of cocaine use or abstinence
Primary Outcome Measure Information:
Title
Proportion of Cocaine Positive Urine Samples Per Treatment Condition
Description
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
Secondary Outcome Measure Information:
Title
Voucher Earnings
Description
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)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Annie Umbricht, M.D.
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Behavioral Pharmacology Research Unit
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24814607
Citation
Umbricht A, DeFulio A, Winstanley EL, Tompkins DA, Peirce J, Mintzer MZ, Strain EC, Bigelow GE. Topiramate for cocaine dependence during methadone maintenance treatment: a randomized controlled trial. Drug Alcohol Depend. 2014 Jul 1;140:92-100. doi: 10.1016/j.drugalcdep.2014.03.033. Epub 2014 Apr 16.
Results Reference
derived
Links:
URL
http://dx.doi.org/10.1016/j.drugalcdep.2014.03.033
Description
Umbricht A∗, DeFulio A, Winstanley EL, Tompkins DA, Peirce J, Mintzer MZ, Strain EC, Bigelow GE (2014) Topiramate for cocaine dependence during methadone maintenance treatment: a randomized controlled trial Drug and Alcohol Dependence 140:92-100

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Clinical Trial of Topiramate for Cocaine Addiction

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