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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01907594
Other study ID # 6769
Secondary ID
Status Withdrawn
Phase Phase 2
First received
Last updated
Start date August 2013
Est. completion date September 2016

Study information

Verified date October 2020
Source New York State Psychiatric Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators previously developed a cigarette cue extinction treatment (CET) procedure in non-treatment seeking volunteer smokers in our nicotine laboratory. The goal of Cue Extinction Treatment is to un-pair a behavioral or autonomic response from the stimulus that triggers it. This is accomplished through repeated exposure to that trigger, while removing the patient's ability to act out the conditioned response. In the present study, the trigger is a lit cigarette, and the response the investigators seek to un-pair is cigarette craving. In the procedure the investigators have previously developed and intend to use again, the participant is shown a pack of his brand of choice cigarettes. The researcher removes a cigarette from the pack, lights it, and asks the participant to hold the cigarette without smoking it for 90 seconds. This procedure is repeated seven times over the course of a six-hour lab session. The investigators hope to boost the clinical response to smoking cue exposure therapy in quitters on NRT (nicotine replacement therapy) pretreatment by pharmacological augmentation with the partial NMDA receptor agonist D-cycloserine (DCS). Behavioral extinction training is a form of learning that may be modulated by NMDA receptor mediated glutamate transmission. The study's main hypothesis is that the partial NMDA receptor agonist D-cycloserine (DCS) facilitates cue exposure training and may prevent relapse to smoking. The aim of the proposed study is to assess whether DCS-facilitation of cue-exposure therapy improves abstinence among smokers on the nicotine patch seeking treatment. Development of an effective treatment strategy to enhance the effectiveness of NRTs would have a direct and significant positive impact on public health.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 2016
Est. primary completion date May 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 55 Years
Eligibility Inclusion Criteria:

1. Seeking treatment for nicotine dependence

2. Medically healthy on the basis of physical examination and medical history, vital signs, EKG, and laboratory tests, with a negative pregnancy test for females.

3. A DSM-IV diagnosis of nicotine dependence with physiological dependence. Has smoked at least 15 cigarettes daily for at least two years.

4. Able to perform study procedures.

5. Males or females between the ages of 21-55 yrs.

6. Female Participants agree to use an effective method of birth control

Exclusion Criteria:

1. A DSM-IV diagnosis of lifetime history of abuse or dependence on alcohol or drugs other than nicotine

2. Current Axis I diagnosis or current treatment with psychotropic medications (within last three months).

3. Lifetime history of schizophrenia or other psychotic disorders, bipolar disorder, or anxiety disorders.

4. Participants on parole or probation

5. History of significant recent violent behavior, e.g., one or more incidents of violent behavior in the past year resulting in physical damage.

6. Unstable medical condition, Blood pressure > 140/90, Pregnancy.

7. History of allergic reaction to nicotine patch.

8. History of hypersensitivity to cycloserine.

9. Any history of seizures

10. History of renal disease.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
D-cycloserine

Nicotine Replacement Therapy (patch)

Behavioral:
Smoking Cue Exposure

Progressive Muscle Relaxation

Drug:
Placebo
The investigators will administer Gelatin Capsule instead of D-Cycloserine in a double blind fashion to some of study subjects.

Locations

Country Name City State
United States New York State Psychiatric Institute New York New York

Sponsors (1)

Lead Sponsor Collaborator
New York State Psychiatric Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Cigarettes Smoked Smoking Diary kept of daily cigarette smoking. 3 months
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