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Progesterone for the Treatment of Cocaine Dependence - 1

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Cocaine-Related Disorders
Cocaine Abuse

Treatments

Other: Placebo
Drug: Progesterone

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00218257
R01DA014573 (U.S. NIH Grant/Contract)
0205M23681
DPMC

Details and patient eligibility

About

Past research has demonstrated that cocaine dependent women experience less severe responses to cocaine during the luteal phase of the menstrual cycle, when estrogen and progesterone concentrations are high. The purpose of this study is to determine whether administered progesterone reduces subjective and physiological responses to cocaine in cocaine dependent individuals.

Full description

Changes in ovarian hormones across the menstrual cycle impact responses to cocaine in women. Studies have shown that cocaine's effects are dampened during the luteal phase of the menstrual cycle, when estrogen and progesterone concentrations are high, relative to the other phases of the cycle, when concentrations of these hormones are relatively low. The purpose of this study is to determine whether progesterone reduces subjective and physiological responses to cocaine in cocaine dependent individuals. In addition, this study will help to advance the possibility of hormonal progesterone and pharmacologically-related drugs as potential treatment components for cocaine abuse.

Participants will undergo two 4-day inpatient periods, totaling 8 days of treatment. For women, the inpatient periods will occur during two consecutive menstrual cycles; for men, these will occur during two consecutive months. On Day 1, participants will receive a first dose of either progesterone or placebo. On Day 2, participants will receive a second and third dose of study medication. Participants will also participate in an adaptation session, which will familiarize the participant with the smoking equipment that will be used the following day. On Day 3, participants will receive a fourth dose of medication 2 hours prior to a smoking lab session. Prior to beginning the smoking lab session, participants will be asked to rate their current cocaine craving, anxiety level, appetite, and premenstrual symptoms. Participants will then be given a sample of the cocaine dose for the given day. During the smoking lab session, participants will be asked additional cocaine craving questions at pre-determined intervals and will be given the option to trade in previously earned tokens for either money or a dose of cocaine. Following completion of the smoking lab session, participants will receive their fifth dose of medication.

Enrollment

96 patients

Sex

All

Ages

18 to 46 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Smoked at least 1 gram of cocaine each week for the 6 months prior to study entry
  • Agrees to use an adequate method of contraception for the duration of the study
  • If female, current regular menses

Exclusion criteria

  • Major psychiatric illnesses, including psychotic mood and anxiety disorders
  • Current dependence on alcohol or drugs other that cocaine or nicotine
  • History of major medical illnesses, including liver disease, abnormal vaginal bleeding, suspected or known breast cancer, thrombophlebitis, or other medical conditions
  • Current use of oral contraceptives or other types of hormonal contraceptives
  • Amenorrhea
  • Currently on parole or probation
  • Received treatment for chemical dependency within the 6 months prior to study entry
  • Known allergy to progesterone or peanuts

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

96 participants in 2 patient groups, including a placebo group

Progesterone
Active Comparator group
Description:
200mg progesterone twice daily
Treatment:
Drug: Progesterone
Placebo
Placebo Comparator group
Description:
Placebo twice daily
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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