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Completed

NCT Number: NCT00067535

Assessment of Potential Interactions Between Cocaine and RPR 102681 - 1

The purpose of this study is to assess Potential Interactions Between iv Cocaine and RPR 102681

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Uniformed Services University of Health Science

Bethesda, Maryland, 20814 4799, United States

About this study

Phase I, Double-Blind, Placebo-Controlled Dose Escalating Assessment of Potential Interactions Between Intravenous Cocaine and RPR 102681

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Includes but is not limited to:

  • Non-treatment seekers
  • DSM-IV criteria for cocaine abuse or dependence
  • Ability to verbalize understanding of consent form and provide written informed consent and verbalize willingness to complete study procedures; be able to comply with protocol requirements

Exclusion criteria

Please contact site for more information.

Treatment and study plan

Cocaine-Related Disorders

Drug

Primary outcomes

  1. Hemodynamic response to cocaine and subjective response to cocaine

    Time frame: 3x / 30 days

Sponsors and collaborators

Lead sponsor

National Institute on Drug Abuse (NIDA)

Nih

Registry information

Official study title

Potential Interactions Between IV Cocaine and RPR 102681

Important dates

Study start
2003
Primary completion
2005
Study completion
2005
First posted
Aug 25, 2003
Registry last updated
Jan 12, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.