search
Back to results

Tramadol to Reduce Opioid Withdrawal Symptoms

Primary Purpose

Opioid-Related Disorders

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Tramadol
Naloxone
Morphine
Sponsored by
National Institute on Drug Abuse (NIDA)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid-Related Disorders focused on measuring Opiate Addiction, Opiate Dependence

Eligibility Criteria

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

Inclusion Criteria: Meets DSM-IV diagnostic criteria for opioid dependence Is in good physical health Qualifies for treatment with opioid agonist therapy (e.g., methadone) If female, must have a negative pregnancy test prior to study entry Exclusion Criteria: Evidence of significant medical illness (e.g., insulin dependent diabetes mellitus) Evidence of significant psychiatric illness (e.g., schizophrenia) Currently seeking treatment for substance abuse Pregnant or breastfeeding

Sites / Locations

  • Johns Hopkins University (BPRU) Bayview Campus

Outcomes

Primary Outcome Measures

Opioid withdrawal symptoms (measured by Visual Analog Scale during the experimental sessions)
Opioid agonist effects (measured by Visual Analog Scale during the experimental sessions)
Physiological effects (measured by pulse oximeter, blood pressure, heart rate, and pupillary camera during the experimental sessions)

Secondary Outcome Measures

Full Information

First Posted
September 1, 2005
Last Updated
January 11, 2017
Sponsor
National Institute on Drug Abuse (NIDA)
search

1. Study Identification

Unique Protocol Identification Number
NCT00142896
Brief Title
Tramadol to Reduce Opioid Withdrawal Symptoms
Official Title
Withdrawal Suppression Efficacy of Tramadol
Study Type
Interventional

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
December 2005 (Actual)
Study Completion Date
December 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Drug Abuse (NIDA)

4. Oversight

5. Study Description

Brief Summary
Individuals with opioid addiction often experience serious withdrawal symptoms that may make relapse unavoidable. Tramadol, a medication that is currently used to treat pain caused by chronic conditions such as cancer or joint pain, may also be effective at reducing opioid withdrawal symptoms. This study will evaluate the effectiveness of tramadol at reducing withdrawal symptoms in individuals addicted to opioid drugs.
Detailed Description
Opioid withdrawal symptoms are a major contributing factor for why opioid treatment programs often fail. Individuals with severe opioid withdrawal symptoms may experience shaking, muscle and bone pain, nausea, depression, anxiety, and drug craving. Tramadol is a medication that is currently used to treat moderate to severe pain in individuals with cancer, joint pain, or pain resulting from surgery. Because of its pharmacological profile, tramadol may also be useful in treating opioid withdrawal. Further research is needed to confirm the benefits of tramadol for opioid addicts. The purpose of this study is to evaluate the effectiveness of tramadol at reducing opioid withdrawal symptoms in opioid-dependent individuals. This 6-week inpatient study will enroll opioid-dependent individuals. Participants will be required to reside at the research clinic for the entire study. All participants will receive morphine maintenance treatment on a daily basis. Twice a week participants will take part in experimental challenge sessions in which they will be randomly assigned to receive varying doses of tramadol, naloxone, morphine, or placebo. These sessions will assess the ability of tramadol to suppress opioid withdrawal symptoms. Participants will complete performance tasks to measure psychomotor and cognitive functioning. Heart rate and blood pressure will be monitored throughout the experimental sessions. A specialized camera will also be used to assess pupillary response of the eyes. Questionnaires and self-reports will be completed to assess medication effects and withdrawal symptoms. Following the end of the study, all participants will be offered outpatient drug abuse treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid-Related Disorders
Keywords
Opiate Addiction, Opiate Dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Tramadol
Intervention Type
Drug
Intervention Name(s)
Naloxone
Intervention Type
Drug
Intervention Name(s)
Morphine
Primary Outcome Measure Information:
Title
Opioid withdrawal symptoms (measured by Visual Analog Scale during the experimental sessions)
Title
Opioid agonist effects (measured by Visual Analog Scale during the experimental sessions)
Title
Physiological effects (measured by pulse oximeter, blood pressure, heart rate, and pupillary camera during the experimental sessions)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV diagnostic criteria for opioid dependence Is in good physical health Qualifies for treatment with opioid agonist therapy (e.g., methadone) If female, must have a negative pregnancy test prior to study entry Exclusion Criteria: Evidence of significant medical illness (e.g., insulin dependent diabetes mellitus) Evidence of significant psychiatric illness (e.g., schizophrenia) Currently seeking treatment for substance abuse Pregnant or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric C. Strain, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University (BPRU) Bayview Campus
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224-6823
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Tramadol to Reduce Opioid Withdrawal Symptoms

We'll reach out to this number within 24 hrs