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A Comparison of the Addiction Liability of Hydrocodone and Sustained Release Morphine

CompletedPhase 4NCT00314340
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Characterize the relative abuse liability of a short versus a long acting opioid in chronic pain patients.

Study details

Official title
A CTSC Clinical Research Center Study: A Comparison of the Addiction Liability of Hydrocodone and Sustained Release Morphine
Conditions
Interventions
  • Behavioral: Markers of Abuse Liability, Neuropsych Testing, and Cue Reactivity
  • Drug: ER Morphine
  • Drug: hydrocodone plus acetaminophen
  • Drug: placebo
Sponsor
University of California, Davis
Start date
2005-11
Primary completion
2008-04
Sex
All
Age range
from 18 Years to 70 Years
Healthy volunteers
true
Results posted
Yes, on ClinicalTrials.gov
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients with chronic pain for periods greater than 6 months * Patients taking greater than 80 mg morphine equivalents of a short acting opioid (\>8 vicodin or 4 oxycodone/day) * Referral to Pain or Substance Abuse Clinic for self-escalation of opioids Exclusion Criteria: * Inability to understand and comprehend spoken English * Patients with Munchausen's syndrome * Patient has a history of Peripheral Vascular Disease * Patient has a history of Raynaud's Phenomenon * Liver Disease; Child's classification greater than 1 (liver cirrhosis) will be excluded * Renal disease (BUN \>25 or Cr \>1.5) * Congestive Heart Failure; Subjects with New York Heart Association (NYHA)Heart Failure Symptom Classification System Level of Impairment II, III and IV will be excluded * Coronary artery disease; recent MI within the past six months or recent history of angina not controlled with NTG within the past six months * Hypertension; 1)previously normotensive subject; systolic bp \>140 mm Hg and diastolic bp \> 90 mm Hg 2) Hx of active treatment with antihypertensive medications; systolic bp \>150 mm Hg and diastolic bp \> 100 mm Hg * Cerebrovascular disease; recent history within the past year of a transient ischemic attack or recent history within the past year of a cerebrovascular event * Malignancy requiring active treatment * Patient is pregnant (as ascertained by a self-report and a mandatory commercial pregnancy test before any study medication is consumed)

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00314340