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A Pilot Study of Ultra Rapid Opioid Rotation and Titration of Oxymorphone

NCT00945919 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2009-07-24

No results posted yet for this study

Summary

This project will explore the safety and feasibility of performing a successful intravenous patient controlled analgesia (IV PCA) Oxymorphone titration and conversion to oral ER Oxymorphone (extended release or OPANA ER) in the outpatient setting.

Conditions

  • Chronic Nociceptive Pain
  • Neuropathic Pain
  • Non-cancer Pain

Interventions

DRUG

Oxymorphone ER

Rapid Opioid rotation/titration

Sponsors & Collaborators

Principal Investigators

  • Marco Pappagallo, MD · Icahn School of Medicine at Mount Sinai

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2010-12-31
Completion
2011-05-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00945919 on ClinicalTrials.gov