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Sublingual Methadone for the Management of Cancer Breakthrough Pain

This study has been completed.
Calgary Health Region
Information provided by:
AHS Cancer Control Alberta Identifier:
First received: July 29, 2005
Last updated: January 18, 2012
Last verified: August 2011
A dose titration protocol for sublingual methadone hydrochloride for the management of cancer-related breakthrough pain to find the optimal dose.

Condition Intervention Phase
Drug: Methadone
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Evaluation of a Dose Titration Protocol for Sublingual Methadone Hydrochloride for the Management of Cancer-related Breakthrough Pain

Resource links provided by NLM:

Further study details as provided by AHS Cancer Control Alberta:

Primary Outcome Measures:
  • Determine optimal dose titration
  • Determine assessment protocol

Estimated Enrollment: 10
Study Start Date: September 2003
Study Completion Date: January 2007
Primary Completion Date: June 2006 (Final data collection date for primary outcome measure)
Detailed Description:
This is a dose titration protocol for sublingual methadone hydrochloride for the management of cancer-related breakthrough pain to find the optimal dose.

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • > 18 years of age
  • Experiences episodes of breakthrough pain which respond to opioid therapy
  • Controlled baseline pain
  • Cognitive status sufficient for accurate completion of assessment form
  • Willing to provide written informed consent
  • Ability to hold a volume of 1 cc of water under the tongue for 5 minutes

Exclusion Criteria:

  • Currently or has received methadone during the previous week
  • Recent history of substance abuse
  • Severe respiratory impairment or other contraindications to opioids
  • Recently received therapies that had the potential to alter pain intensity or response to analgesics
  • Symptomatic anemia
  Contacts and Locations
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Please refer to this study by its identifier: NCT00125294

Sponsors and Collaborators
Alberta Health Services
Calgary Health Region
Principal Investigator: Neil Hagen Alberta Cancerboard
  More Information Identifier: NCT00125294     History of Changes
Other Study ID Numbers: 17208
Calgary Health Region
Study First Received: July 29, 2005
Last Updated: January 18, 2012

Keywords provided by AHS Cancer Control Alberta:
cancer pain
breakthrough pain
dose titration
sublingual route of administration
Cancer related pain
currently taking narcotics

Additional relevant MeSH terms:
Breakthrough Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Analgesics, Opioid
Central Nervous System Depressants
Physiological Effects of Drugs
Sensory System Agents
Peripheral Nervous System Agents
Antitussive Agents
Respiratory System Agents processed this record on May 22, 2017