Switching From Morphine to Methadone. A Clinical, Pharmacological and Pharmacogenetic Study

NCT ID: NCT00184496

Last Updated: 2014-02-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-08-31

Study Completion Date

2009-09-30

Brief Summary

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Cancer patients on morphine for chronic pain, with side effects or unsatisfactory pain relief, will be rotated to Methadone. We will try to find out what is the best methode to rotate, and the equivalent dosage.

Detailed Description

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This study is based on the clinical observation that patients who are not well controlled on morphine or oxycodone may benefit from switching to another opioid, in this case methadone. Although the mechanism for such switch is not completely understood, evidence indicates that opioids with different chemical structures have different characteristics, not least in relation to new knowledge about genetic variation in opioid receptors. Another challenge is that there is much uncertainty regarding equianalgesic dose ratios for morphine and methadone. It seems that the higher the morphine doses, the relatively lower methadone doses are needed to substitute morphine. Furthermore, there is uncertainty to which switching procedures one should use, the most common ones are "stop and go" and a three days switch. Finally, it is reported that methadone may increase the QT interval of the ECG, and thus increase the risk for the ventricular arrhythmia Torsade de pointe. The aim of this randomized, open label, multicenter study is primarily to compare the switching procedures, but it will also provide more knowledge about equianalgesic dose ratios, the effect of methadone on the QT interval, genetical factors that may characterize patients needing opioid switch as well as their response to it, and finally if pharmacokinetic factors plays a role.

Conditions

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Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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methadon

Morphine methadone stop and go switch

Group Type ACTIVE_COMPARATOR

Methadone

Intervention Type DRUG

To methods for switching morphine to methadon. Stop-and go versus overlap

Methadone

Methadon morphine overlap switch

Group Type ACTIVE_COMPARATOR

Methadone

Intervention Type DRUG

To methods for switching morphine to methadon. Stop-and go versus overlap

Interventions

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Methadone

To methods for switching morphine to methadon. Stop-and go versus overlap

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* • Malignant disease.

* On morphine and in need of opioid rotation. (A patient in need of opioid rotation is defined as having insufficient pain control with or without unacceptable side effects from opioids).
* Able to complete the planned assessment schedules.
* Above 18 years of age.
* If out-patient, the patient lives with someone who can observe him/her.
* Given informed consent according to the ethical guidelines.

Exclusion Criteria

* Not able to read or write in Norwegian
* The patient has participated in a clinical study 4 weeks prior to inclusion
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Norwegian University of Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stein Kaasa, MD,PhD Prof.

Role: PRINCIPAL_INVESTIGATOR

St Olavs University Hospital, Trondheim

Locations

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St Olavs Hospital

Trondheim, Trondheim, Norway

Site Status

Countries

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Norway

References

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Moksnes K, Dale O, Rosland JH, Paulsen O, Klepstad P, Kaasa S. How to switch from morphine or oxycodone to methadone in cancer patients? a randomised clinical phase II trial. Eur J Cancer. 2011 Nov;47(16):2463-70. doi: 10.1016/j.ejca.2011.06.047. Epub 2011 Jul 19.

Reference Type RESULT
PMID: 21775131 (View on PubMed)

Other Identifiers

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OPI 03/008

Identifier Type: -

Identifier Source: org_study_id

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