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Methadone and Ketamine for Neuropathic Pain Treatment

Primary Purpose

Neuropathic Pain

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Methadone
Ketamine
Methadone plus Ketamine
Sponsored by
Universidade Federal de Santa Maria
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuropathic Pain focused on measuring Neuropathic pain, Methadone, Ketamine, Multimodal analgesia

Eligibility Criteria

22 Years - 77 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients complaining of pain for more than 6 months with neuropathic pain poorly responsive to drugs used to treat neuropathic pain (i.e. opioid, non-opioid, anticonvulsants, antidepressants), who were 22 to 77 years old

Exclusion Criteria:

  • patients with a history of severe psychiatric disorder,
  • misuse of illegal drugs or
  • hepatic disease

Sites / Locations

  • University Hospital in Santa Maria

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Methadone

Ketamine

Methadone plus ketamine

Arm Description

Group treated with methadone solution.

Group treated with ketamine solution

Group treated with methadone plus ketamine solution

Outcomes

Primary Outcome Measures

The primary outcome was pain intensity as assessed by visual analogical scale (VAS) scores

Secondary Outcome Measures

The secondary outcomes were the presence of burning and/or shooting pain, allodynia and side effects.

Full Information

First Posted
August 22, 2014
Last Updated
September 5, 2014
Sponsor
Universidade Federal de Santa Maria
Collaborators
Santa Casa de Misericórdia de Belo Horizonte, Hospital de Clinicas de Porto Alegre
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1. Study Identification

Unique Protocol Identification Number
NCT02233452
Brief Title
Methadone and Ketamine for Neuropathic Pain Treatment
Official Title
Management of Neuropathic Chronic Pain With Methadone Combined With Ketamine: Randomized, Double Blind, Active-controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal de Santa Maria
Collaborators
Santa Casa de Misericórdia de Belo Horizonte, Hospital de Clinicas de Porto Alegre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Methadone and ketamine are effective for neuropathic pain management. However, the benefits of the association of both drugs are uncertain. Here, the investigators conducted a randomized, double-blind, in parallel, active controlled clinical trial to test the hypothesis that methadone combined ketamine (methadone/ketamine) is more effective than methadone or ketamine alone in reducing neuropathic pain.
Detailed Description
Either oral methadone or ketamine have been used in neuropathic pain management, however, the benefits of the association of both drugs are uncertain. Here, we conducted a randomized, double-blind, in parallel, active controlled clinical trial to test the hypothesis that methadone combined ketamine (methadone/ketamine) is more effective than methadone or ketamine alone in reducing neuropathic pain. Methods: Fourthly two patients with neuropathic pain refractory to conventional therapy were randomly assigned to receive during three months oral methadone (n= 13), ketamine (n=13) or methadone combined with ketamine (n=13). The primary outcome was pain score on visual analogical scale (VAS) assessed on baseline, 8, 15, 30, 60 and 90 days throughout the treatment, and the secondary outcomes were symptoms of neuropathic pain such as allodynia, burning or shooting pain as well the side effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuropathic Pain
Keywords
Neuropathic pain, Methadone, Ketamine, Multimodal analgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
37 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methadone
Arm Type
Active Comparator
Arm Description
Group treated with methadone solution.
Arm Title
Ketamine
Arm Type
Active Comparator
Arm Description
Group treated with ketamine solution
Arm Title
Methadone plus ketamine
Arm Type
Active Comparator
Arm Description
Group treated with methadone plus ketamine solution
Intervention Type
Drug
Intervention Name(s)
Methadone
Other Intervention Name(s)
Methadone hydrochloride, Cristália® (São Paulo, Brazil)
Intervention Description
The solution of methadone was prepared by mixing 10 ml of methadone (10 mg/ml) and 90 ml of saline 0.9% (Baxter, São Paulo, Brazil)
Intervention Type
Drug
Intervention Name(s)
Ketamine
Other Intervention Name(s)
S(+)-ketamine hydrochloride, Cristália®, São Paulo, Brazil
Intervention Description
The solution of ketamine was prepared by mixing 20 ml of S(+)-ketamine hydrochloride (50 mg/ml, Cristália®, São Paulo, Brazil) and 80 ml of saline 0.9% (Baxter, São Paulo, Brazil), obtaining a concentration of 10 mg/ml of ketamine.
Intervention Type
Drug
Intervention Name(s)
Methadone plus Ketamine
Other Intervention Name(s)
methadone and S(+)-ketamine, Cristália®, São Paulo, Brazil
Intervention Description
the solution of methadone, ketamine was prepared by mixing 10 ml of methadone hydrochloride (10 mg/ml, Cristália®, São Paulo, Brazil), 20 ml of S(+)-ketamine hydrochloride (50 mg/ml, Cristália®, São Paulo, Brazil) and 70 ml of saline 0.9% (Baxter, São Paulo, Brazil), obtaining a concentration of 1 mg/ml of methadone and 10 mg/ml of ketamine.
Primary Outcome Measure Information:
Title
The primary outcome was pain intensity as assessed by visual analogical scale (VAS) scores
Time Frame
90 days
Secondary Outcome Measure Information:
Title
The secondary outcomes were the presence of burning and/or shooting pain, allodynia and side effects.
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
22 Years
Maximum Age & Unit of Time
77 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients complaining of pain for more than 6 months with neuropathic pain poorly responsive to drugs used to treat neuropathic pain (i.e. opioid, non-opioid, anticonvulsants, antidepressants), who were 22 to 77 years old Exclusion Criteria: patients with a history of severe psychiatric disorder, misuse of illegal drugs or hepatic disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juliano Ferreira, PhD
Organizational Affiliation
Federal University of Santa Catarina
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital in Santa Maria
City
Santa Maria
State/Province
Rio Grande do Sul
ZIP/Postal Code
97105-900
Country
Brazil

12. IPD Sharing Statement

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Methadone and Ketamine for Neuropathic Pain Treatment

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