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Comparing Opium Tincture (OT) With Methadone for Medication-assisted Treatment of Opioid Use Disorder (OT-RCT)

Primary Purpose

Opioid Dependence

Status
Completed
Phase
Phase 3
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
opium
methadone
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid Dependence focused on measuring Opium tincture, opium, methadone, opioid dependence, opiate dependence, clinical trial, Iran

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Opioid dependence as confirmed by DSM V diagnostic criteria
  • Willingness and ability to adhere to study protocol and follow-up schedule as determined through the pre-randomization period
  • Provide written informed consent.
  • Females of childbearing capacity must agree to use an acceptable method of birth control approved by the study investigator throughout the study.

Exclusion Criteria:

  • Active participant in another treatment program for opioid dependence within 14 days before inclusion in the study
  • Severe hepatic impairment (decompensated liver disease), a contraindication for methadone and its potential to precipitate hepatic encephalopathy.
  • Hypersensitivity to methadone syrup or other ingredients in the formulation
  • Pregnancy
  • Severe chronic respiratory disease
  • Head injury and raised intracranial pressure: Respiratory depressant effects (with CO2 retention and secondary elevation of CSF pressure) may be markedly exaggerated in the presence of head injury, or a preexisting increase in intracranial pressure. May produce effects that obscure the clinical course in participants with head injuries.
  • Biliary tract disease: may cause constriction of sphincter of Oddi.
  • Monoamine oxidase inhibitors use within 14 days of the study

Sites / Locations

  • Dodange Substance use disorder treatment center
  • Kian substance use treatment center
  • Tavalodi Digar
  • Rooz-e-No substance use treatment center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Opium

methadone

Arm Description

patient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population

patient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population

Outcomes

Primary Outcome Measures

Retention in treatment
percent of participants retained in the treatment

Secondary Outcome Measures

Craving
Visual analogue scale (0-10 scale)
Withdrawal symptoms
Subjective Opioid Withdrawal Scale (SOWS) Questionnaire
Physical health
Opiate Treatment Index (OTI)-Health section Questionnaire
Mental health
Symptom Checklist-90-Revised (SCL90-R) Questionnaire
Cognitive function
Montreal Cognitive Assessment (MOCA) Questionnaire
Severity of substance use problem
Addiction Severity Index-5th (ASI-5th) Questionnaire
Quality of life score from World Health Organization Quality of Life-BREF Questionnaire
World Health Organization Quality of Life-BREF (WHOQoL-BREF) Questionnaire
Client Satisfaction
Treatment Perception Questionnaire (TPQ)
Abstinence
Use of illicit opioids: Self-report / Use of amphetamines, methamphetamines, benzodiazepines: Self-report AND urine toxicology
Adverse events
Spontaneous reports AND checklist included in the Case Report Form (CRF), physical examination and lab data
Cost-effectiveness
Cost per Quality-adjusted life-month (QALM) and Quality-adjusted life-year (QALY) is calculated using Substance Abuse Services Cost Analysis Program (SASCAP).

Full Information

First Posted
July 13, 2015
Last Updated
July 10, 2019
Sponsor
University of British Columbia
Collaborators
Tehran University of Medical Sciences, Iran National Science Foundation, AJA University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02502175
Brief Title
Comparing Opium Tincture (OT) With Methadone for Medication-assisted Treatment of Opioid Use Disorder
Acronym
OT-RCT
Official Title
Comparing Opium Tincture (OT) and Methadone for Medication-assisted Treatment of Opioid Use Disorder: A Randomized Double-blind Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
June 22, 2017 (Actual)
Primary Completion Date
March 8, 2018 (Actual)
Study Completion Date
March 8, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia
Collaborators
Tehran University of Medical Sciences, Iran National Science Foundation, AJA University of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients with opioid use disorder seeking medication-assisted treatment will be recruited. Each participant will be allocated to one of the two study groups with the equal chance of receiving either opium tincture (OT) or methadone. Participants, clinical and research staff will not be aware of the medication that each patient receives. This study aims to test whether OT is as equally effective as methadone at retaining participants with opioid use disorder in medication-assisted treatment.
Detailed Description
Purpose: To compare the efficacy and safety of opium tincture (OT) with methadone syrup for medication-assisted treatment of individuals with opioid use disorder. Justification: Currently, methadone is the gold standard for medication-assisted treatment of opioid use disorder. Opium tincture could be a potential alternative treatment for this condition, and a promising solution to address the following issues: Alternative treatment option As no single treatment is effective for all individuals with opioid use disorder, sufficiently diverse treatment options should be available. Currently, treatment options for opioid use disorder are not always effective. Avoidance of overdose with methadone: The long-acting nature of methadone, its narrow therapeutic window, its high potency and associated lack of standard conversion ratio from and to other drugs, could result in fatal overdose. In contrast, OT has a shorter half-life and lower potency compared to methadone, which can account for a lower incidence of fatal overdose, especially in patients at higher risk of overdose with currently prescribed medications. Thus, OT could be an added treatment option to currently available treatments such as Buprenorphine/ Naloxone for medication-assisted treatment of patients with higher risk of overdose. Prolonged QT syndrome of methadone: Medication-assisted treatment with methadone can cause serious, potentially fatal adverse effects on the cardiac electrical conduction system leading to a prolonged QT interval and predisposing patients to arrhythmias. As such, cardiac conduction co-morbidity is a (relative) contraindication for the use of methadone as a medication-assisted treatment. Thus, OT could be an added treatment option to current available treatments such as buprenorphine or levomethadone for medication-assisted treatment of patients with cardiac conduction defects. Opium dependence as the dominant pattern of substance use To date, studies on medication-assisted treatment of opioid use disorder have mostly been carried out on populations in which heroin is the predominant substance of use and there is comparatively fewer data on patients with opium use disorder. Opium tincture could be the treatment of choice in geographic areas with higher prevalence of dependence on opium as the predominant pattern of substance use, such as Iran and some other Asian countries. Traditional medicine and cultural acceptance: Being a traditional herbal remedy for pain, OT appears to be a more culturally acceptable alternative to methadone in some parts of Southeast Asia. Cost-effectiveness: Possible cost effectiveness of OT for treatment of opioid use disorder can make it a potential treatment of choice if its efficacy and safety profile could be demonstrated through this RCT. Research methods: Recruitment strategy: Following methods will be used to recruit participants: 1) Brochures and flyers will be distributed in community outreach, general and mental hospitals, NGO-run communities, colleges and universities, drop-in centers and specialized clinics for treatment of participants with HIV and hepatitis C 2) Posters (same content as a brochures and flyers) of the study will be stuck in the billboard of bus/subway, local stores, hospitals, NGO-run communities, colleges and universities, as well as any specialized health-care center for psychiatry or addiction treatments 3) there are NGO-run communities for treating patients with opioid use disorder in Sari, Isfahan, and Shiraz. Investigators will use the initial contact letter to recruit from new patients attending these communities for receiving treatment. Randomization and blinding: Randomized to methadone or OT treatment arms will be carried out in a 1:1 allocation ratio using stratified randomization block technique with block sizes of 2. Age and gender distribution of the population with opioid-dependence in Iran is the basis for stratification on sex (F/M ratio = 1/9) and age (younger than 30/ 30-49/ 50 and older ~ 1: 2: 2). The investigators, treatment team (except pharmacist), assessors, and patients will only be aware of the randomization code for each participant, but not the treatment allocation label or randomization tables. Methadone syrup is made similar to OT in terms of smell, color, and taste using an essence. Sample size: The sample size was calculated using a fixed margin (95%-95%) approach based on the FDA guidelines for non-inferiority clinical trials (Food and Drug Administration, 2016). For the active control effect, a pooled 95% CI for retention ratio of methadone to placebo of 4.44 [3.26, 6.04] was considered (Mattick et al., 2009). The lower bound i.e., 3.26 was considered as M1, with calculated treatment effect of 2.26. M2 equal to 1.25 (11% of M1) was chosen as a conservative non-inferiority margin. Retention rate for participants in medication-assisted treatment with methadone was assumed to be 77.7% at 3 months based on a comprehensive systematic review (Feelemyer et al., 2014). Based on formula by Zhong, 2009, and assuming a power of 90% and Type I error set at 5%, the total sample size was initially calculated to be 240 participants, 120 in each group. Due to financial constraints, recruitment was set to stop at 200 given that it still provides a power more than 80% (a sample size of 174 provides a power of 80%). Statistical analysis plan: Retention in treatment will be compared between two groups using confidence interval procedure. Secondary outcomes will be compared between two groups using appropriate regression methods.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Dependence
Keywords
Opium tincture, opium, methadone, opioid dependence, opiate dependence, clinical trial, Iran

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
204 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Opium
Arm Type
Experimental
Arm Description
patient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population
Arm Title
methadone
Arm Type
Active Comparator
Arm Description
patient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population
Intervention Type
Drug
Intervention Name(s)
opium
Other Intervention Name(s)
tincture of opium, laudanum, Opium tincture
Intervention Description
Opium tincture (10mg/ml), manufactured by Daroupakhsh.co, Tehran, Iran.
Intervention Type
Drug
Intervention Name(s)
methadone
Intervention Description
Methadone (5mg/ml), manufactured by Daroupakhsh.co, Tehran, Iran.
Primary Outcome Measure Information:
Title
Retention in treatment
Description
percent of participants retained in the treatment
Time Frame
three months
Secondary Outcome Measure Information:
Title
Craving
Description
Visual analogue scale (0-10 scale)
Time Frame
Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Title
Withdrawal symptoms
Description
Subjective Opioid Withdrawal Scale (SOWS) Questionnaire
Time Frame
Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Title
Physical health
Description
Opiate Treatment Index (OTI)-Health section Questionnaire
Time Frame
Baseline, month 1, 2 and 3
Title
Mental health
Description
Symptom Checklist-90-Revised (SCL90-R) Questionnaire
Time Frame
Baseline, month 1, 2 and 3
Title
Cognitive function
Description
Montreal Cognitive Assessment (MOCA) Questionnaire
Time Frame
Baseline, month 1, 2 and 3
Title
Severity of substance use problem
Description
Addiction Severity Index-5th (ASI-5th) Questionnaire
Time Frame
Baseline, month 1, 2 and 3
Title
Quality of life score from World Health Organization Quality of Life-BREF Questionnaire
Description
World Health Organization Quality of Life-BREF (WHOQoL-BREF) Questionnaire
Time Frame
Baseline, month 1, 2 and 3
Title
Client Satisfaction
Description
Treatment Perception Questionnaire (TPQ)
Time Frame
month 3
Title
Abstinence
Description
Use of illicit opioids: Self-report / Use of amphetamines, methamphetamines, benzodiazepines: Self-report AND urine toxicology
Time Frame
Baseline, month 1, 2 and 3
Title
Adverse events
Description
Spontaneous reports AND checklist included in the Case Report Form (CRF), physical examination and lab data
Time Frame
Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Title
Cost-effectiveness
Description
Cost per Quality-adjusted life-month (QALM) and Quality-adjusted life-year (QALY) is calculated using Substance Abuse Services Cost Analysis Program (SASCAP).
Time Frame
three months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Opioid dependence as confirmed by DSM V diagnostic criteria Willingness and ability to adhere to study protocol and follow-up schedule as determined through the pre-randomization period Provide written informed consent. Females of childbearing capacity must agree to use an acceptable method of birth control approved by the study investigator throughout the study. Exclusion Criteria: Active participant in another treatment program for opioid dependence within 14 days before inclusion in the study Severe hepatic impairment (decompensated liver disease), a contraindication for methadone and its potential to precipitate hepatic encephalopathy. Hypersensitivity to methadone syrup or other ingredients in the formulation Pregnancy Severe chronic respiratory disease Head injury and raised intracranial pressure: Respiratory depressant effects (with CO2 retention and secondary elevation of CSF pressure) may be markedly exaggerated in the presence of head injury, or a preexisting increase in intracranial pressure. May produce effects that obscure the clinical course in participants with head injuries. Biliary tract disease: may cause constriction of sphincter of Oddi. Monoamine oxidase inhibitors use within 14 days of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael R Kausz, MD, PhD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shahin Akhondzadeh, PhD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dodange Substance use disorder treatment center
City
Mohammadabad
State/Province
Mazandaran
Country
Iran, Islamic Republic of
Facility Name
Kian substance use treatment center
City
Sari
State/Province
Mazandaran
Country
Iran, Islamic Republic of
Facility Name
Tavalodi Digar
City
Isfahan
Country
Iran, Islamic Republic of
Facility Name
Rooz-e-No substance use treatment center
City
Shiraz
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
30714249
Citation
Nikoo M, Moazen-Zadeh E, Nikoo N, Javidanbardan S, Kazemi A, Choi F, Vogel M, Gholami A, Tavakoli S, Givaki R, Jazani M, Mohammadian F, Markazi Moghaddam N, Goudarzi N, Schutz C, Jang K, Akhondzadeh S, Krausz M. Comparing opium tincture and methadone for medication-assisted treatment of patients with opioid use disorder: Protocol for a multicenter parallel group noninferiority double-blind randomized controlled trial. Int J Methods Psychiatr Res. 2019 Mar;28(1):e1768. doi: 10.1002/mpr.1768. Epub 2019 Feb 4.
Results Reference
derived

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Comparing Opium Tincture (OT) With Methadone for Medication-assisted Treatment of Opioid Use Disorder

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