Opioid DependencePhase 3OT-RCTNCT02502175
Comparing Opium Tincture (OT) With Methadone for Medication-assisted Treatment of Opioid Use Disorder
A Phase 3 study testing opium and methadone in people with Opioid Dependence, run by University of British Columbia at 4 sites in Iran.
Trial 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. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Opioid Dependence
- What is being tested?
- opium and methadone
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 204 participants
- Where
- 4 sitesIran
- Study dates
- 22 Jun 2017to 8 Mar 2018
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- 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.
Who cannot join
- 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
Trial locations and contacts
4 sites in 1 country.
Iran4 sites
Tavalodi Digar
Isfahan
Dodange Substance use disorder treatment center
Moḩammadābād, Mazandaran
Kian substance use treatment center
Sari, Mazandaran
Rooz-e-No substance use treatment center
Shiraz
About this study
Official title: Comparing Opium Tincture (OT) and Methadone for Medication-assisted Treatment of Opioid Use Disorder: A Randomized Double-blind Controlled Clinical Trial
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.
Read the 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.
- Conditions
- Opioid Dependence
- Being tested
- opium, methadone
- Keywords
- Opium tincture, opium, methadone, opioid dependence, opiate dependence, clinical trial, Iran
- Medical subject headings
- Opioid-Related Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
opiumDrug
Also called tincture of opium, laudanum, Opium tincture
Opium tincture (10mg/ml), manufactured by Daroupakhsh.co, Tehran, Iran.
methadoneDrug
Methadone (5mg/ml), manufactured by Daroupakhsh.co, Tehran, Iran.
| Study group | Role | What they receive |
|---|---|---|
| Opium | Experimental | patient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population Receives: Drug: opium |
| methadone | Active comparator | patient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population Receives: Drug: methadone |
What is being measured
The primary outcome is the main question the study is designed to answer.
Retention in treatment
percent of participants retained in the treatment
Measured: three months
Secondary outcomes (11)
Craving
Visual analogue scale (0-10 scale)
Measured: Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Withdrawal symptoms
Subjective Opioid Withdrawal Scale (SOWS) Questionnaire
Measured: Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Physical health
Opiate Treatment Index (OTI)-Health section Questionnaire
Measured: Baseline, month 1, 2 and 3
Mental health
Symptom Checklist-90-Revised (SCL90-R) Questionnaire
Measured: Baseline, month 1, 2 and 3
Cognitive function
Montreal Cognitive Assessment (MOCA) Questionnaire
Measured: Baseline, month 1, 2 and 3
Severity of substance use problem
Addiction Severity Index-5th (ASI-5th) Questionnaire
Measured: Baseline, month 1, 2 and 3
Quality of life score from World Health Organization Quality of Life-BREF Questionnaire
World Health Organization Quality of Life-BREF (WHOQoL-BREF) Questionnaire
Measured: Baseline, month 1, 2 and 3
Client Satisfaction
Treatment Perception Questionnaire (TPQ)
Measured: month 3
Abstinence
Use of illicit opioids: Self-report / Use of amphetamines, methamphetamines, benzodiazepines: Self-report AND urine toxicology
Measured: Baseline, month 1, 2 and 3
Adverse events
Spontaneous reports AND checklist included in the Case Report Form (CRF), physical examination and lab data
Measured: Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
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).
Measured: three months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2015 (estimated)
- Study start22 Jun 2017
- Primary completion8 Mar 2018
- Study completion8 Mar 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Opioid DependenceStudies of the same condition, open and under way.
- More trials run by University of British ColumbiaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 204 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of British Columbia
- Sponsor type
- University, hospital or other
- Collaborators
- Tehran University of Medical Sciences, Iran National Science Foundation, AJA University of Medical Sciences
- Responsible party
- Principal investigator, Michael Krausz, University of British Columbia
- Investigators
- Michael R Kausz, MD, PhD, Principal investigator, University of British ColumbiaShahin Akhondzadeh, PhD, Principal investigator, Tehran University of Medical Sciences
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02502175
- Sponsor's protocol ID
- H15-00220
- Acronym
- OT-RCT
- Status last verified
- Jul 2019
- First submitted
- 13 Jul 2015
- Last updated
- 12 Jul 2019
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Nikoo M, Kianpoor K, Nikoo N, Javidanbardan S, Kazemi A, Choi F, Vogel M, Gholami A, Tavakoli S, Wong JSH, Moazen-Zadeh E, Givaki R, Jazani M, Mohammadian F, Moghaddam NM, Schutz C, Jang K, Akhondzadeh S, Krausz M. Opium tincture versus methadone for opioid agonist treatment: a randomized controlled trial. Addiction. 2023 Feb;118(2):284-294. doi: 10.1111/add.16030. Epub 2022 Sep 7.
PubMed 35971297Nikoo 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.
PubMed 30714249
Study at a glance
From the registry record, last updated by the sponsor on 12 Jul 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparing Opium Tincture (OT) and Methadone for Medication-assisted Treatment of Opioid Use Disorder: A Randomized Double-blind Controlled Clinical Trial
- ClinicalTrials.gov ID
- NCT02502175
- Acronym / sponsor ID
- OT-RCT / H15-00220
- Conditions
- Opioid Dependence
- Keywords
- Opium tincture, opium, methadone, opioid dependence, opiate dependence, clinical trial, Iran
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 204 participants (actual)
- Lead sponsor
- University of British ColumbiaUniversity, hospital or other
- Collaborators
- Tehran University of Medical Sciences, Iran National Science Foundation, AJA University of Medical Sciences
- Study start
- 22 Jun 2017 (actual)
- Primary completion
- 8 Mar 2018 (actual)
- Study completion
- 8 Mar 2018 (actual)
- First posted
- 20 Jul 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Opium | Experimental | Drug: opiumpatient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population |
| methadone | Active comparator | Drug: methadonepatient-centered flexible dosing in line with the national protocol published by Iranian Ministry of Health for maintenance treatment of opioid dependent population |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (4 listed)
- 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.
Key exclusion criteria (8 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| opiumAlso: tincture of opium, laudanum, Opium tinctureOpium tincture (10mg/ml), manufactured by Daroupakhsh.co, Tehran, Iran. | Drug | Opium |
| methadoneMethadone (5mg/ml), manufactured by Daroupakhsh.co, Tehran, Iran. | Drug | methadone |
Primary outcome
Retention in treatment
Time frame: three months
percent of participants retained in the treatment
11 secondary outcomes
Craving
Time frame: Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Withdrawal symptoms
Time frame: Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Physical health
Time frame: Baseline, month 1, 2 and 3
Mental health
Time frame: Baseline, month 1, 2 and 3
Cognitive function
Time frame: Baseline, month 1, 2 and 3
Severity of substance use problem
Time frame: Baseline, month 1, 2 and 3
Quality of life score from World Health Organization Quality of Life-BREF Questionnaire
Time frame: Baseline, month 1, 2 and 3
Client Satisfaction
Time frame: month 3
Abstinence
Time frame: Baseline, month 1, 2 and 3
Adverse events
Time frame: Day 1-3/ Twice daily | Day 4-14/ Once daily | Day 15-28/ Three times a week | Day 29-84/ Once weekly
Cost-effectiveness
Time frame: three months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Jul 2019.
- Derived from this study: PubMed 35971297Nikoo M, Kianpoor K, Nikoo N, Javidanbardan S, Kazemi A, Choi F, Vogel M, Gholami A, Tavakoli S, Wong JSH, Moazen-Zadeh E, Givaki R, Jazani M, Mohammadian F, Moghaddam NM, Schutz C, Jang K, Akhondzadeh S, Krausz M. Opium tincture versus methadone for opioid agonist treatment: a randomized controlled trial. Addiction. 2023 Feb;118(2):284-294. doi: 10.1111/add.16030. Epub 2022 Sep 7.
- Derived from this study: PubMed 30714249Nikoo 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Michael R Kausz, MD, PhD principal investigator
University of British Columbia
Shahin Akhondzadeh, PhD principal investigator
Tehran University of Medical Sciences
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing opium and methadone in people with Opioid Dependence, run by University of British Columbia at 4 sites in Iran.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 12 Jul 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in Iran. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Retention in treatment (time frame: three months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02502175, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jul 2019.