Methamphetamine dependency. Mental and behavioural disorders due to use of other stimulants, including caffeine
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1. Ability to reading and writing in Persian; 2. Age between 18 and 55 years old; 3. All participants with diagnosis of methamphetamine dependency according to the DSM IV criteria; 4. Agreement to participating in study; Exclusion criteria: 1. Participants currently enrolled in another investigational device or drug trial or previously enrolled (within last 30 days) in investigative research of a device or pharmaceutical agent; 2. Co - use of methamphetamine and methadone; 3. Inability to tolerate buprenorphine; 4. Presence of any liver failure such as hepatitis; 5. History of any lung disease; 6. Presence of any thyroid disease such hypothyroidism or hyperthyroidism; 7. Presence of adrenal gland disease such as addison disease; 8. Presence of kidney failure such as CRF, ARF, etc. 9. Presence of heart failure; 10. Presence of prostatic hyperplasia or urethra tightness; 11. History of epilepsy or uncontrolled seizures; 12. Presence of any cancer; 13. Pregnancy; 14. Any evidences to confirm participants sail buprenorphine outside the addiction treatment center or any evidences to confirm participants will not use buprenorphine; 15. No acceptance to enroll in or continue the study;
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Existence of methamphetamine in urine samples. Timepoint: three times in a week in first three months, one time a week in second three months of following. Method of measurement: Urine rapid test kit (Methamphetamine). | — |
Secondary
| Measure | Time frame |
|---|---|
| Obsessive Compulsive Drug Use Scale (OCDUS) score. Timepoint: At the baseline and after that at 4th, 8th and 12th weeks after starting the intervention. Method of measurement: OCDUS questionnaire.;Remaining until end of study. Timepoint: after the end of the study. Method of measurement: observation of attending patient at the end of study.;Score on the Addiction Severity Index (ASI-Lite). Timepoint: At the baseline and after the end of the 12th week. Method of measurement: ASI-Lite questionnaire.;Score on the Leeds Dependence Questionnaire (LDQ). Timepoint: At the baseline and after that at 4th, 8th and 12th weeks after starting the intervention. Method of measurement: LDQ questionnaire.;Score on the WHO quality of life questionnaire (WHOQOL-BREF). Timepoint: At the baseline and after that at 4th, 8th and 12th weeks after starting the intervention. Method of measurement: WHOQOL-BREF questionnaire.;Added at 2015-04-03: Cognitive abilities. Timepoint: Added at 2015-04-03: At the baseline and after that at 4th, 8th, 12th and 24th weeks after starting the intervention. Method of measurement: Added at 2015-04-03: Cognitive Abilities Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences