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Effect of crocin supplementation in treatment of methadone maintenance treatment patients

The effect of crocin supplementation on cognitive functions, craving and withdrawal syndrome in methadone maintenance treatment patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170420033551N6
Enrollment
60
Registered
2019-07-09
Start date
2019-05-19
Completion date
Unknown
Last updated
2020-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Addiction. Other psychoactive substance related disorders

Interventions

Intervention 1: Intervention group: tablet of crocin, 15 mg, two oral tablet for 12 weeks. Intervention 2: Control group: placebo tablet, two oral tablet for 12 weeks.

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients on methadone maintenance treatment Age of 18 to 70 years old Evaluated by the drug abuse section of the Structured Clinical Interview for DSM-IV Seeking for treatment

Exclusion criteria

Exclusion criteria: Unwillingness to cooperate Current severe depression and mania Psychosis Consumption of crocin, antioxidant, and anti-inflammatory supplements during the last 3 months High blood pressure Hypothyroidism or hyperthyroidism

Design outcomes

Primary

MeasureTime frame
Craving. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Desire for Drug Questionnaire (DDQ craving).;Withdrawal syndrome. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Clinical opiate withdrawal symptoms (COWS).

Secondary

MeasureTime frame
Evaluation of cognitive function. Timepoint: At the baseline and after intervention (12 weeks). Method of measurement: Cognitive function questionnaire.;Verba Fluency. Timepoint: At the baseline and after intervention (12 weeks). Method of measurement: FAS task.;Speed Processing. Timepoint: At the baseline and after intervention (12 weeks). Method of measurement: Digit Symbol and Trial Making Test (TMT).;Memory. Timepoint: At the baseline and after intervention (12 weeks). Method of measurement: Wechsler intelligence Scale (DGSP).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Ghaderi

Kashan University of Medical Sciences

gaderiam@yahoo.com+98 31 5554 0021

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026