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effect of habb-o-shefa in treatment of adiction

effect of habb-o-shefa in maintenance treatment of opiate dependent person

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015101024446N1
Enrollment
60
Registered
2015-11-16
Start date
2015-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

addiction. Mental and behavioural disorders due to use of opioids

Interventions

Intervention 1: Intervention group: habb-o-shefa capsule( 500 mg ) dose: 1 cap three time a day for 12 weeks( 3 month). Intervention 2: control group: sugar capsule( 500 mg ) dose: 1 cap three time a
Treatment - Drugs
Placebo
Intervention group: habb-o-shefa capsule( 500 mg ) dose: 1 cap three time a day for 12 weeks( 3 month)
control group: sugar capsule( 500 mg ) dose: 1 cap three time a day for 12 weeks( 3 month)

Sponsors

Vice Chancellor for research of Shahed University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 18 - 65 years old ; DSM-IV criteria for addiction ; healthy condition ; detoxification at least one month before intervention; signed informed consent Exclusion criteria: Addiction to alcohol ; positive history of other psychological disorders ; taking psychiatric drug ; pregnancy and breast feeding ; serious medical disease such as glaucoma ,retention ,epilepsy ,parkinsonism ; allergic reaction to medical herbs ; incidence of side effect

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Baseline, 4,8 and12 weeks after starting the medication. Method of measurement: Hamilton rating scale for anxiety.;Craving. Timepoint: Baseline, 4,8 and12 weeks after starting the medication. Method of measurement: Craving Beliefs Questionnaire.;Quality of life. Timepoint: Baseline, 4,8 and12 weeks after starting the medication. Method of measurement: wHO-QOL Brief.

Secondary

MeasureTime frame
Side effect. Timepoint: 4,8 and12 weeks after starting the medication. Method of measurement: physical examination and checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSayyed Abdalali Moosavyzadeh

Shahed University

alimoosavy@yahoo.com+98 21 2288 2521

Outcome results

None listed

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