Skip to content

The Study of Hypiran effect on Methamphetamine associated psychosis patients

The Study of Hypiran (Hypericum Perforatum) effect on oxidative stress and neurotrophic factors in Methamphetamine associated psychosis patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016082129447N1
Enrollment
40
Registered
2016-10-31
Start date
2017-04-21
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

Methamphetamine associated psychosis. Mental and behavioural disorders due to use of hallucinogens

Interventions

Intervention 1: Hypiran medication will be prescribed in the intervention group. The dosage of hypiran use is 60 drops three times a day for one month. (60 drops of hypiran has 0.3 mg of the acti
Treatment - Drugs
Hypiran medication will be prescribed in the intervention group. The dosage of hypiran use is 60 drops three times a day for one month. (60 drops of hypiran has 0.3 mg of the active ingredient ca
Placebo will be prescribed in the control group. The dosage of placebo use is 60 drops three times a day for one month.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the patients who are current methamphetamine users have been admitted to the hospital; age between 18 and 70 years old; they have met the criteria for methamphetamine induced psychotic disorder according to DSM-5. Exclusion criteria: having a diagnosis of bipolar I and II disorder; substance induced mood disorder (with manic symptoms); liver and kidney diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Glutathione Peroxidase. Timepoint: before intervention, 14 and 28 days after intervention. Method of measurement: colorimetry.;Glutathione Reductase. Timepoint: before intervention, 14 and 28 days after intervention. Method of measurement: colorimetry.;Total Antioxidant Capacity. Timepoint: before intervention, 14 and 28 days after intervention. Method of measurement: colorimetry.;Nitric Oxide. Timepoint: before intervention, 14 and 28 days after intervention. Method of measurement: Elisa.;Malondialdehyde. Timepoint: before intervention, 14 and 28 days after intervention. Method of measurement: Elisa.;Selenoprotein1. Timepoint: before intervention, 14 and 28 days after intervention. Method of measurement: Elisa.;Methamphetamine. Timepoint: 14 after intervention. Method of measurement: HPLC.

Secondary

MeasureTime frame
BDNF. Timepoint: before intervetion and 28 days after intervention. Method of measurement: ELISA.;VEGF. Timepoint: before intervetion and 28 days after intervention. Method of measurement: ELISA.;DTNBP1. Timepoint: before intervetion and 28 days after intervention. Method of measurement: ELISA.;IL-6. Timepoint: before intervetion and 28 days after intervention. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mehrdad Eftekhar

Iran University of Medical Sciences

mehrdad.eftekhar@gmail.com+98 21 8670 3083

Outcome results

None listed

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