Skip to content

The Effect of oxytocin on clinical signs, ACTH & cortisol levels and methamphetamine craving in matrix maintenance treatment

The Effect of oxytocin on clinical signs, ACTH & cortisol levels and methamphetamine craving in matrix maintenance treatment

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171129037673N1
Enrollment
50
Registered
2018-01-29
Start date
2017-12-22
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

Drug abuse. Drug abuse counseling and surveillance

Interventions

Intervention 1: Intervention group: Participants will receive oxytocin nasal spray, 10IU/spray, twice a day until 28 days. (One dose in each nostril (40IU daily)). Intervention 2: Control group: One t
Treatment - Drugs
Placebo
Intervention group: Participants will receive oxytocin nasal spray, 10IU/spray, twice a day until 28 days. (One dose in each nostril (40IU daily))
Control group: One time 40 IU intranasal saline

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 18-65 years old Male Methamphetamine dependency as assessed by the substance abuse section of the Structured Clinical Interview of DSM-IV Being at the Matrix Model of treatment. Seeking treatment for methamphetamine use Patients willing to participate in the intervention

Exclusion criteria

Exclusion criteria: Suicide attempts within the past 12 months; suicidal ideas or psychotic symptoms in the past 6 months determined by a study team physician Current opioid, alcohol or sedative physical dependence or cocaine dependence Major cardiovascular disorder Abnormal liver function Having severe psychotic disorders Metabolic diseases such as diabetes Neurological diseases Positive urine tests indicating abuse of any substance or stimulant Unwillingness to participate in the study

Design outcomes

Primary

MeasureTime frame
Measure of desire for methamphetamine. Timepoint: Complete questionnaire weekly. Method of measurement: CCQ-Brief Questionnaire.;Depression beck score. Timepoint: Complete questionnaire weekly. Method of measurement: Questionnaire.;Anxiety beck score. Timepoint: Complete questionnaire weekly. Method of measurement: Questionnaire.;ACTH level in the blood plasma. Timepoint: Before, middle and end of study. Method of measurement: Blood screening.;Cortisol level in the blood plasma. Timepoint: Before, middle and end of study. Method of measurement: Blood screening.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Azadbakht

Kashan University of Medical Sciences

azadbakht-a@mail.kaums.ac.ir+98 31 3338 1066

Outcome results

None listed

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