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The effectiveness of Rivastigmine on treatment of Tardive dyskinesia

The effectiveness of Rivastigmine on reducing the symptoms of Tardive dyskinesia in patients with Schizophrenia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012092910964N1
Enrollment
40
Registered
2013-01-08
Start date
2011-10-23
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

Tardive dyskinesia. Drug-induced dystonia

Interventions

Intervention 1: in intervention group: Rivastigmine,1.5 mg capsules, twice a day, in 4 weeks. Intervention 2: in control group: sugar,1.5 mg capsules, twice a day, in 4 weeks.
Treatment - Drugs
in intervention group: Rivastigmine,1.5 mg capsules, twice a day, in 4 weeks.
in control group: sugar,1.5 mg capsules, twice a day, in 4 weeks.

Sponsors

University of Social Welfare and Rehabilitation Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age range between 18 to 65 years, Spent at least one year of treatment with antipsychotics, to have a stable condition of the patient for at least one month prior to study entry. Exclusion criteria: Organic brain disease, Any neurological disorders, Having a chronic health problem, Change in the amount or type of antipsychotic medication or tranquilizers were used during the last 6 months so that might affect the patient's motor symptoms, Patients with mental retardation, Patients with thyroid disorders, Diabetes, and Substance Abusers.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Tardive dyskinesia symptoms. Timepoint: At baseline and after eight weeks follow-up. Method of measurement: Abnormal Involuntary Movement Scale (AIMS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Amirabbas Jahanian

University of Social Welfare and Rehabilitation

azadeh_yaraghchi@yahoo.com; Iran+98 21 2228 0765

Outcome results

None listed

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