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effect of aripiperazole in treatment of psychotic mania

COMPARISION THE EFFICACY OF ADJUCTIVE THERAPY RISPERIDON OR ARIPIPERAZOL TO LITIUM IN BIPOLAR DISORDER(MANIC PHAZE WITH PSYCHTIC FEATHER)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201409176691N2
Enrollment
60
Registered
2015-01-27
Start date
2014-04-21
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

Condition 1: mania. Condition 2: bipolar disorder. bipolar affective disorder bipolar affective disorder

Interventions

Intervention 1: Litium combined with Tabiet Aripiprazole(30 mg/day) as intervention group for 3 weeks. Intervention 2: Litium combined with Tablets Risperidon(6mg/day) as control group for 3weeks.
Treatment - Drugs
Litium combined with Tabiet Aripiprazole(30 mg/day) as intervention group for 3 weeks.
Litium combined with Tablets Risperidon(6mg/day) as control group for 3weeks.

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: criteria: Age more than 18 years; Diagnosis of Bipolar disorder with psychotic symptom based on DSM-IV TR; Ongoing treatment with Litium as a mood stabilazor with seromic level between 0.8-1.2meq/L ; patient with YMRA>20.Exclusion criteria: Mental Retardation; Pregnancy or Breast Inclusion feeding;Any chronic medical problem; substance abuse; Any other psychiatric Disorder in Axis I OR II;Allergic to Aripiprazole and other Atypical Antipsychotic drug ;History of epileptic disorder; Delirium state.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of manic phase and psychotic symptom. Timepoint: Baseline and days 7-14-21 after beginig of treatment. Method of measurement: YMRS.

Secondary

MeasureTime frame
Akatezia. Timepoint: days 2-4-7-10 after beginig of treatment then every weeks. Method of measurement: BARS.;Extrapyramidal. Timepoint: days 2-4-7-10 after beginig of treatment then every weeks. Method of measurement: AIMS.;Diskinesia. Timepoint: days 2-4-7-10 after beginig of treatment then every weeks. Method of measurement: SAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Fatemeh Sheikhmoonesi

Mazandaran University of Medical Sciences

fmoonesi@mazums.ac.ir+98 11 3326 1245

Outcome results

None listed

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