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Evaluating the Effectiveness of Memantine on the Symptoms of Acute Mania in the Patients with Bipolar 1 Disorder

Evaluating the Effectiveness of Memantine as Adjuvant Treatment on the Symptoms of Acute Mania in the Patients with Bipolar 1 Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121725031N6
Enrollment
90
Registered
2017-01-30
Start date
2014-07-23
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

Bipolar I disorder. Bipolar affective disorder, current episode hypomanic

Interventions

Intervention 1: Placebo capsule, once a day will start at the baseline and after 3 days will increase to twice a day. In the sixth day, placebo dose will increase to 3 times a day and will continue wi
Placebo
Treatment - Drugs
Placebo capsule, once a day will start at the baseline and after 3 days will increase to twice a day. In the sixth day, placebo dose will increase to 3 times a day and will continue with same dose unt
Memantine 10 mg capsule, once a day will start at the baseline and after 3 days will increase to twice a day. In the sixth day, memantine dose will increase to 3 times a day and will continue with the

Sponsors

Vice Chancellor for Research of Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Between 18 to 60 years old; Meet the criteria for bipolar disorder based on DSM-1V-TR diagnostic criteria and clinical interview by a psychiatrist; Existence of mania, with a minimum score of 20 in Young Mania Rating Scale; Lack of psychiatric diseases; Without mental retardation; Lack of any disease that make a problem in the clinical study; Do not consume narcotic, stimulants and alcohol except nicotine in the three last months; Do not electroconvulsive therapy in the previous month; Not pregnant; Without drug allergy and drug side effects history on the this study drugs; Do not consume memantine in the three last months; Lack of dementia, delirium, cognitive disorders and epilepsy. Exclusion criteria: Drugs side effect that causing discontinuation of consume them; Request by the patient or the patient's parent or legal guardian to withdraw from the study at any time of the study; Consume of alcohol or narcotic by the patient after starting the study; Lack of response to the drug therapy after 2 weeks.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical symptoms of mania. Timepoint: At the beginning of treatment, second week, forth week and eighth week. Method of measurement: Young Mania Rating Scale Measure.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Alireza Rafiei

Amir Kabir Hospital

rafieidr93@gmail.com; rafiei90dr@yahoo.com; rafiei93dr@gmail.com+98 863313471519

Outcome results

None listed

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