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Assessing the effectiveness of treatment by aripiprazole and placebo for control of obsesion in patients with Bipolar mood disorder

Assessing the effectiveness of treatment by aripiprazole and placebo with lithium and benzodiazepin to control of obsesion in patients with Bipolar mood disorder

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014092719295N1
Enrollment
40
Registered
2017-03-07
Start date
2016-05-14
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: Bipolar disorder. Condition 2: Obsessive-Compulsive disorder. Bipolar affective disorder Obsessive-compulsive disorder

Interventions

Intervention 1: The study is a double blind clinical trial. Interventional Group (Group A) is 20 people that receive Aripiprazole in addition to Lithium and Benzodiazepine (if necessary). Administra
Treatment - Drugs
The study is a double blind clinical trial. Interventional Group (Group A) is 20 people that receive Aripiprazole in addition to Lithium and Benzodiazepine (if necessary). Administrator is doing Obs
This study is a double blind clinical trial. Control Group (Group B) is 20 people that receive Placebo in addition to Lithium and Benzodiazepine (if necessary). Administrator is doing obsession seve

Sponsors

Vice chancellery for Research Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with a diagnosis of bipolar disorder according to the DSM IV TR criteria; Yale Brown Score more than 16 at baseline; No important medical condition Exclusion criteria: Patients were not in acute phase of depression and mania; Important medical condition (cardiovascular, Respirator, renal, Gastrointestinal disease); Pregnancy; Yale Brown Score less than 16 at baseline

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Obsession severity. Timepoint: Weeks 0 and 4 and 8. Method of measurement: Yale Brown Test (Y-BOCS).

Secondary

MeasureTime frame
Side edffect. Timepoint: Weeks 4 and 8. Method of measurement: Side effect list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Ehsaei

Department of Psychiatry, Siraz University of Medical Sciences

Zahraehsaei@yahoo.com+98 71 3627 9319

Outcome results

None listed

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