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Celecoxib versus placebo as an adjunct in the treatment of Adolescents with bipolar mood disorder.

Celecoxib versus placebo as an adjunct in the treatment of Adolescents with bipolar mood disorder: a double blind randomized, placebo controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015080423478N1
Enrollment
40
Registered
2016-05-09
Start date
2016-04-03
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 disorder. Bipolar affective disorder, current episode manic without psychotic symptoms

Interventions

Intervention 1: Intervention group: All patients treated with lithium , and risperidone and celecoxib. The dose of celecoxib is 100 mg twice a day. Intervention 2: Control group: All patients treated
Treatment - Drugs
Placebo
Intervention group: All patients treated with lithium , and risperidone and celecoxib. The dose of celecoxib is 100 mg twice a day.
Control group: All patients treated with lithium , risperidone and placebo. All patients received a starting dose of risperidone combined with lithium 1 mg in all patients, and within 10 days of the f

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences, DR Masud Younesian
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Bipolar disorder (first episode); acute illness episode; manic phase; and Young Mania Rating Scale score 20 or more; age 12 to 18 years Exclusion criteria: Liver, kidney, heart and thyroid disorders at present; history of renal dysfunction or heart or a history of stomach ulcers; hypersensitivity to sulfonamides; co-morbidity risk of autism spectrum disorders; the risk of mental retardation; substance abuse over the past year; Mood Disorder caused by physical illness such as seizures; head trauma and other diseases

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bipolar disorder. Timepoint: Second week, Forth week, Week eight. Method of measurement: YMRS scale.

Secondary

MeasureTime frame
Patient function. Timepoint: Before treatment and at week eight. Method of measurement: CGAS Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyd Yaser Musavi

Tehran University of Medical Science

Yaser135778@yahoo.com+98 21 5542 1959

Outcome results

None listed

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