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Celecoxib and Autism

A double-blind placebo controlled trial of celecoxib added to risperidone in patients with autistic disorder.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138711091556N2
Enrollment
40
Registered
2009-02-12
Start date
2009-02-19
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

Autism. Childhood autism

Interventions

Intervention 1: Intervention: Risperidone + Celecoxib 300 mg/day. Intervention 2: Control: Risperidone + placebo.
Treatment - Drugs
Placebo
Intervention: Risperidone + Celecoxib 300 mg/day

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 11 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Ages 3 to 11 years, clinical diagnosis of autism (the diagnosis of autism based on semi structured interview with the parent), lack of use of psychotropic drugs at least two weeks before trial. Exclusion Criteria: Previously received neuroleptics or any psychotropic drug treatment 6 months prior to recruitment or having significant active medical problem; Children with severe or profound mental retardation in whom a definitive diagnosis of autism could not be made; Any diagnosis of psychiatric disorder in Axis I and II; Any organic disorder.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The Aberrant Behavior Checklist (ABC). Timepoint: every two weeks. Method of measurement: The Aberrant Behavior Checklist (ABC).;Childhood Autism Rating Scale. Timepoint: every two weeks. Method of measurement: Childhood Autism Rating Scale.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 26, 2026