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A comparative study of piracetam effect

Can Piracetam control breath-holding spells and the symptoms of disease in children? A double blind RCT

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201010054872N1
Enrollment
61
Registered
2010-12-09
Start date
2007-04-30
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

breath holding spell. Other and unspecified abnormalities of breathing

Interventions

Intervention 1: Intervention group: administration of piracetam in 6 mounth period with dose of 40/mg/kg/day. Intervention 2: contorol group: administration of placebo in 6 mounth period.
Treatment - Drugs
Placebo
Intervention group: administration of piracetam in 6 mounth period with dose of 40/mg/kg/day
contorol group: administration of placebo in 6 mounth period

Sponsors

Ardeabil University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 14 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1)Parental consent for participation in the plan 2) Normal EEG 3) absent of systematic disease 4) Normal growth and Development 5)History of breath- Holding spell and physical and neurological examination by pediatric neurologist. 6) No Electrolyte Abnormality (Hypoglycemia and Hypocalcaemia ) Exclusion criteria: 1) Children with history of convulsion 2) Children that received Anticonvulsant drugs. 3) Delayed neurotic development 4) all Children with heart diseases 5) all children with anemia 6) Side effects of priacetam including true dizziness, convulsion, extra pyramidal sings, lethargy, headache, sleepiness; gastrointestinal complication including nausea and vomiting, diarrhea, constipation, anorexia, increased weight

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Interval time between BHS. Timepoint: before prevention and every 2 month in 6 month. Method of measurement: questionnaire & exam.;BHS duration. Timepoint: before prevention and every 2 month in 6 month. Method of measurement: Filling a questionnarie by asking questions from parents & exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mehrdad Mirzarahimi

Ardebil University of Medical Sciences

mirzarahimim@yahoo.com+98 914 452 6802

Outcome results

None listed

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