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Clinical Efficacy of Piracetam on the Treatment of Breath _Holding Spells

Clinical Efficacy of Piracetam on the Treatment of Breath _Holding Spells

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138801231808N1
Enrollment
50
Registered
2009-06-29
Start date
2009-04-15
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 spells. Other and unspecified abnormalities of breathing

Interventions

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

Sponsors

Mazandaran University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1) History of breath- Holding spell and physical and neurological examination by pediatric neurologist. 2) Minimum age 6 month and maximum 3 years old 3) Normal EEG 4) absent of systematic disease 5) Normal growth and Development 6) No history of epilepsy in family member 7) 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, sleepy; gastrointestinal complication including nausea and vomiting, diarrhea, constipation, anorexia, increased weight

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The number of Breath-holding spell. Timepoint: before prevention and 2 weeks after prevention. Method of measurement: questionarie of parents.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMotahareh kheradmand

Mazandaran Univercity of Medical sciences and Health ervices

elhamkheradmand2003@yahoo.comkheradmand@mazums.ac.ir+98 15132612458

Outcome results

None listed

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