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A double-blind trial comparing disodium cromoglycate (DSCG), and ketotifen in extrinsic asthmatic children
Insights
Disodium cromoglycate (DSCG) and ketotifen offer comparable symptom relief for extrinsic asthma in children. This 12-week trial found no significant side effects or changes in PEFR for either asthma medication.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Clinical Pharmacology
Background:
- Extrinsic asthma is a common chronic respiratory condition in children.
- Effective long-term management strategies are crucial for improving quality of life.
- Disodium cromoglycate (DSCG) and ketotifen are established treatments for asthma.
Purpose of the Study:
- To compare the efficacy and safety of disodium cromoglycate (DSCG) and ketotifen in children with extrinsic asthma.
- To evaluate symptom control and identify any adverse effects over a 12-week period.
Main Methods:
- A double-blind, non-crossover trial involving 27 children with extrinsic asthma.
- Assessment using symptom score and drug score charts over 12 weeks.
- Monitoring of weight, arterial pressure, pulse rate, and peak expiratory flow rate (PEFR).
Main Results:
- Both DSCG and ketotifen demonstrated similar protective effects against asthma symptoms.
- No participants withdrew due to adverse events; no side effects were observed in weight, blood pressure, or pulse.
- PEFR values remained stable for both treatment groups throughout the study.
- A non-significant trend for increased need for corticosteroid support was noted in the ketotifen group.
Conclusions:
- Disodium cromoglycate (DSCG) and ketotifen are equally effective and well-tolerated for managing extrinsic asthma in children.
- Both medications provide comparable symptom control without impacting PEFR or causing significant adverse effects.
- Further investigation may be warranted regarding the trend for additional corticosteroid support in the ketotifen group.
Abstract:
A double-blind non crossover trial comparing disodium cromoglycate (DSCG), with ketotifen, was carried out in twenty-seven extrinsic asthmatic children over 12 weeks. Assessment was made using symptom score and drug score charts. Both drugs showed a similar protective effect in the group studied. None of the subjects had to withdraw from the trial and no side-effects were noted in weight-curve, arterial pressure and pulse rate. PEFR values remained unchanged for both drugs throughout the trial. A non-significant tendency for additional corticosteroid support in the Ketotifen group was noted.