Abstract | AIM: METHODS: A total of 400 patients (aged 6-18 years) were randomized to receive either 30 mg, 60 mg or 90 mg EPs-7630 or placebo daily. Primary outcome criterion was the change in the Bronchitis Severity Score (BSS) from day 0 to day 7. RESULTS: After 7 days of treatment, the change in the BSS total score was significantly better in the 60 mg and 90 mg groups compared with placebo that of the without relevant differences between these two dosages. Especially 'coughing', 'sputum' and ' rales at auscultation' improved under EPs-7630. Onset of effect was faster, time of bed rest shorter and treatment outcome and satisfaction with treatment were rated better. Tolerability was comparable with placebo in all treatment groups. CONCLUSION:
EPs-7630 is effective in acute bronchitis outside the strict indication for antibiotics in 6-18 years old patients, with a dose of 60 mg or 90 mg daily offering the best benefit/risk ratio. EPs-7630 significantly reduces the severity of symptoms, leads to a more favourable course of the disease and a faster recovery from acute bronchitis compared with the placebo, and is well tolerated.
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Authors | W Kamin, V G Maydannik, F A Malek, M Kieser |
Journal | Acta paediatrica (Oslo, Norway : 1992)
(Acta Paediatr)
Vol. 99
Issue 4
Pg. 537-43
(Apr 2010)
ISSN: 1651-2227 [Electronic] Norway |
PMID | 20070280
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Acute Disease
- Adolescent
- Bronchitis
(drug therapy)
- Child
- Dose-Response Relationship, Drug
- Female
- Humans
- Male
- Pelargonium
(chemistry)
- Plant Extracts
(administration & dosage, adverse effects)
- Plant Roots
(chemistry)
- Severity of Illness Index
- Treatment Outcome
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