WHO ICTRP trial
Assessment of bronchial hyperresponsiveness in children - inhalation of Mannitol…
EUCTR2007-003543-67-SE · EU Clinical Trials Register · Authorised
Key facts
| Trial ID | EUCTR2007-003543-67-SE |
|---|---|
| Public title | Assessment of bronchial hyperresponsiveness in children - inhalation of Mannitol compared to eucapnic voluntary hyperventilation and methacholine provocation |
| Scientific title | Assessment of bronchial hyperresponsiveness in children - inhalation of Mannitol compared to eucapnic voluntary hyperventilation and methacholine provocation |
| Primary sponsor | Karolinska Universitetssjukhuset |
| Registry | EU Clinical Trials Register |
| Recruitment status | Authorised |
| Study type | Interventional clinical trial of medicinal product |
| Countries | Sweden |
| Conditions | Three different methods to assess airway hyperresponsiveness in children with allergic asthma will be compared. |
| Interventions | Trade Name: Aridol Pharmaceutical Form: Inhalation powder, hard capsule INN or Proposed INN: Mannitol Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 0, 5, 10, 20, 40- Product Name: Methacholine… |
| Registration date | Sep 13, 2007 |
| Secondary IDs | 2007-285-31-3 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: