WHO ICTRP trial
Pilot study on therapeutic efficacy of modafinil in idiopathic hypersomnie
EUCTR2008-007033-41-DE · EU Clinical Trials Register · Authorised
Key facts
| Trial ID | EUCTR2008-007033-41-DE |
|---|---|
| Public title | Pilot study on therapeutic efficacy of modafinil in idiopathic hypersomnie |
| Scientific title | Pilot study on therapeutic efficacy of modafinil in idiopathic hypersomnie |
| Primary sponsor | Hephata-Klinik |
| Registry | EU Clinical Trials Register |
| Recruitment status | Authorised |
| Study type | Interventional clinical trial of medicinal product |
| Countries | Germany |
| Conditions | To test the efficacy, tolerability and safety of modafinil for the treatment of of excessiv daytime sleepiness in patients with idiopathic hypersomnia without long sleep time. |
| Interventions | Trade Name: Vigil Product Name: Vigil Product Code: 34134.00.00 Pharmaceutical Form: Tablet Concentration unit: mg milligram(s) INN or Proposed INN: Modafinil Concentration unit: mg milligram(s) Concentration type: equal Concentration… |
| Registration date | Jan 29, 2009 |
| Secondary IDs | 1200 |
| Registry page | clinicaltrialsregister.eu |
At a glance
- No Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: