WHO ICTRP trial
High dose atorvastatin in acute ischemic stroke ? Monocenter pilot study - ADIS…
EUCTR2008-000433-21-IT · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2008-000433-21-IT |
|---|---|
| Public title | High dose atorvastatin in acute ischemic stroke ? Monocenter pilot study - ADIS 1.0 |
| Scientific title | High dose atorvastatin in acute ischemic stroke ? Monocenter pilot study - ADIS 1.0 |
| Primary sponsor | AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no |
| Countries | Italy |
| Conditions | acute ischemic stroke MedDRA version: 9.1 Level: LLT Classification code 10057613 Term: Thromboembolic stroke |
| Interventions | Trade Name: TORVAST*50CPR RIV 80MG PVC-AL Pharmaceutical Form: Coated tablet INN or Proposed INN: Atorvastatin Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 80- Pharmaceutical form of the placebo… |
| Registration date | Mar 17, 2008 |
| Target size | 150 |
| Secondary IDs | 14/2008/U/Sper |
| Registry page | clinicaltrialsregister.eu |
At a glance
- Yes Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: