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ECG changes and C-protein level variations during and after treatment with atorvastatin at different dosages in the secondary prevention of stroke. - ND

ECG changes and C-protein level variations during and after treatment with atorvastatin at different dosages in the secondary prevention of stroke. - ND

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-010761-22-IT
Enrollment
Unknown
Registered
2009-02-23
Start date
2009-04-25
Completion date
Unknown
Last updated
2014-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke MedDRA version: 9.1 Level: LLT Classification code 10055221 Term: Ischemic stroke

Interventions

Trade Name: TORVAST Pharmaceutical Form: Tablet INN or Proposed INN: Atorvastatin Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 20-

Sponsors

POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age ranging from 18 and 90 years; -Ischemic cerebral stroke with a neurologic syndrome related to a partial or complete infarct of posterior and/or anterior cerebral vascularization territory, following Bamford criteria. Included patients have to present one of the following clinical presentations: 1. at least one fo the following neurological deficits (depending to just one hemisphere impairment): 1.a. dysphasia or dyscalculia (for the impairment of the dominant hemisphere), visuo-spatial defict (i.e. neglect) for the impairment of the non-dominant hemisphere; 1.b. motor or sensory deficit involving at least two somatic districts, including face, arm and leg in the same side. 1.c. Homonymous hemianopsia or quadrantanopsia. 2. isolated superior function cerebral deficit. 3. motor or sensory deficit involving one arm or the face and the hand of the affected side. 4. vertebro-basilar syndrome. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: hemorrhagic stroke -Neurological deficit due to other causes instead of ischemia. -participation in another research protocol. -Blood, autoimmune or inflammatory cerebral diseases. -impossibility to partecipate to follow-up clinical controls.

Design outcomes

Primary

MeasureTime frame
Main Objective: Effects of the atorvastatine in the prognosis and in the frequency of new strokes during the follow-up period.;Secondary Objective: ND;Primary end point(s): ND

Countries

Italy

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026