Citicoline in the treatment of acute ischaemic stroke: an international, randomised, multicentre, placebo-controlled study (ICTUS trial)
✍ Scribed by Antoni Dávalos; José Alvarez-Sabín; José Castillo; Exuperio Díez-Tejedor; Jose Ferro; Eduardo Martínez-Vila; Joaquín Serena; Tomás Segura; Vitor T Cruz; Jaime Masjuan; Erik Cobo; Julio J Secades
- Book ID
- 117310380
- Publisher
- The Lancet
- Year
- 2012
- Tongue
- English
- Weight
- 383 KB
- Volume
- 380
- Category
- Article
- ISSN
- 0140-6736
No coin nor oath required. For personal study only.
✦ Synopsis
Background Citicoline is approved in some countries for the treatment of acute ischaemic stroke. The drug has shown some evidence of effi cacy in a pooled analysis. We sought to confi rm the effi cacy of citicoline in a larger trial.
Methods
We undertook a randomised, placebo-controlled, sequential trial in patients with moderate-to-severe acute ischaemic stroke admitted at university hospitals in Germany, Portugal, and Spain. Using a centralised minimisation process, patients were randomly assigned in a 1:1 ratio to receive citicoline or placebo within 24 h after the onset of symptoms (1000 mg every 12 h intravenously during the fi rst 3 days and orally thereafter for a total of 6 weeks [2×500 mg oral tablets given every 12 h]). All study participants were masked. The primary outcome was recovery at 90 days measured by a global test combining three measures of success: National Institutes of Health Stroke Scale ≤1, modifi ed Rankin score ≤1, and Barthel Index ≥95. Safety endpoints included symptomatic intracranial haemorrhage in patients treated with recombinant tissue plasminogen activator, neurological deterioration, and mortality. This trial is registered, NCT00331890. Results 2298 patients were enrolled into the study from Nov 26, 2006, to Oct 27, 2011. 37 centres in Spain, 11 in Portugal, and 11 in Germany recruited patients. Of the 2298 patients who gave informed consent and underwent randomisation, 1148 were assigned to citicoline and 1150 to placebo. The trial was stopped for futility at the third interim analysis on the basis of complete data from 2078 patients. The fi nal randomised analysis was based on data for 2298 patients: 1148 in citicoline group and 1150 in placebo group. Global recovery was similar in both groups (odds ratio 1•03, 95% CI 0•86-1•25; p=0•364). No signifi cant diff erences were reported in the safety variables nor in the rate of adverse events.
Interpretation Under the circumstances of the ICTUS trial, citicoline is not effi cacious in the treatment of moderateto-severe acute ischaemic stroke.
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