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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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A collaborative, double-blind randomized study of cetiedil citrate in sickle cell crisis.

We have recently completed a double-blind, placebo-controlled, noncrossover study, the goal of which was to determine whether cetiedil citrate (cetiedil) could affect the course of vaso-occlusive crises in sickle cell disease. Patients, who presented to the emergency room at least 4 but no more than 24 hours after the onset of a painful vasoocclusive crisis severe enough to require hospitalization, were considered candidates for the study. Each patient received either placebo or cetiedil at one of the following three dosages: 0.2, 0.3, or 0.4 mg/kg body weight. The assigned drug dosage was given as a 30 minute intravenous infusion every 8 hours for 4 consecutive days. A total of 67 patients was enrolled in the study. Cetiedil, at its highest dosage (0.4 mg/kg body weight), was found to be significantly superior to placebo both in reducing the number of painful sites present on all 4 treatment days and in shortening the total time in crisis. No serious adverse reactions were observed during the course of the study. We conclude that cetiedil, given at a dosage of 0.4 mg/kg body weight, is therapeutically advantageous for sickle cell crisis.[1]

References

  1. A collaborative, double-blind randomized study of cetiedil citrate in sickle cell crisis. Benjamin, L.J., Berkowitz, L.R., Orringer, E., Mankad, V.N., Prasad, A.S., Lewkow, L.M., Chillar, R.K., Peterson, C.M. Blood (1986) [Pubmed]
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