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DOI 10.1016/j.amjmed.2014.03.019

Медицинская библиотека · The American journal of medicine · 2014

Randomized controlled trial of sildenafil for preventing recurrent ischemic priapism in sickle cell disease.

Burnett Arthur L, Anele Uzoma A, Trueheart Irene N, Strouse John J, Casella James F

Клиническое исследование II фазыСтатьяРандомизированное исследованиеПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

BACKGROUND

Successful preventive therapy for ischemic priapism, a disorder of penile erection with major physical and psychologic consequences, is limited. We conducted a randomized, double-blind, placebo-controlled clinical trial to assess the efficacy and safety of sildenafil by a systematic dosing protocol to prevent recurrent ischemic priapism associated with sickle cell disease.

METHODS

Thirteen patients with sickle cell disease reporting priapism recurrences at least twice weekly were randomized to receive sildenafil 50 mg or placebo daily, unassociated with sleep or sexual activity, for 8 weeks, followed by open-label use of this sildenafil regimen for an additional 8 weeks.

RESULTS

Priapism frequency reduction by 50% did not differ between sildenafil and placebo groups by intention-to-treat or per protocol analyses (P = 1.0). However, during open-label assessment, 5 of 8 patients (62.5%) by intention-to-treat analysis and 2 of 3 patients (66.7%) by per protocol analysis met this primary efficacy outcome. No significant differences were found between study groups in rates of adverse effects, although major priapism episodes were decreased 4-fold in patients monitored "on-treatment."

CONCLUSIONS

Sildenafil use by systematic dosing may offer a strategy to prevent recurrent ischemic priapism in patients with sickle cell disease.

Для цитирования: Burnett Arthur L, Anele Uzoma A, Trueheart Irene N, Strouse John J, Casella James F. Randomized controlled trial of sildenafil for preventing recurrent ischemic priapism in sickle cell disease.. The American journal of medicine. 2014. DOI: 10.1016/j.amjmed.2014.03.019.

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