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临床试验/CTRI/2024/08/072499
CTRI/2024/08/072499尚未招募2 期

Evaluation of efficacy and safety of adjuvant Pentoxifylline therapy in adults with community acquired pneumonia: An Open label, Randomized-controlled trial. - NI

SARANDEV A T V0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1)At least one acute clinical sign compatible with pneumonia (dyspnea, cough, purulent sputum, crackles)
  • 2)Infiltrate on chest X-ray or CT scan suggestive of pneumonia
  • 3)Diagnosis of CAP at or during the 48 hours post-hospital admission.
  • 4)Informed consent signed by the patient, his/her legally authorized representative.

排除标准

  • 1)Patient on invasive mechanical ventilation.
  • 2)Patients with creatinine clearance less than 30 ml per minute
  • 3)Patient on vasopressors at the time of inclusion
  • 4)Any contraindications to the study drug
  • 5)Patient requiring corticosteroids (except for nebulized corticosteroids) for any reason.
  • 6)Patient treated with antibiotics for more than 7 days prior to admission.
  • 7)Suspicion of aspiration or heath care associated pneumonia.
  • 8)Active tuberculosis
  • 9)On immunosuppressive therapy or malignancy
  • 10)Pregnancy or lactating women

研究者

发起方
SARANDEV A T V

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