跳至主要内容
临床试验/CTRI/2020/11/028779
CTRI/2020/11/028779进行中(未招募)1 期

A phase I, open label, parallel, randomised trial to assess the safety and efficacy of SARS-CoV-2 Equine Antiserum Immunoglobulin (Purified F(ab)2 fragment) in hospitalised COVID-19 patients with moderate disease in addition to standard of care. - None

Biological ELimited0 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
1 期
状态
进行中(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. Both male and female patients aged between 18-55 years who signed the informed consent.
  • 2. Patients screened for Covid-19 by RT-PCR method <=72 hours from the date
  • of RT-PCR confirmation and/or 7 days from the start of symptoms.
  • 3. Respiratory Rate > 24 breaths/min and SpO2 <=93% on room air
  • 4. Patients screened for intradermal sensitivity testing prior to initiation of infusion.

排除标准

  • 1.Pregnant women
  • 2. Breastfeeding women
  • 3. Known hypersensitivity to blood products and reactive to intradermal
  • sensitivity test prior to infusion
  • 4. Receipt of pooled immunoglobulin in last 30 days
  • 5. Critically ill patients:
  • a. Severe ARDS cases
  • b. Shock (Requiring Vasopressor to maintain a
  • MAP >= 65mmHg or MAP below 65)
  • 6. Participating in any other clinical trial
  • 7. Clinical status precluding infusion of blood
  • 8. Patients are not suitable for transfusion
  • 9. Patients with severe pneumonia defined as: RR
  • >=30 times/min or oxygen saturation <= 90% in
  • resting state or PaO2/FiO2 <= 100 mmHg or
  • respiratory failure and mechanical ventilation
  • are required or shock occurs or ICU
  • monitoring with presence of other organ
  • 10. Acute life-threatening organ dysfunction
  • caused by a dys-regulated host response to
  • suspected or proven infection. (Signs of organ
  • dysfunction include: altered mental status,
  • difficult or fast breathing, low oxygen
  • saturation, reduced urine output, fast heart
  • rate, weak pulse, cold extremities
  • or low blood pressure, skin mottling, or
  • laboratory evidence of coagulopathy,
  • thrombocytopenia, acidosis, high lactate or
  • hyperbilirubinemia).
  • 11. Patients on any other immunoglobulin or
  • immunomodulatory treatment;
  • 12. Patients with known history of allergy to
  • horse proteins or severe allergic reactions
  • to any component of the Equine antiserum;

研究者

发起方
Biological ELimited

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