IRCT20180619040147N6尚未招募1 期
Safety and efficacy study of allogeneic human menstrual blood stem cells secretome to treat severe Covid-19 patients, clinical trial phase I&II
Iranian academic center for education culture and research0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
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
- 年龄范围
- 40 years 至 65 years(—)
- 性别
- All
入选标准
- •Aged 40-65 years
- •Voluntarily participate in this clinical trial and sign off informed consent form
- •Chest imaging confirm COVID-19 featured lesions in the lung
- •The SARS-CoV-2 nucleic acid test was positive
- •Diagnosed with severe pneumonia of COVID-19: respiratory distress, Respiratory rate (RR) = 30 times/min; resting oxygen saturation of 90% or less; arterial pressure of oxygen/the fraction of inspired oxygen= 300 mmHg; pulmonary imaging of focus within 24-48 hours > 50% progression
排除标准
- •History of drug reactions or allergies
- •Pneumonia caused by bacteria, Mycoplasma, Chlamydia, Legionella, fungi, or other viruses
- •Airway obstruction due to lung cancer or unknown factors
- •Carcinoid syndrome
- •History of epilepsy and long-term use of anticonvulsant drugs during the last 3 years
- •History of long-term use of immunosuppressive drugs
- •History of chronic respiratory illness that requires long-term oxygen therapy
- •The patient is on blood or peritoneal dialysis
- •Creatinine clearance <15 ml / min
- •Moderate to severe liver disease (Child-Pugh score> 12)
- •History of deep vein thrombosis (DVT) or pulmonary embolism over the past 3 years
- •Being under ECMO or high-frequency oscillatory ventilation support
- •Diagnostic of HIV, hepatitis B, and syphilis
- •Pregnant or lactating women
- •Lack of consciousness and inability to provide informed consent by the patient
研究者
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