IRCT20130812014333N145招募中3 期
Comparative assessment of the efficacy and safety of add ontreatment with Sofosbuvir plus Velpatasvir” to standard of care therapeutic regimen” in patients with COVID-19
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 80
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
- 18 years 至 no limit（—）
- 性别
- All
入选标准
- •Age over 18 years
- •Absolute lymphocyte count <1100 / ML or SaO2 <93
排除标准
- •Pregnancy or breast-feeding
- •The physician's decision that the trial is not in the patient's interest
- •Any circumstances that do not allow to follow the treatment protocol easily
- •A history of severe liver disease including cirrhosis or ALT or AST levels more than fives times normal
- •Drugs that are contraindicated with standard treatment or Sofosbuvir-Velpatasvir and cannot be discontinued
- •History of untreated HIV infection or hepatitis C
研究者
相似试验
招募中
3 期
Comparative assessment of the efficacy and safety of addon treatment with Sofosbuvir-Daclatasvir”, Lithium”,and Trifluoprazine” to standard of care in three groups of patients with COVID-19IRCT20130812014333N147Kermanshah University of Medical Sciences80
进行中（未招募）
不适用
Dexmedetomedine intravenous sedation on patients with and without Beta blockersCTRI/2018/08/015387ETHRADHAMA SUPER SPECIALITY EYE HOSPITA
招募中
2 期
evaluation the effect of botulinum toxin type A for treating frown linesskin rejuvenation.IRCT20150101020514N8Imen vaccine alborz Company140
已完成
不适用
Comparative evaluation of the safety and efficacy of long term use of anti-cholinergic, Imidafenacin and Solifenacin, on overactive bladder: a prospective randomized trial.overactive bladderJPRN-UMIN000004354Department of Urology, Kanto Rosai Hospital60
尚未招募
4 期
Comparison of adhesive and suture in skin closure following small incision abdominal surgery(laparoscopic)CTRI/2024/07/070591Adichunchanagiri Institute Of Medical Sciences