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临床试验/RPCEC00000214
RPCEC00000214尚未招募1 期

Co-administration of EGF and GHRP-6 in patients with acute cerebral infarction of ischemic etiology.

Center for Genetic Engineering and Biotechnology (CIGB), in Havana0 个研究点目标入组 30 人开始时间: 2016年5月27日最近更新:
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
分配方式
Randomized controlled trial. Masking: Open. Control group: Active. Assignment: Parallel. Purpose: Treatment

入排标准

年龄范围
18 years 至 80 years(—)
性别
All

入选标准

  • 1. Compliance with the diagnostic criteria (patients of both sexes with a focal neurologic defects caused by disturbances in blood supply to a particular brain area).
  • 2. Age between 18 and 80 years, including both.
  • 3. Time between onset of symptoms and start of administration of CIGB-845 less than 12 hours.
  • 4. Willingness of the patient (or family) through the granting of informed consent (oral). In a second moment (once the patient is stabilized) the investigator must obtain the written consent of the patient, who may freely decide whether to accept or not to continue the investigation.

排除标准

  • 1. Coma (Glasgow Coma Scale less than 8).
  • 2. Points in the NIHSS <5 or> 20 scale.
  • 3. When the neurological defect can be explained by a different entity to ICA.
  • 4. Patients with neurological symptoms or signs return to normal before treatment begins.
  • 5. Severe uncontrolled hypertension (systolic> 185 mm Hg or diastolic BP> 110 mm Hg) not descend after treatment.
  • 6. Low blood pressure (systolic <95 mm Hg) unresponsive to standard therapy.
  • 7. Method of installation box with seizures.
  • 8. Patients diagnosed with malignancies.
  • 9. Pregnancy or breastfeeding at the time of inclusion in the study (reported by the patient or family).
  • 10. Mental incapacity obvious to issue consent and act accordingly to the study.

研究者

发起方
Center for Genetic Engineering and Biotechnology (CIGB), in Havana

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