CTRI/2022/01/039227已完成未知
Efficacy of Nicorandil as an add-on therapy to standard treatment in acute ischemic stroke- A Randomized, single blind, controlled clinical trial - ENCORE
SRMIST0 个研究点目标入组 19 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 19
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
- •Age 18 -75 years.
- •-Both genders.
- •-Diagnosis of acute ischemic stroke.
- •-More than 24 hours of onset of symptoms and not greater than 96 hours.
- •-Modified Rankin scale greater than two.
- •-Ability to ingest oral medication.
- •-BMI >18.5 kg /m².
排除标准
- •Haemorrhagic stroke.
- •Hypotension with a SBP < 100 mmHg.
- •Patients on ACEIs and ARBs.
- •Patients on steroids.
- •Patients with respiratory compromise.
- •Patients on antidepressant drugs.
- •Severe acid peptic disease.
- •Kidney dysfunction (GFR < 30ml /min).
- •Intake of NSAID (exemption of Paracetamol).
- •Severe unstable medical illnesses, including uncontrolled cardiac conditions or heart failure, cardiogenic shock (New York Heart Association Class III or IV).
- •Use of any investigational agents within 30 days prior to screening.
- •Pregnant women and lactating mothers.
- •Severe hypovolemia.
- •Severe liver dysfunction.
- •Severe bradycardia ( <50 bpm).
- •Patients with G6PD deficiency.
- •Clotting factor Deficiency
研究者
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