A randomized placebo control study to evaluate the effect of AYUSH SR as adjunct to usual care for cardiac rehabilitation on biochemical, physical and psychological parameters, in adult patients who underwent Coronary Artery Bypass Graft (CABG) - Nil

Central Council for Research in Ayurvedic Science (CCRAS) Ministry of AYUSH, Government of India0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年9月18日

试验速览

暂无简介。

•1.Patients admitted for CABG surgery
•2.Male or female patient’s between 18-65 years of age.
•3.Subjects who underwent CABG surgery within the last 5 days with a relatively uncomplicated perioperative period
•4.Subjects ready to give informed written consent
•5.Subjects willing for follow up till 3 months after the intervention.

•1.Subjects with severe respiratory or cardiac compromise, uncontrolled Pulmonary Dysfunction (asthmatic and COPD patients) or other concurrent severe disease or active infection.
•2. complications during CABG surgery such as prolonged requirement for mechanical ventilation, acute kidney injury, and bleeding requiring transfusion or reoperation etc that may affect the clinical outcome in patients may also be excluded in the trial
•3.History or diagnosis of sleep disorder, use of any other medicines with similar effect to that of AYUSH SR or using any other herbal medicines will be excluded.
•4.Subjects with history of or current neurological or psychiatric impairment, or cognitive dysfunction that could compromise data collection.
•5. Patients with any concurrent hepatic disorder (defined as liver enzymes SGOT/SGPT >2 times upper normal limit) or Renal Disorders (defined as S.Creatinine >1.4mg/dl).
•6.Patients with poorly controlled Hypertension ( >160/100 mm of Hg) & poorly controlled Diabetes Mellitus (HbA1c >8.0%) may be excluded

发起方

Central Council for Research in Ayurvedic Science (CCRAS) Ministry of AYUSH, Government of India