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NCT07781436
A Randomized Controlled Trial: Fuzheng Yangxin Formula for ERAS After CABG
Conditions: CAD - Coronary Artery Disease, CABG, ERAS, Medicine, Chinese Traditional
Sex: All
Ages: 20 Years – 80 Years
Healthy volunteers: No
Phase: NA
Enrollment: 230
Sponsor: Peking University Third Hospital
Location: Peking University 3rd hospital Beijing
Summary
This study aims to evaluate the efficacy and safety of Fuzheng Yangxin Formula (FZYXF) in the treatment of qi-yin deficiency syndrome after coronary artery bypass grafting (CABG), formulate an integrated Chinese and Western medicine rehabilitation protocol, develop special proprietary Chinese medicines for postoperative patients, establish a postoperative rehabilitation database, and promote the standardized application and achievement transformation of integrated Chinese and Western medicine therapy in cardiac surgery.
Eligibility Criteria
Inclusion Criteria:
-Patients who have undergone coronary artery bypass grafting (CABG) and present with postoperative qi-yin deficiency syndrome.
Exclusion Criteria:
* Patients with hypersensitivity to any components of Fuzheng Yangxin Formula granules.
* Patients with fever or common cold after surgery.
* Patients with severe postoperative liver and kidney dysfunction.
* Patients who receive concurrent valve surgery or other intracardiac operations
* Patients with end-stage malignant tumors
* Patients with uncontrolled infection or bleeding
* Patients with progressive degenerative systemic diseases, such as severe trauma, multiple organ failure and other severe impairment of vital organ function including severely damaged liver function
* Patients with severe heart failure or cardiogenic shock who cannot tolerate treatment.
Source: ClinicalTrials.gov (NCT07781436). StuddyBuddy aggregates publicly available trial information.