About this trial
To evaluate the improvement of symptoms in patients with gastroesophageal reflux disease combined with depression (hepatic and gastric depression-heat type) by Zuojin Wan combined with vornodine fumarate regimen as a control, and to compare the adherence to the medication and the adverse reactions of the patients between the two groups.
Eligibility criteria
Qualifiers
Aged between 18 and 65 years;
Fulfilment of western medical diagnostic criteria for GERD;
Meet the diagnostic criteria for mild depression;
Comply with the diagnostic criteria of Liver and Stomach Depression-Heat syndrome in Chinese medicine;
Disqualifiers
HP positive patients;
Other organic diseases of the digestive system, such as peptic ulcer, peptic tumour, peptic haemorrhage, liver, gallbladder and pancreas disease, intestinal obstruction and inflammatory bowel disease;
Systemic diseases affecting the dynamics of the digestive tract, such as diabetes mellitus, chronic renal insufficiency, connective tissue diseases, neurological lesions, etc;
Pathological diagnosis of the esophageal mucosa suggestive of moderate-to-severe heterogeneous hyperplasia;
Trial design
Treatments tested in this trial
- Vonorasan Fumarate
- Zuojin Pills