Overview
Treatment of Functional Dyspepsia With Genuine Regional Rhizoma Atractylodis
Status:
Unknown status
Unknown status
Trial end date:
2018-08-01
2018-08-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is a randomized double-blind placebo controlled trial aim to compare the efficiency of genuine regional and non-genuine regional Rhizoma Atractylodis in treating functional dyspepsia. This study will also observe the clinical safety of genuine regional Rhizoma Atractylodis.The trial will be conducted in Xiyuan Hospital of China Academy of Chinese Medicine Sciences and Dongzhimen Hospital of Beijing University of Chinese Medicine.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
China Academy of Chinese Medical Sciences
Criteria
Inclusion Criteria:1. Meeting the FD Rome Ⅲ diagnosis standard;
2. Meeting TCM differentiated diagnosis standard of the spleen deficiency with dampness
pattern;
3. Without taking any medicines affecting gastric motility in the recent 14 days;
4. Between 18 and 65 years old;
5. Voluntary participation in the trial and signing informed consent.
Exclusion Criteria:
1. Combined irritable bowel syndromes; combined peptic ulcer, erosive gastritis, atrophic
gastritis, abdominal surgery history, gastric mucosa with severe dysplasia or
pathological diagnosis of suspected malignant transformation; combined
gastroesophageal reflux disease, irritable bowel syndrome with overlapping syndromes.
2. Patient whose differentiation is not clear or who doesn't belong to the spleen
deficiency with dampness pattern.
3. Women in pregnancy, breastfeeding or have fertility plans recently; the legally
disabled (blind, deaf, dumb, mental retardation, mental disorders, physical
disability)
4. Patients with endocrine and metabolic diseases such as connective tissue diseases,
diabetes, menopausal syndromes; patients combined with heart rate disorder, severe
diseases in cardiovascular, brain, liver, lung, kidney and hematopoietic systems,
acute and chronic infectious diseases, malignant tumors, mental illness.
5. Allergy to the trial drug.
6. With suspected or definite alcohol, drug abuse history.