Assessment on Effects of Tongjiang Granule in Treating Nonerosive Reflux Disease Overlapping Epigastric Pain Syndrome
NCT ID: NCT05312463
Last Updated: 2022-04-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE1/PHASE2
228 participants
INTERVENTIONAL
2022-03-26
2024-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Tongjiang granule group
Experiment group: oral administration of Tongjiang granule with warm water after meal for 1 bag each time for three times a day. The medication period was 4 weeks.
Tongjiang granule
Tongjiang granules, 1 bag / time, 3 times / day.
Tongjiang granule simulant group
Control group:oral administration of Tongjiang granule simulant with warm water after meal for 1 bag each time for three times a day. The medication period was 4 weeks.
Tongjiang granule simulant
Tongjiang granule simulant,1 bag / time, 3 times / day.
Interventions
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Tongjiang granule
Tongjiang granules, 1 bag / time, 3 times / day.
Tongjiang granule simulant
Tongjiang granule simulant,1 bag / time, 3 times / day.
Eligibility Criteria
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Inclusion Criteria
2. It meets the diagnostic criteria of liver-stomach depression-heat syndrome of traditional Chinese medicine
3. Age between 18 and 70 years old
4. Patients have informed consent and are willing to receive corresponding treatment
Exclusion Criteria
2. There are other organic diseases of the digestive system (such as acute and chronic pancreatitis, cirrhosis, etc.), or systemic diseases that affect the gastrointestinal motility, such as hyperthyroidism, diabetes mellitus over 10 years, chronic renal insufficiency, spirit (the score of SAS and SDS shows severe anxiety or depression), nervous system diseases, etc
3. Patients with severe organ diseases such as heart, liver and kidney (such as ALT, AST more than 2 times of normal value), hematopoietic system diseases and tumors
4. HP infection was positive (bacterial culture, histological examination, urea breath test, rapid urease test and fecal antigen test were positive);
5. People with a history of gastric / abdominal surgery (excluding appendectomy);
6. Pregnant and lactating women;
7. People with a history of allergies to all the test drugs
8. Subjects who are participating in other clinical trials or have participated in other clinical trials within 4 weeks
9. Other situations that reduce the possibility of enrollment or complicate enrollment according to the judgment of the researcher, such as frequent changes in working environment and other situations that are easy to cause loss of follow-up.
18 Years
70 Years
ALL
No
Sponsors
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First Affiliated Hospital of Heilongjiang Chinese Medicine University
OTHER
Yueyang Hospital of Integrated Traditional Chinese and Western Medicine
UNKNOWN
Liuzhou Hospital of Traditional Chinese Medicine
OTHER
Xiyuan Hospital of China Academy of Chinese Medical Sciences
OTHER
Responsible Party
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Locations
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Xiyuan Hospital of China Academy of Chinese Medical Sciences
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2021XLA117-3
Identifier Type: -
Identifier Source: org_study_id
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