Functional Dyspepsia Syndrome in Children
Conditions
Interventions
intervention group:medicinal and food homology baked biscuits
control group:placebo baked biscuits
Sponsors
Chengdu Women and Children's Central Hospital
Eligibility
Sex/Gender
All
Age
1 Years to 3 Years
Inclusion criteria
Inclusion criteria: 1: Meeting the diagnostic criteria for decreased appetite in children with functional dyspepsia syndrome in Western medicine, with or without the other four clinical manifestations 2: (1) Clinical manifestations and diagnosis of pediatric stasis in traditional Chinese medicine 3: (2) Age range from 1 to 3 years old 4: (3) Within one month before enrollment, who had not used any other traditional Chinese medicine for dispelling accumulation, dissipating stagnation and clearing heat, as well as Prokinetic agent, antacid or antacid drugs 5: (4) The family members or primary guardians of the child agree to participate in the study and sign a written consent form 6: (5) Regularly participate in physical examination and regular follow-up at local medical institutions, and receive feeding suggestions and nutrition guidance from child care physicians, dietitian, and traditional Chinese medicine practitioners.
Exclusion criteria
Exclusion criteria: 1: (1) At the time of enrollment, there were warning symptoms of gastrointestinal diseases, such as frequent vomiting, hematemesis, apnea, growth retardation, difficulty feeding or swallowing, painful expression or abnormal posture, fever, bloody stools, changes in complexion, dehydration, difficulty in meconium excretion, etc 2: (2) Those who have severe systemic diseases such as heart, brain, liver, kidney, endocrine, and blood at the time of enrollment 3: (3) Allergic constitution and allergy to test drug 4: (4) The children with symptoms caused by intestinal stricture and rectal and colonic organic diseases (such as tumor, inflammation, anal fissure, Crohn's disease, Bowel obstruction, intestinal adhesion, colonic polyps, intestinal tuberculosis, etc.) were determined at the time of enrollment 5: (5) Disabled children (blind, deaf, mute, intellectual disabilities, mental disorders) as stipulated by law 6: (6) Participated in other clinical researchers within the past three months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| children's growth and development;Family Quality of Life Survey; | — |
Secondary
| Measure | Time frame |
|---|---|
| dietary survey; | — |
Countries
China
Contacts
Public ContactChen Ke
Chengdu Women and Children's Central Hospital
Outcome results
None listed