functional dyspepsia
Conditions
Interventions
treatment group:Shu Mu's acupoint combination massage technique
Sponsors
Affiliated Hospital of Liaoning University of Chinese Medicine
Eligibility
Sex/Gender
All
Age
No minimum to 3 Years
Inclusion criteria
Inclusion criteria: Only those who meet all the following conditions can be selected for the study: 1. Meet the diagnostic criteria for functional dyspepsia in infants according to both traditional Chinese medicine and Western medicine; 2. The traditional Chinese medicine diagnosis is milk and food stagnation syndrome/spleen deficiency and food stagnation syndrome; 3. Aged 0 to 3 years old (=3 years old), with no gender restrictions; 4. Agree to cooperate with treatment and accept evaluation according to the requirements of the trial protocol; 5. The informed consent of the legal guardian of the subject must be obtained and the informed consent form must be voluntarily signed; when the subject is capable of making decisions regarding participation in clinical trials, the consent of the subject himself/herself must also be obtained. Those who do not meet any of the above conditions shall not be selected as subjects.
Exclusion criteria
Exclusion criteria: Studies that meet any of the following criteria should be excluded: 1. Indigestion caused by organic diseases, such as acute or chronic gastroenteritis, peptic ulcer, history of gastrointestinal surgery, acute or chronic hepatitis, anorexia nervosa, and anorexia caused by certain medications; 2. Accompanied by fever, with a body temperature >38?, or accompanied by moderate or severe dehydration; 2. Moderate to severe malnutrition; 3. There are contraindications to massage such as local skin infections, lesions, burns, or skin diseases (such as eczema, herpes) that affect the area where massage is performed; 4. Presence of severe primary diseases in cardiovascular, neurological, respiratory, hepatobiliary, urinary systems, etc; 5. Mental disorders, intellectual disabilities, and/or communication disorders; 6. Participants who have participated in other clinical trials within the previous 3 months prior to the trial; 7. Individuals whom the researchers deem unsuitable for participation in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall effective rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Disappearance rate of clinical single symptom;Effective rate of clinical single symptom;Total Symptom Score;Scores for individual symptoms;Traditional Chinese Medicine (TCM) syndrome score;Growth and nutritional status indicators (height, weight, body mass index); | — |
Countries
china
Contacts
Public Contactwangxuefeng
Affiliated Hospital of Liaoning University of Chinese Medicine
Outcome results
None listed