AIDS patients /HIV carriers
Conditions
Interventions
Control Group:Daily diet or homemade liquid food support program
Experimental Group:Enteral nutrition (Shanghai Licheng nutrition products technology co., LTD.)
Sponsors
The First Affiliated Hospital of Kunming Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with AIDS; 2. Male or female, aged >= 18 years; 3. Patients who can persist in nutrition support treatment for more than 3 months; 4. AIDS patients with nutritional treatment indications; 5. Informed consent of patients / relatives to participate in the study.
Exclusion criteria
Exclusion criteria: 1. The patient was contraindicated to enteral and parenteral nutrition and was known to be allergic to any component of parenteral nutrition for research; 2. Patients with Apache II score > 10; 3. Patients with severe liver, kidney, heart, brain dysfunction, or severe complications such as hypertension, diabetes, coronary heart disease, etc. Patients with severe acute infection, uncontrolled infection, or thickening and chronic infection, and delayed wound healing. Patients with central nervous metastases whose condition was not controlled and had obvious intracranial hypertension or neuropsychiatric symptoms; 4. Patients who participated in other clinical studies; 5. Patients who are known to be in pregnancy or lactation; 6. Patients with poor compliance and unable to cooperate with treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| lymphocyte subpopulation;viral load;LPS/D - lactic acid/DAO;cytokines;feces 16S DNA sequencing; | — |
Secondary
| Measure | Time frame |
|---|---|
| blood routine examination;blood biochemistry; | — |
Countries
China
Contacts
Public ContactKunhua Wang
The First Affiliated Hospital of Kunming Medical University
Outcome results
None listed