Tuberculosis
Conditions
Interventions
Experiment group 1:Oral nutrition powder 1
Experiment group 2:Oral nutrition powder 2
control group:Oral TP
Sponsors
Beijing Chest Hospital, Capital Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1.a. Age = 18 years old =80 years old; 2.b. Patients with tuberculosis; 3.c. The risk screening scores of management and nutrition were 3-5 points, with nutritional risk and ALB < 35g/L; 4.d. Understand the informed consent and agree to sign the informed consent prior to this study;
Exclusion criteria
Exclusion criteria: a. Any serious medical condition other than pulmonary tuberculosis, such as heart failure, severe liver and kidney dysfunction, that was considered by the investigator to be likely to affect treatment, follow-up, or evaluation. b. The patient had a history of alcohol and drug abuse, which was considered by the investigator to be unable to adhere to the protocol or affect the results of the analysis. c. Patients with nasal feeding, parenteral nutrition support, or oral nutrition supplement with energy requirements higher than 600kcal.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| albumin; | — |
Secondary
| Measure | Time frame |
|---|---|
| Nutritional risk score;Hospitalization days, hospitalization expenses, and adverse events during hospitalization;Hemoglobin (HB), lymphocyte percentage (L%), C-reactive protein (CRP), respiratory quotient, oxygen partial pressure, T cell count, etc; | — |
Countries
China
Contacts
Public ContactMa Jiaojie
Beijing Chest Hospital, Capital Medical University
Outcome results
None listed