Severe pneumonia
Conditions
Interventions
Control group:Qi-Gui-Yin placebo granules, 200 ml/time and 2 times/day
Experimental group:Qi-Gui-Yin formula granules, 200 ml/time, 2 times/day
Sponsors
Beijing institute of Traditional Chinese Medicine
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: (1) meet the diagnostic criteria of severe pneumonia; (2) Aged 18 to 80 years; (3) patients or their families are aware of the study content and sign the informed consent voluntarily.
Exclusion criteria
Exclusion criteria: (1) pregnancy or pregnancy preparation, or unable to take effective measures to prevent pregnancy; (2) persons with serious mental disorders; (3) the expected survival time of patients due to basic diseases is less than 28 days, such as poor control of malignant tumors and cardiac arrest within 30 days in the past; (4) plant survival state; (5) confirmed or highly suspected acute infectious diseases, such as viral hepatitis active stage, active stage tuberculosis, etc.; (6) allergy to the effective ingredients or auxiliary materials of the test drugs; (7) participated in clinical intervention trials in the past 3 months; (8) subjects who are considered unfit to participate in this study by the attending doctor.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 28-day mortality; | — |
Secondary
| Measure | Time frame |
|---|---|
| Mechanical ventilation time;Length of ICU stays;Antibiotic DDD value;Length of hospital stays;PSI Score;SOFA Score;CRP;PCT;Sputum specimen culture; | — |
Countries
China
Contacts
Public ContactLiu Qingquan
Beijing Hospital of Traditional Chinese Medicine affiliated to Capital Medical University/Beijing institute of Traditional Chinese Medicine
Outcome results
None listed