Skip to content

Study on the development mechanism of deficiency sepsis in the elderly based on the obstacle of inflammatory regression and the intervention effect of the method of supporting and replenishing the deficiency

Study on the development mechanism of deficiency sepsis in the elderly based on the obstacle of inflammatory regression and the intervention effect of the method of supporting and replenishing the deficiency

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025002109
Enrollment
Unknown
Registered
2025-11-04
Start date
2024-11-05
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sepsis

Interventions

Elderly Healthy Control Group:none
Non-elderly Sepsis Group:none
Elderly Sepsis Group:none

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1)age=18 years 2)Patients diagnosed with sepsis according to the Guidelines for the emergency treatment of sepsis/septic shock in China (2018) were included in this study which with infection and Sequential Organ Failure Assessment (SOFA) score = 2

Exclusion criteria

Exclusion criteria: 1)patients with malignant tumors; 2)Patients with known immunodeficiency such as organ or bone marrow transplantation HIV infection or those who have taken immunosuppressants in the last 3 months; 3)Serious primary diseases of the hematologic system such as leukemiamyelodysplastic syndromes and idiopathic thrombocytopenic purpera etc. 4)Have severe liver or kidney dysfunction(defined as a SOFA score of =3 for liver or kidney) 5)Subjects who in the judgement of the investigator are not suitable for participation in the study. For example poor adherence lack of willingness to treat etc. 6)Have participated in other clinical investigators within the last 30 days; 7)Pregnant or lactating women; 8)Patients who did not sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Specialized pro-resolving mediators(SPMs);Collection of TCM syndromes in clinical practice;

Secondary

MeasureTime frame
Blood routine indicators;Coagulation indicators;Demographic information;Comorbidity;History of present illness;Plasma cytokines;Immunity-related indicators;Blood gas analysis;Abdominal CT; Vital signs;Inflammation-related indicators;Collection of follow-up data for endpoint indicators;Biochemistry;

Countries

China

Contacts

Public ContactHuayang Cai

Guangdong Provincial Hospital of Chinese Medicine

caihuayang@gzucm.edu.cn+86 20 8188 7233

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026