MedPath

Clinical study on the effect of Yi-Gong-San on the prognosis of patients with chronic anemia and sepsis

Phase 1
Recruiting
Conditions
Sepsis accompanied by chronic anemia
Registration Number
ITMCTR2100004518
Lead Sponsor
Baoshan Branch of Shuguang Hospital Affiliated to Shanghai University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(1) Definitely diagnosed as sepsis related ACD;
(2) Moderate or mild anemia (male :60g/L < Hb < 120g/L, female :60g/L < Hb < 110g/L);
(3) Older than 18 years old;
(4) Volunteered to participate in the clinical trial and signed the informed consent.

Exclusion Criteria

(1) Being treated with iron and/or EPO;
(2) Known iron metabolic diseases;
(3) Malignant tumor or immune system disease is found after hospitalization;
(4) Transfusion during hospitalization (to avoid the effects of unnecessary transfusion on hemoglobin and anemia-related parameters);
(5) Other diseases causing anemia (aplastic anemia, iron deficiency anemia, hemolytic anemia, etc.) have been diagnosed before admission;
(6) Significant blood loss (such as gastrointestinal bleeding);
(7) Trauma
(8) Chronic liver failure or chronic renal insufficiency caused by other causes;
(9) Abandonment of treatment.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
In-hospital mortality rate;
Secondary Outcome Measures
NameTimeMethod
HO-1;IFN-?;Hb;SOFA score;IL-17a;sTfR;SI;TNF-a;IL-2;TSAT;Hepcidin;RDW;APACHEII score;IL-4;IL-6;SF;IL-10;TIBC;
© Copyright 2025. All Rights Reserved by MedPath