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Effect of PGJX Decoction on Fluid Resuscitation and Vascular Endothelial Function in Patients With Septic Shock

Effect of PGJX Decoction on Fluid Resuscitation and Vascular Endothelial Function in Patients With Septic Shock

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001495
Enrollment
Unknown
Registered
2025-07-26
Start date
2024-02-05
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Septic Shock

Interventions

Treatment group:Oral administration of Pogejixin Decoction was administered in addition to conventional Western medical treatment.
Control group:Empirical antibiotic therapy as well as fluid resuscitation and vasopressor administration for symptomatic management.

Sponsors

Foshan Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1)Patients who meet the diagnostic criteria for septic shock;(2)Aged 18 to 80 years;(3)Patients who are diagnosed with Yang Qi deficiency and collapse or Yin depletion with Yang collapse according to Traditional Chinese Medicine (TCM) differentiation;(4)The research content must be reviewed and approved by the Medical Ethics Committee of our hospital. Only those patients who have provided informed consent either by themselves or through their family members and have signed the consent form are eligible.

Exclusion criteria

Exclusion criteria: (1)Individuals who do not meet the inclusion criteria fail to follow the prescribed medication regimen or have incomplete data that affects the assessment of therapeutic efficacy; (2)Patients with gastrointestinal perforation or severe gastrointestinal dysfunction with a gastrointestinal function score of 3 who are unable to receive enteral medications; (3)Patients with acute or chronic renal failure requiring continuous blood purification;(4)Patients with severe underlying diseases such as cardiomyopathy acute myocardial infarction massive pulmonary embolism acute cerebrovascular accident or Stage IV malignant tumors;(5)Pregnant women or those who have been taking immunosuppressive agents long-term or those who require high-dose corticosteroids due to their medical condition;(6)Patients or their family members who do not agree.

Design outcomes

Primary

MeasureTime frame
Length of Stay;Vascular Endothelial Growth Factor(VEGF);Nitric Oxide(NO);Lactate(Lac);Soluble Thrombomodulin(sTM);Heart Rate(HR);6-Keto-Prostaglandin F1a(6-keto-PGF1a);Daily Fluid Requirement;Blood Pressure(BP);Daily Vasopressor Dosing;SOFA Score;APACHEII Score;Endothelium-Derived Relaxing Factor(EDRF);28-Day Mortality Rate;Duration of Vasopressor Therapy;

Secondary

MeasureTime frame
Procalcitonin(PCT);White Blood Cell Count(WBC);Neutrophil Percentage(NEUT%);

Countries

China

Contacts

Public ContactQiusheng Xiao

Foshan Hospital of Traditional Chinese Medicine

43094665@qq.com13925460524

Outcome results

None listed

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