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Effects of Fusu mixture (Wen-Shen-Qian-Yang Method) on sepsis-induced acute respiratory distress syndrome

Effects of Fusu mixture (Wen-Shen-Qian-Yang Method) on sepsis-induced acute respiratory distress syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002812
Enrollment
Unknown
Registered
2019-12-07
Start date
2020-01-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Acute lung injury with sepsis

Interventions

Sponsors

Affiliated Hospital of Chengdu University of traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) The patient's aged 18-80 years; (2) The course of disease is within 12-48 hours, which meets the diagnostic criteria for sepsis and acute lung injury [28,29,30]; (3) Oxygenation index (PaO2 / FiO2) <=200 at ARDS; (4) Patients with mechanical ventilation; (5) The study complies with the Helsin Declaration and Chinese clinical trial research regulations. The patient or his family knows the research content and voluntarily signs the informed consent form.

Exclusion criteria

Exclusion criteria: (1) pregnant and lactating women; (2) Those who are allergic to the drugs used in the program; (3) Those with surgical indications; (4) Patients with other serious physical diseases, AIDS, and malignant tumors; (5) Patients who are expected to die or give up active rescue within 12 hours of entering the ICU and are unwilling to undergo conventional supportive treatment by Western medicine; (6) Patients with contraindications to femoral artery catheterization, patients with contraindication to central venous catheter placement, and patients with contraindications to blood transfusion (7) Patients with chronic heart failure or end-stage multiple organ failure; (8) currently participating in other drug researchers; (9) An employee of the research site or a family member of an employee of the research site.

Design outcomes

Primary

MeasureTime frame
LIS score;No ventilator days;Coagulation;Indicators of inflammatory response;Indicators of lung injury;Biochemical Indicators;RASS score;APACHEII score;28-day mortality;SOFA score;Molecular biological marker lncRNA;

Countries

China

Contacts

Public ContactPeiyang Gao

Department of Critical Medicine, Affiliated Hospital of Chengdu University of traditional Chinese Medicine

1015527192@qq.com+86 18980025566

Outcome results

None listed

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