Skip to content

A multicenter, randomized, parallel controlled study of golden 3-hour cluster intervention strategy in emergency patients with septic shock

A multicenter, randomized, parallel controlled study of golden 3-hour cluster intervention strategy in emergency patients with septic shock

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037266
Enrollment
Unknown
Registered
2020-08-27
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-10-13

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

Conditions

Septic shock

Interventions

experimental group:The detailed golden 3 hours cluster intervention strategy
control group:Gold 3-hour cluster intervention strategy recommended by 2016 sepsis 3.0

Sponsors

Huashan Notth Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.The patient with septic shock meeting Sepsis3.0 clinical diagnostic criteria; 2. Aged 18 ~70 years; 3. Chinese males and non-pregnant females; 4. Initial case of acute septic shock; 5. Understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Intravenous use of antibiotics before emergency treatment; 2. Cases of septic shock that occurred 24 hours after admission to the emergency department; 3. Cases referred from other hospitals; 4. Cases of advanced cancer and the terminal and irreversible deathbed state of various diseases; 5. Cases of drug abuse; 6. Patients who are currently receiving glucocorticoids or other immunosuppressive or immunomodulatory agents within the first 3 months of initiation; 7. Patients who participated in other clinical studies within 3 months before this study.

Design outcomes

Primary

MeasureTime frame
hemodynamics;infection markers;severity score;medical expenses;prognostic;

Countries

China

Contacts

Public ContactZhijie Xia

Huashan North Hospital, Fudan University

janexia2006@126.com+86 18121186337

Outcome results

None listed

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