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Construction of a Database for the Life-cycle Sepsis-specific Disease Cohort

Construction of a Database for the Life-cycle Sepsis-specific Disease Cohort

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04872010
Enrollment
4000
Registered
2021-05-04
Start date
2021-06-01
Completion date
2022-09-30
Last updated
2021-05-04

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

Conditions

Sepsis

Brief summary

Establish a structured clinical database for sepsis screening, and establish a special data set standard for sepsis throughout the life cycle.

Interventions

None listed

Sponsors

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients with sepsis who meet the Sepsis 3.0 standard proposed by the 2016 International Sepsis Expert Consensus, that is, for patients with infection or suspected infection, when sepsis-related sequential organ failure (Sequential (Sepsis-related) Organ Failure) Assessment (SOFA) score increased by ≥ 2 points from the baseline can be diagnosed as sepsis; 2. It is estimated that the patient's ICU stay ≥24 hours; 3. Obtain informed consent and sign an informed consent form.

Exclusion criteria

1. The patient's ICU hospital stay is less than 24 hours; 2. Participated in other clinical research; 3. Failed to sign the informed consent form.

Design outcomes

Primary

MeasureTime frameDescription
Sepsis organ function status and survival analysis.2022.09.30Safety indicators include: prognosis: mortality, intensive care unit (ICU) treatment time and hospital stay, incidence of nosocomial infections, treatment-related complications.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026