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Prospective Cohort Study of Huanglian Jiedu Decoction for Preventing Hospital-Acquired Infections in Intensive Care Unit Patients

Study on the Prevention and Treatment Effects of Huanglian Jiedu Decoction on Early Hospital-Acquired Infections in ICU Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026000096
Enrollment
Unknown
Registered
2026-01-17
Start date
2025-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

ICU acquired infection

Interventions

contrast group:According to the International Guidelines for the Campaign to Save Sepsis (2023 Edition), standard treatments such as anti infection, fluid resuscitation, and organ function support sho
Medication group:On the basis of routine standardized treatment, Huanglian Jiedu Tang is used as an adjuvant therapy(The medication includes 9g Huanglian, 6g Huangqin, 20g Huangqi, 9g Jiaozi, 10g Cinn

Sponsors

Lanzhou University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Severe patients diagnosed with sepsis who meet the diagnostic criteria for sepsis; (2) Age = 18 years old; (3) Patients who meet the criteria of traditional Chinese medicine and are willing to receive treatment with Huanglian Jiedu Tang and sign an informed consent form; (4) No MDROs were detected in microbial culture upon enrollment (or no evidence of MDROs colonization upon admission).

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women; (2) Patients with severe multiple organ failure, tumor cachexia, or organ transplantation combined with long-term use of immunosuppressants, as well as those with an expected survival period of less than 3 months; (3) Individuals who are allergic or intolerant to the ingredients of Huanglian Jiedu Decoction; (4) Patients who have recently been hospitalized in other hospitals and are also infected with MDROs within the hospital; (5) Those who are currently participating in other clinical trials or have completed clinical trials of other drugs for less than 3 months.

Design outcomes

Primary

MeasureTime frame
Incidence of hospital acquired infections;

Secondary

MeasureTime frame
28-day all-cause mortality;ICU length of stay;Total hospital length of stay;Duration of mechanical ventilation;Changes in inflammatory markers (CRP, PCT, IL-6);Changes in Sequential Organ Failure Assessment (SOFA) score;Incidence of adverse events;

Countries

China

Contacts

Public ContactLiping Liu

Lanzhou University First Hospital

liulipingldyy@126.com18993189155

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026