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Clinical Trials in Spain / NCT05783661
Recruiting Phase 4

Trial Comparing Conventional Antibiotic Strategies Versus Regimens Guided by Epidemiological Surveillance in Infected Patients With Cirrhosis (SURVIC_STUDY)

NCT05783661 · tracked via the Priya Life Science Spain tracker
Sponsor
Eva Bonfill
Phase
Phase 4
Started
2023-12-11
Last updated
2026-07-07

Condition(s) studied

Decompensated CirrhosisBacterial Infections

Investigational drug(s) / intervention(s)

Conventional antibiotic strategiesRegimens guided by epidemiological surveillance

Conventional antibiotic strategies: Treatment according to the local guidelines of the Hospital Clinic de Barcelona.

Regimens guided by epidemiological surveillance: Treatment according to the local guidelines of the Hospital Clinic de Barcelona guided by colonization/epidemiological surveillance.

Study summary

Study to comparing conventrional antibiotic strategies versus regimens guided by epidemiological surveillance in infected patients with cirrhosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Cirrhotic patients with acute decompensation aged ≥18 years. 2. Proven or suspected bacterial infection requiring antibiotic therapy (diagnosis will be established according to local guidelines, Appendix 1). 3. Signed informed consent or consent given by their legal representatives or close relatives. Exclusion Criteria: 1. Bacterial infection lasting for \> 48 hours. 2. Infection in a critically ill cirrhotic patient (ICU admission). In this population, epidemiological surveillance is standard clinical practice. 3. MDR colonization or infection in the last month. 4. Evidence of current locally advanced or metastatic malignancy (patients with hepatocellular carcinoma within the Milan criteria and non-melanocytic skin cancer can be included). 5. Pregnant and/or breast-feeding woman. 6. Patients who cannot provide prior informed consent and when there is documented evidence that the patient has no legal surrogate decision-maker and it appears unlikely that the patient will regain consciousness or sufficient ability to provide delayed informed consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Eva Bonfill Barcelona Spain Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05783661 on ClinicalTrials.gov ↗ ← All trials in Spain