A Randomized Prospective Clinical Trial to Assess Procalcitonin-guidance and Molecular-guided Diagnosis as Mainstay for Therapy of Severe Infections (the MODIFY Trial)

Status: Recruiting
Location: See all (15) locations...
Intervention Type: Diagnostic test, Other
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

MODIFY is a randomized, open-labeled, and prospective study that will be conducted in multiple Intensive Care Units (ICUs) and departments of Internal Medicine across Greece. It aims to change the traditional approach for the management of severe infections by integrating the results of BCID2, Reveal Rapid AST, and PCT, to improve patients' outcomes. Early and precise identification of the underlying causative pathogen along with the fast acquisition of the antimicrobial sensitivity results may positively impact the uncontrolled antimicrobial prescription.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female

• For women of child-bearing potential, willingness to avoid pregnancy during the study and agreement to notify investigator if pregnancy occurs.

• Age more than or equal to 18 years

• Patients who have completed their participation in another study for more than 30 days can be included in this study.

• Written informed consent provided by the patient or by their legal representative in case of patients unable to consent due to sepsis onset affecting their mental capacity.

• Sepsis defined by the Sepsis-3 definition; this is defined separately for community-acquired sepsis and for hospital-acquired sepsis. Community-acquired sepsis is defined as any SOFA score 2 points or more for patients admitted in hospital emergencies with community-acquired pneumonia (CAP), community-acquired acute pyelonephritis (AP) or community-acquired primary bacteremia (BSI). CAP, AP and BSI are considered community-acquired for patients who have no history of hospitalization lasting more than 2 days the last 90 days or who are not under hemodialysis or who are not residents of long-term care facilities. Hospital-acquired sepsis is defined as any SOFA score increase by 2 points or more from the admission SOFA score for patients with onset of hospital-acquired pneumonia (HAP), ventilator-associated pneumonia (VAP), acute pyelonephritis (AP) or primary bacteremia (BSI) at least 48 hours after hospital admission. For patients with history of hospitalization lasting more than 2 days the last 90 days or who are under hemodialysis or who are residents of long-term care facilities and are admitted to hospital with HAP, VAP, AP and BSI the definition of hospital-acquired sepsis applies. In this case, the baseline SOFA score is considered as the known SOFA score before infection onset.

• Presence of one of the following infections: community-acquired pneumonia (CAP), hospital-acquired pneumonia (HAP), ventilator-associated pneumonia (VAP), acute pyelonephritis (AP) and primary bacteremia (BSI).

• Positive blood culture

Locations
Other Locations
Greece
2nd Department of Internal Medicine, University General Hospital of Alexandroupolis
NOT_YET_RECRUITING
Alexandroupoli
1st Department of Internal Medicine - General Hospital of Athens Sismanoglio- Amalia Fleming
NOT_YET_RECRUITING
Athens
1st Department of Internal Medicine- General Hospital of Athens GENNIMATAS
RECRUITING
Athens
1st Department of Internal Medicine, General Hospital of Athens KORGIALENIO-BENAKIO E.E.S.
RECRUITING
Athens
1st Department of Internal Medicine, General Hospital of Elefsina Thriasio
RECRUITING
Athens
2nd Propaedeutic Department of Internal Medicine, Attikon University Hospital
RECRUITING
Athens
3rd Department of Internal Medicine - General State Hospital of Nikaia Saint Panteleimon - West Attica General Hospital Agia Varvara
RECRUITING
Athens
3rd University Department of Internal Medicine, Sotiria Athens General Hospital
RECRUITING
Athens
4th Department of Internal Medicine, Attikon University Hospital
RECRUITING
Athens
Intensive Care Unit of Center for Respiratory Failure, Sotiria Chest Diseases Athens General Hospital
RECRUITING
Athens
New Multivalent Intensive Care Unit, Sotiria Chest Diseases Athens General Hospital
RECRUITING
Athens
Clinic of Intensive Care and Pulmonary Diseases, Aghioi Anargyroi Kifissia General Oncologic Hospital
RECRUITING
Kifissia
2nd Department of Internal Medicine, General Hospital of Piraeus Tzaneio
RECRUITING
Piraeus
1st University Department of Internal Medicine, AHEPA University General Hospital of Thessaloniki
NOT_YET_RECRUITING
Thessaloniki
Intensive Care Unit, Ippokrateion General Hospital
NOT_YET_RECRUITING
Thessaloniki
Contact Information
Primary
Evangelos Giamarellos-Bourboulis, MD,PhD
egiamarel@med.uoa.gr
00302105831994
Backup
Evdoxia Kyriazopoulou, MD, MSc, PhD
ekyri@med.uoa.gr
00302105832563
Time Frame
Start Date: 2023-09-19
Estimated Completion Date: 2026-12-27
Participants
Target number of participants: 190
Treatments
Sham_comparator: Standard-of-care
These patients will receive antibiotics according to standard practice of the attending physicians. The central lab will feedback to attending physicians and investigators the results of the conventional blood cultures and AST according to the routine SOP. The attending physicians and investigators will be allowed to decide for any change of antimicrobial treatment based on the results of conventional blood cultures provided to them by the central lab or any other culture provided to them by their hospital. Antibiotics will be stopped according to the local standard practice. BCID2, Reveal Rapid AST and PCT will be performed in the samples of these patients, attending physicians will not be provided such information.
Experimental: MODIFY strategy
These patients will start antibiotics according to standard practice of the attending physicians. It is anticipated that attending physicians will be informed in maximum 5 hours after randomization about the results of BCID2 including carriage of resistance genes and of the Reveal Rapid AST in the case of Gram-negative isolates. Physicians and investigators receiving this information are obliged to change the empirically prescribed antibiotics according to the rule provided in Box 1. The attending physicians and investigators will be allowed to decide for any change of antimicrobial treatment based on the results of conventional blood cultures provided to them by the central lab or any other culture provided to them by their hospital. PCT will be measured on day 1 and then daily starting from day 5. Attending physicians will be advised to discontinue antimicrobials on the first day by day 5 when PCT value is less than 80% of the initial value or it remains below 0.5 ng/ml.
Related Therapeutic Areas
Sponsors
Leads: Hellenic Institute for the Study of Sepsis

This content was sourced from clinicaltrials.gov