Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:52 PM
Ignite Modification Date:
2025-12-24 @ 3:52 PM
NCT ID:
NCT02217592
Eligibility Criteria:
Inclusion Criteria:
* Males and females 18 years old
* Thai nationality
* Required hospitalization as decided by the attending physician
* Documented by attending physician that an infection is the primary cause of illness leading to the hospitalization. These can be infections due to any pathogens (bacteria, viruses, fungi and parasites)
* Presence of any 3 of the following Systemic Inflammatory Response Syndrome (SIRS)
* Fever or hypothermia (Core body temperature defined as \> 38.3 C or \< 36.0 C)
* Tachycardia (heart rate \> 90 beats per minute)
* Tachypnea (respiratory rate \> 20 per minute)
* Arterial hypotension (systolic blood pressure (SBP) \< 90 mmHg, mean arterial pressure (MAP) \< 70 mmHg, or SBP decrease \> 40 mmHg)
* White blood cell (WBC) \> 12,000/µL \< 4000/µL or immature forms \> 10%
* Platelet count \< 100,000/microlitre
* Altered mental status with Glasgow Coma Score (GCS) \< 15
* Hypoxemia (Pulse Oximetry Level \< 95)
* Ileus
* Significant edema or positive fluid balance
* Decreased capillary refill or mottling
* Hyperglycemia (plasma glucose \> 140 mg/dL) in the absence of diabetes
* Plasma C-reactive protein \> 2 SD above the normal value
* Plasma procalcitonin \> 2 SD above the normal value
* Arterial hypoxemia (PaO2 / FIO2 \< 300)
* Acute oliguria (urine output \< 0.5 mL/kg/hr or 45 mmol/L for 2 hours)
* Creatinine increase \> 0.5 mg/dL
* INR \> 1.5 or aPTT \> 60 seconds
* Plasma total bilirubin \> 4 mg/dl or 70 mmol/L
* Hyperlactatemia (\> 1 mmol/L)
Exclusion Criteria
* Infection is not suspected to be a primary cause of the current illness episode leading to the hospitalization. For example, community-acquired sepsis or severe sepsis is considered to be due to stroke, cardiovascular diseases, acute myocardial infarction, cancer, burn, injury, and trauma
* Hospitalized at this study site for this current episode for more than 24 hours before enrollment
* Hospitalized for this current episode for more than 72 hours at another primary/referring hospital
* Prior to this current episode, the patient was admitted to any hospital within the last 30 days
* Prior to enrolment, it is documented by the attending physician that hospital acquired infection is associated with the cause of sepsis or severe sepsis
Please note that the following conditions are not exclusion criteria, and patients with the following conditions can be enrolled into the study
* Confirmed diagnosis by any method of an infection as a major cause of illnesses leading to hospitalization. For example, a patient who already has had a definite diagnosis of malarial infection by blood smear
* Clinical diagnosis of any specific disease or any specific syndromes such as acute infective diarrhea, acute pneumonia, acute encephalomyelitis and acute myocarditis
* Suspected of having both infectious and non-infectious diseases and infectious disease is a primary cause of illnesses (primary diagnosis) leading to the hospitalization. For example, acute pneumonia with stroke as an underlying disease, etc
* Patients who are admitted to other hospitals and referred to the study site. For example a referred patient who admit to the first hospital less than 48 hours prior to enrollment
* Patients fulfilling the inclusion criteria without having result of complete blood count or result of all parameters in the inclusion criteria. For example, a patient who has hypothermia, tachycardia and tachypnea completes the criteria of SIRS even without the result of complete blood count or the result of other parameters such as INR, or plasma procalcitonin
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02217592
Study Brief:
Protocol Section:
NCT02217592