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Blood Sugar and White Blood Cell Ratio to Predict Outcome in Sepsis Patients

Glucose and Lymphocyte Ratio as a Prognostic Marker In Patients of Sepsis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/082129
Enrollment
115
Registered
2025-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: D899- Disorder involving the immune mechanism, unspecified

Interventions

Control Intervention1: NIL: NIL

Sponsors

Datta Meghe Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with sepsis: Only individuals who meet the clinical criteria for sepsis (e.g., infection with systemic inflammatory response) should be included in the study. 2.Adults aged 18 years and above: Include adult patients, as the study may focus on how glucose and lymphocyte ratios impact prognosis in the adult population. 3.Availability of relevant laboratory data: Participants should have recent blood tests, including glucose levels and lymphocyte counts, available for analysis to calculate the glucose and lymphocyte ratio.

Exclusion criteria

Exclusion criteria: 1.Diabetic patients Pre-existing diabetes alters glucose levels affecting study outcomes. 2.Immunosuppressed patients Those on chemotherapy, steroids, or immunosuppressants may have skewed lymphocyte ratios. 3.Hematologic or autoimmune disorders Conditions like leukemia or lupus impact lymphocyte counts introducing bias.

Design outcomes

Primary

MeasureTime frame
1.Mortality rate 28-day in-hospital mortality. 2.ICU length of stay Duration of ICU admission. 3.Organ dysfunction progression Evaluated using SOFA score changes.Timepoint: 1.Mortality rate 28-day in-hospital mortality. 2.ICU length of stay Duration of ICU admission. 3.Organ dysfunction progression Evaluated using SOFA score changes.

Secondary

MeasureTime frame
1.Need for mechanical ventilation Incidence and duration of ventilatory support. 2.Vasopressor requirement Need and duration of vasopressor therapy. 3.Septic shock development Progression from sepsis to septic shock. 4.Hospital length of stay Total duration of hospitalization. 5.Inflammatory markers Trends in CRP and procalcitonin levels.Timepoint: 1.At admission (Day 0) Baseline assessment. 2.Day 3 & Day 7 Follow-up evaluation of progression. 3.Day 14 Intermediate outcome assessment. 4.Day 28 Final outcome evaluation.

Countries

India

Contacts

Public ContactDr Jaswanth Varma Alluri

Datta Meghe Institute of Higher education and Research

tushar.ihmp@gmail.com7820858332

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026