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A Study to See the Early Treatment and Bedside Ultrasound Help Patients with blood infection and complication of blood infection in the Emergency department of a Hospital in Manipur

A prospective observational Study evaluating the impact of combining the One-Hour Sepsis Bundle and Point-of-Care Ultrasound (POCUS) in Sepsis and Septic Shock Patients presenting to Emergency Department in a Tertiary Care Hospital, in Manipur - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/090571
Enrollment
110
Registered
2025-07-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: D758- Other specified diseases of bloodand blood-forming organs

Interventions

Intervention1: Nil: Nil

Sponsors

MUHAMMED SHADIL K E
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting to the ED with suspected sepsis or septic shock based on clinical criteria (e.g. qSOFA,NEWS2 score)

Exclusion criteria

Exclusion criteria: Patients (close relatives in case of unconscious patients) who refuse to give consent;Patients with age less than18 years and more than 65 years;Pregnant women;Known terminal illness with a prognosis of less than 6 months;Contraindications to ultrasound (e.g., extensive body surface area edema);Patients with spinal cord injury.

Design outcomes

Primary

MeasureTime frame
To evaluate the impact of combining the 1-hour sepsis bundle with POCUS on clinical outcomes (change in qSOFA, NEWS2, Lactate and Blood Pressure (MAP) ) in patients with sepsis or septic shock presenting to the Emergency Department.Timepoint: Period of one and half years from june 2025 to December 2026.—

Secondary

MeasureTime frame
1) To assess the time to intervention (antibiotics, fluids, vasopressors) in sepsis and septic shock patients. 2) To evaluate the accuracy and utility of POCUS in assessing volume status, cardiac function, and identifying potential sources of infection in septic patients. 3) To evaluate the effectiveness of POCUS in the prevention of fluid overload and to rule out differentials. 4) To evaluate change in qSOFA, NEWS2, serum lactate, and blood pressure (MAP) by combining the sepsis one-hour bundle and POCUS after one hour of identifying/ suspecting sepsis or septic shock.Timepoint: Period of one and half years from june 2025 to December 2026.—

Countries

India

Contacts

Public ContactMUHAMMED SHADIL K E

Shija Hospitals and Research Institute

khuraijam.sweta@gmail.com7982576807

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026