Skip to content

Comparing the blood test values In critically infectious patients.

Comparing the diagnostic accuracy of Mid regional Proadrenomedullin with Procalcitonin as a biomarker of sepsis in critically ill patients: A Prospective Observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/07/070897
Enrollment
84
Registered
2024-07-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: R99- Ill-defined and unknown cause of mortality

Interventions

Intervention1: Nil: Nil

Sponsors

All India Institute of Medical sciences, Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged above 18 years 2. Patients having clinical features suggestive of sepsis as defined by Sepsis-3 definition (2016) at the time of ICU admission

Exclusion criteria

Exclusion criteria: 1. The patient/relatives who refused to give Informed consent 2. Age less than 18 years 3. Patients with terminal stage of disease (malignant cancer of any type, acquired immunodeficiency syndrome, end-stage liver or renal disease). 4. HIV/HBsAg/HCV 5. Autoimmune disorders/Metabolic diseases 6. On long term steroids/ Immunosuppressants/ Chemotherapy 7. Osteoarthritis.

Design outcomes

Primary

MeasureTime frame
The primary objective is to compare the diagnostic accuracy of mid regional Proadrenomedullin with procalcitonin for diagnosis of sepsis in Critically Ill patients.Timepoint: Day 0 and at day 7 or day of death or discharge whichever is earlier.

Secondary

MeasureTime frame
To evaluate the ability of Proadrenomedullin to prognosticate the multi organ failure in critically ill sepsis patients as assessed by SOFA scores. To establish Proadrenomedullin as a predictor of outcome of sepsis in terms of 28 days mortality. To compare Proadrenomedullin, procalcitonin values as a prognostic marker of sepsis. Timepoint: Follow up for 7 days or till date of death.

Countries

India

Contacts

Public ContactDR Malarvizhi E

Department of Anaesthesiology and Critical care, AIIMS Jodhpur

drnikhilkothari@gmail.com8003996948

Outcome results

None listed

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