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An observational study to assess the blood clotting disorders on patients admitted in intensive care unit.

An observational study on assessment of coagulation abnormalities in critically ill patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091005
Enrollment
108
Registered
2025-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: D65- Disseminated intravascular coagulation [defibrination syndrome]

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Sri Ramachandra Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Invasive procedure and Significant trauma

Exclusion criteria

Exclusion criteria: Patients with known stable chronic thrombocytopenia and patients with isolated vitamin K deficiency

Design outcomes

Primary

MeasureTime frame
Mortality in ICU patients.Timepoint: 4 weeks—

Secondary

MeasureTime frame
Need for interventions based on the abnormality.Timepoint: 4 weeks—

Countries

India

Contacts

Public ContactDR Baby Sailaja K

Sri ramachandra institute of higher education and research

sailajaroop@gmail.com9600159482

Outcome results

None listed

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