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Comparision between conventional blood coagulation tests vs Automated coagulation tests using Viscoelastic testing in patients suffering with infection/ sepsis.

Evaluation of automated viscoelastic point of care coagulation assay and Conventional tests of Coagulation and inflammatory markers in Sepsis- a prospective observational study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/04/051418
Enrollment
30
Registered
2023-04-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Health Condition 1: B949- Sequelae of unspecified infectiousand parasitic disease

Interventions

None listed

Sponsors

Armed forces Medical services research project
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients with sepsis admitted to the ICU

Exclusion criteria

Exclusion criteria: a. Age b. Consent not available c. Patients on therapeutic anticoagulation d. Patients with known chronic liver disease. e. Patients with primary hematological disorders. f. Patients in whom blood and blood products have been transfused within the past 48h. g. Patients on Vitamin K supplementation. h. Patients with pre-existing hypo or hypercalcemia. i. Patients with known congenital coagulation disorders. j. Patients who underwent surgery 07 days prior to enrollment. k. Pregnancy and peripartum period (up to 8 weeks post-delivery) l. Patients presenting with a primary diagnosis of trauma. m. Patients diagnosed with sepsis for more than 72h before enrolment/ admission to ICU.

Design outcomes

Secondary

MeasureTime frame
Need for blood and component transfusions.Timepoint: during the detection of any abnormal test results.

Primary

MeasureTime frame
The results of the conventional tests of coagulation and ROTEM/TEG will be interpreted as the presence or absence of abnormal coagulation. These rates will be compared using the appropriate statistical method.Timepoint: Three time phases of sepsis will be determined starting from the likely time of onset of sepsis less than 3 days 3 to7 days and more than 7 days.

Countries

India

Contacts

Public ContactKRISHNA KUMAR MYLAVARAPU

Army Hospital Research and Referral

krishnakm312@gmail.com9990457469

Outcome results

None listed

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