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comparison of reliability of point of care testing with conventional laboratory testing for coagulation profile in adult trauma patients.

Correlation of point of care with conventional laboratory testing for coagulation profile in adult trauma patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/03/024378
Enrollment
60
Registered
2020-03-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: T07- Unspecified multiple injuries

Interventions

None listed

Sponsors

Vardhman Mahavir Medical College and Safdarjung Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients coming to the emergency department with one or more of the following injuries: Traumatic brain injury with a GLASGOW COMA SCORE <13,Chest trauma, Abdominal injury, Pelvic fracture or long bone fractures.

Exclusion criteria

Exclusion criteria: 1.Pregnant patient 2.known case of haemorrhagic and hepatic disorders 3.patients on anticoagulants and antiplatelets 4.Prior blood transfusion in the last 72 hours

Design outcomes

Primary

MeasureTime frame
To study the correlation of point of care with conventional laboratory testing for coagulation profile (prothrombin time / international normalized ratio) in adult trauma patients coming to the emergency department ,using PEARSON or SPEARMAN correlation coefficient.Timepoint: 1.At the time of insertion of I.V canula and sample collection 2.After fluid resuscitation with one litre of warm crystalloids—

Secondary

MeasureTime frame
To evaluate the sensitivity and specificity of point of care coagulation profile (prothrombin time / international normalized ratio),assuming conventional laboratory coagulation profile (prothrombin time / international normalized ratio) as the gold standard, in adult trauma patients coming to the emergency department.Parameters which will be used in this study are PT & INR of both POCT(ABBOT i-STAT) and conventional laboratory testing.Timepoint: 1.At the time of insertion of I.V canula and sample collection 2.After fluid resuscitation with one litre of warm crystalloids—

Countries

India

Contacts

Public ContactJayaram S

Vardhman Mahavir Medical College and Safdarjung Hospital

nikkisabharwal162@gmail.com9810774396

Outcome results

None listed

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