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Correlation of laboratory based tests(PT, APTT, Fibrinogen, Platelets) and point of care tests(Thromboelastography) during different stages of living donor liver transplant surgery

An observational study of haemostatic profile during different stages of liver transplant surgery using laboratory based tests and thromboelastography - HOLT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/06/014568
Enrollment
20
Registered
2018-06-18
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: K745- Biliary cirrhosis, unspecified Health Condition 2: null- LIVER TRANSPLANT RECIPIENT

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

ARTEMIS HEALTH INSTITUTE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: RECIPIENT OF LIVER TRANSPLANT SURGERY

Exclusion criteria

Exclusion criteria: ALL EXCLUSION CRITERIA FOR LIVER TRANSPLANT SURGERY LIKE: EXTRAHEPATIC MALIGNANCY ACTIVE SUBSTANCE ABUSE ACTIVE EXTRAHEPATIC INFECTIONS

Design outcomes

Primary

MeasureTime frame
PT, APTT, PLATELET COUNT, FIBRINOGEN, THROMBOELASTOGRAPHY READINGSTimepoint: AT INDUCTION OF ANAESTHESIA, 2 HOURS INTO PRE ANHEPATIC PHASE, HALF HOUR INTO ANHEPATIC PHASE, HALF HOUR INTO REPERFUSION PHASE, AT CLOSURE OF SURGERY, 12 POST OPERATIVE, 24 HOURS POST OPERATIVE—

Secondary

MeasureTime frame
TRANSFUSION OF BLOOD AND BLOOD PRODUCTSTimepoint: INTRAOPERATIVELY—

Countries

India

Contacts

Public ContactSHWETA BANSAL

ARTEMIS HEALTH INSTITUTE

amitkhatuja83@gmail.com9958017766

Outcome results

None listed

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