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delta lactate for monitoring liver graft function in post liver transplantations patients

utility of delta lactate for predicting early allograft dysfunction in adult patients undergoing liver transplantations- A prospective observational study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/11/076244
Enrollment
50
Registered
2024-11-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: K77- Liver disorders in diseases classified elsewhere

Interventions

Intervention1: nil: nil Control Intervention1: Nil: Nil

Sponsors

Department of Liver anaesthesia and critical care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients aged between 18-65 years who are undergoing living donor liver transplantation at our institution.

Exclusion criteria

Exclusion criteria: Age less than 18 years Patient refusal Diagnosed with infections like Empyema, spontaneous bacterial peritonitis intra-operatively AKI within 7 days prior to transplant, in the preoperative period Patient posted for re-exploration/surgery within POD 2. Patient on CRRT – intra op and post operative

Design outcomes

Primary

MeasureTime frame
To evaluate the change in lactate over 12 hours (delta lactate 0-12) as an early marker for early allograft dysfunction in Living donor liver transplant recipient (LDLTR) in early post-op periodTimepoint: 8 weeks

Secondary

MeasureTime frame
To evaluate the change in lactate over 6 hours (delta lactate 0-6) and 24 hours (delta lactate 0-24) as markers for early allograft dysfunction in LDLTR in the early postoperative period. To examine the association between delta lactate levels and postoperative incidence of sepsis, AKI, prolonged mechanical ventilation, and biliary complications. To examine the association between delta lactate levels and length of hospital stay, ICU stay, and 30-day and 90-day mortality ratesTimepoint: from POD - 0 to discharge from hospital, with 30 day and 90 day mortality

Countries

India

Contacts

Public ContactElavarasan

Dr Rela institute and medical center

Akila.Rajakumar@relainstitute.com9840136295

Outcome results

None listed

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