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THE IMMUNOLOGICAL EFFECTS AND METABOLIC TOLERANCE OF LIPID INFUSION IN PATIENTS WITH CIRRHOSIS.

THE IMMUNOLOGICAL EFFECTS AND METABOLIC TOLERANCE OF LIPID INFUSION IN PATIENTS WITH CIRRHOSIS.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02381769
Enrollment
55
Registered
2015-03-06
Start date
2013-06-30
Completion date
2014-12-31
Last updated
2016-09-12

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

Conditions

Alcoholic Liver Disease

Brief summary

The study will be an experimental pre-post trial in which patients with ethanol related liver disease (both severe alcoholic hepatitis and decompensated ) admitted in our institute from Jun 2013-Dec 2014 will be enrolled in the study. Those on ryle's tube feeding would receive polymeric blenderized kitchen based liquid diet while those tolerating orally would receive soft/ solid diet as tolerated as per requirement. All the patients would receive same amount of calories i.e., 30-35 kcal/kg ideal body weight/ day and 1-1.2 gm/kg protein. 35-40% of non protein calorie would be provided as fats and rest of the calories will be provided as carbohydrates. All patients will be transfused 250ml of 20% intra lipid per day for 3 consecutive days, over and above the feed provided to them to be taken enterally (orally or through Ryle's Tube). Patients will undergo tests prior to infusion and 72 hours after infusion.

Interventions

DIETARY_SUPPLEMENTSoybean based lipid emulsion

Sponsors

Institute of Liver and Biliary Sciences, India
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

'Inclusion Criteria: * Subjects aged ≥ 18 years. * Patients with alcohol related liver disease (severe alcoholic hepatitis and decompensated cirrhosis) * Patients tolerating enteral nutrition.

Exclusion criteria

* Active ongoing Gastrointestinal bleed. * Unresolved sepsis * Allergy to soya oil, eggs, peanuts or other ingredients of intralipid. * Co-morbidities like Diabetes mellitus, hyperlipidemia, Coronary Artery Disease (CAD) and hypothyroidism. * Renal failure (S.creatinine \> 1.5mg %) * Pregnancy * Patients on high inotropic support (requiring more than 1 inotropic support) * Refusal to participate in the study

Design outcomes

Primary

MeasureTime frame
Effect of intravenous lipid on monocytes counts.3 days
Effect of intravenous lipid on neutrophils counts.3 days
Effect of intravenous lipid on macrophages count.3 days

Secondary

MeasureTime frame
Influence of lipid infusion on TEG (Thromboelastography)3 days
Influence of lipid infusion on TNF-α (Tumor Necrosis Factor).3 days
Influence of lipid infusion on interleukin levels (IL-6, IL-10).3 days
Influence of lipid infusion on PT/INR3 days
Influence of lipid infusion on renal parameters.3 days
Influence of lipid infusion on arterial ammonia.3 days
Influence of lipid infusion on PTT.3 days
Influence of lipid infusion on liver parameters.3 days

Other

MeasureTime frameDescription
Influence of lipid infusion on nitrogen balance3 daysnitrogen balance would be calculated by 24 hours urinary blood urea nitrogen estimation.
Metabolic tolerance of lipid infusion.3 daysMetabolic tolerance would be assessed by effect on serum triglycerides level ,serum free fatty acid level,arterial lactate level.
Effect of lipid infusion on Oxidative stress.3 daysOxidative stress would be determine by using urinary isoprostane test.

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026