Institute of Liver & Biliary Sciences
New Delhi, National Capital Territory of Delhi, 110070, India
NCT Number: NCT05767229
Clinically significant portal hypertension (CSPH) is defined as Hepatic Venous Pressure gradient (HVPG) >10 mmHg. Patients with CSPH are at risk of developing esophageal varices and clinical decompensation (variceal bleeding, ascites, jaundice, encephalopathy), which mark the transition from compensated stage to a stage of the disease (decompensated) associated with higher mortality. HVPG is calculated by subtracting the free hepatic venous pressure (FHVP), a measure of systemic pressure, from the wedged hepatic venous pressure (WHVP), a measure of hepatic sinusoidal pressure. HVPG is surrogate marker in many clinical applications such as gold standard test to evaluate presence and severity of portal hypertension (PHT) diagnosis, risk stratification, monitoring of the patients on beta blockers. Non-selective beta-blockers like propranolol and carvedilol are indicated in adults for primary and secondary prophylaxis of variceal hemorrhage. Acute hemodynamic response to intravenous propranolol with HVPG values coming down to < 12 mm Hg or reduction to >20% from baseline have been shown to be associated with reduced long-term risk of variceal bleed. Portal Hypertension in biliary atresia (BA) occurs early and is due to recurrent cholangitis and portal sclerosis. HVPG in children is feasible and safe in children according to previous studies, however, there are no recommendations to suggest beta-blockers based on HVPG reduction in children. Hence, we are planning the current work to study the acute hemodynamic response to carvedilol in children with CSPH, and to compare the HVPG values in children with chronic liver disease.
Looking for future studies?
Notify Me2 year–18 year
All sexes
Interventional
Not applicable
New Delhi, National Capital Territory of Delhi, 110070, India
Aim: To study acute hemodynamic response Hepatic Venous Pressure Gradient (HVPG) reduction to <12 mm Hg or by ≥ 20% from initial value) to carvedilol in from 2 to 18 year of age children with Chronic liver disease.
Methodology Study population: All children (2-18) years of age with CLD as per inclusion and exclusion criteria
Study design: Prospective cohort
Baseline parameters that will be recorded:
Study period: 2 years
Sample size with justification: Since it is a pilot study we will take 40 patients
Methodology for HVPG measurement:
Acute Hemodynamic response to oral carvedilol:
Monitoring and Assessment:
Statistical Analysis All the categorical variables will be expressed as frequencies, whereas continuous ones will be expressed as mean+ SD or median (IQR). Chi-square , Fisher's exact test and student's t-test will be applied for assessment of causality. Kaplan-Meier statistics will be done for survival and liver related morbidity besides this an appropriate analysis will be carried out at the time of data analysis like diagnostic test, logistic regression etc. Significance will be mentioned in the form of p-value <0.05.
Adverse effects:
Stopping rule of study:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Carvedilol 0.2 mg/kg for 1.5 hrs
Time frame: 90 minutes
Acute hemodynamic response (HVPG reduction to less than 12 mm Hg or by more than equals to 20% from initial value
Time frame: Day 0
Time frame: Day 0
Time frame: Day 0
Time frame: Day 0
Time frame: Day 0
Time frame: Day 0
Time frame: 6 months
Institute of Liver and Biliary Sciences, India
Other
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