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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03420144
Other study ID # GH in cirrhosis
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date January 15, 2018
Est. completion date June 30, 2020

Study information

Verified date April 2023
Source Postgraduate Institute of Medical Education and Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Liver cirrhosis (LC) is a leading cause of morbidity and mortality worldwide. Life- threatening complications of liver cirrhosis are ascites, gastrointestinal bleeding, variceal bleed, hepatic encephalopathy and hepatocellular carcinoma (HCC) which are associated with poor prognosis.The leading causes of liver cirrhosis include excess alcohol consumption, viral hepatitis and non-alcoholic fatty liver disease. Malnutrition is common in end-stage liver disease (cirrhosis) and is often associated with a poor prognosis. It occurs in all forms of cirrhosis with different etiology and prevalence ranges from 65 to 100% depending upon the methods used for nutritional assessment and the severity of liver disease. Nutritional state influences survival in patients with decompensated cirrhosis. Protein malnutrition manifested by reduced skeletal muscle mass and hypoalbuminemia, exist in patients with cirrhosis despite apparent adequate food consumption and these patients have a higher rate of complications and, overall, an increased mortality rate. Also, Malnutrition has significant implications for liver transplantationÍž patients with poor nutritional status before transplantation have increased complications and higher mortality rates postoperatively. Screening all patients with chronic liver disease for nutritional abnormalities can identify those at risk of developing preventable complications. Malnutrition is commonly associated with protein catabolism and the protein catabolic state of cirrhosis is associated with severe growth hormone (GH) resistance, with low levels of insulin-like growth factor (IGF)-I and its major binding protein (IGFBP)-3. GH therapy in cirrhosis has been shown to improve nitrogen economy and to improve the GH resistance in a small pilot study by Donaghy et al. Also, GH therapy of short duration has shown to increase IGF1 levels, IGFBP-3 levels in patients of cirrhosis. GH therapy has also shown to improve liver regeneration and protein synthesis after hepatectomy in patients of HCC with cirrhosis. However there is scarcity of data on clinical impact of long term administration of GH therapy in patients of cirrhosis. Hence, we undertook the present study to study the effect of growth hormone on nitrogen economy, malnutrition and liver regeneration in patients with cirrhosis.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date June 30, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Decompensated Cirrhosis of liver irrespective of etiology Exclusion Criteria: - Acute on chronic liver failure (fulfilling either APASL or CANONIC criteria of ACLF) - Splenic diameter of more than 18 cm - Concomitant HCC or other active malignancy - Upper gastrointestinal bleeding in the previous 7 days - Portal vein thrombosis - Severe renal dysfunction as defined by creatnine > 1.5mg/dl - Severe cardiac dysfunction - Uncontrolled diabetes (Hb A 1c = 9) or diabetic retinopathy - Acute infection or disseminate intravascular coagulation - Active alcohol abuse in last 3 months - Known hypersensitivity to GH - HIV co-infection - Pregnancy - Refusal to give informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Standard Medical Therapy
Standard Medical Therapy will include nutritional support, rifaximin, lactulose, bowel wash, albumin, diuretics, multivitamins and antibiotics as required
Growth Hormone
GH therapy is initiated at a low dose of 1U/day and titrated slowly upward to a maximum dose of 3U/day (depending on IGF-1 levels) subcutaneously for 1 year.

Locations

Country Name City State
India Post Graduate Institute of Medical Education and Research Chandigarh

Sponsors (1)

Lead Sponsor Collaborator
Postgraduate Institute of Medical Education and Research

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in Nutritional status based on CT L3 SMI score. Nutritional status will be assesses by skeletal muscle index measurement using CT scan measurements at L3 level One year
Secondary Improvement in BMI One Year
Secondary Improvement in Mid arm muscle circumference(MAMC) One year
Secondary Improvement in hand grip strength Hand grip strength will be measured with the hydraulic hand dyanamometer in Kg/force. One year
Secondary Clinical improvement in liver function Occurrence of decompensations namely ascites, hepatic encephalopathy and variceal bleed One Year
Secondary Biochemical improvement in liver function Improvment in MELD score One year
Secondary Improvement in Quality of life Quality of life will be assessed using SF-36V2 Health Survey questionnaire One Year
Secondary Improvement in liver regeneration By measuring hepatic parenchymal cell specific marker (CD 133) and cell proliferation marker (Ki-67) by immunohistochemistry. One Year
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