Terlipressin Infusion Alone Vs Terlipressin With Noradrenaline Infusion In The Treatment of Hepatorenal Syndrome Type 1

Type 1 HEPATO RENAL SYNDROME(HRS) Clinical Trial

Official title:

Comparison of The Effectiveness of Terlipressin Infusion Alone Vs Terlipressin With Noradrenaline Infusion In The Treatment of Hepatorenal Syndrome Type 1

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03822091
• Other study ID #: TERLI AND NORAD IN HRS
• Status: Completed
• Phase: Phase 3
• Start date: January 28, 2019
• Est. completion date: January 30, 2020

Study information

• Verified date: May 2023
• Source: Postgraduate Institute of Medical Education and Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Hepatorenal syndrome (HRS) is defined as a functional renal failure in a patient with chronic liver disease, or liver cirrhosis.The splanchnic circulation undergoes severe vasodilation, as a result of portal hypertension, causing an underfilling of systemic arteries.This results in intense renal vasoconstriction and functional renal failure. The best treatment options for HRS I would be a drug which has renal vasodilator property and additional splanchnic vasoconstriction. An increase in circulating blood volume would be of additional benefit. Currently Terlipressin is considered superior to other drugs in the management of HRS I. Other drugs in use are Noradrenaline and Midodrine. Albumin is added to these drugs in order to expand plasma volume. Terlipressin, a Vasopressin analog, has agonistic activity at V1 receptors. Noradrenaline acts as an agonist at α-adrenergic receptors with mild β-agonistic activity. The two major drugs used in the management of HRS act at different receptors and have completely varied mechanisms of action. Thus, a combination therapy would improve the rate of response considerably. There have been multiple studies, measuring the efficacy, safety and dosing of both drugs, but none combining both Terlipressin and Noradrenaline. Hence our study would be a pioneer in formulating a new and possibly more efficacious treatment protocol for patients of Type I HRS, in whom the treatment options are otherwise very limited. If successful, this would open new horizons of therapy for Terlipressin refractory HRS, which, otherwise is an ominous condition.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: January 30, 2020
• Est. primary completion date: January 30, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. age>18 years and <80 yrs;

2. Cirrhosis as diagnosed by clinical findings, endoscopy or USG examination or by liver biopsy.

3. HRS I as defined by the following features:

1. The patient should have Cirrhosis and also ascites

2. Renal failure of rapid onset -Initial value of sCr, doubling to reach a level of more than 226mmol/L (2.5 mg/dL) in less than two weeks

3. There should be absence of shock.

4. sCr value does not reduce to less than 1.5 mg/dl even after 2 days of stopping diuretics and giving Inj.Albumin for plasma volume expansion (1g/kg ) upto 100g/day.

5. No H/O being treated currently or recently with drugs having nephrotoxicity.

6. Absence of parenchymal renal disease:

• Proteinuria < 0.5g/day

• Absence of microhaematuria (<50 red cells/high powered field)

• Normal renal ultrasonography

Exclusion Criteria:

1. AKI improved after plasma volume expansion

2. Any history of coronary artery disease, peripheral vascular disease, arrhythmias, and cardiomyopathy.

3. Hepatocellular Carcinoma

4. Septic shock

5. Any severe extra-hepatic condition including respiratory and cardiac failure.

6. Any contraindication which precludes the use of Noradrenaline and Terlipressin

Related Conditions & MeSH terms

• Hepatorenal Syndrome
• Syndrome
• Type 1 HEPATO RENAL SYNDROME(HRS)

Intervention

Drug:
• Terlipressin
Patients with Type 1 HRS will be given Terlipressin at the dose of 2mg/24 hrs as infusion. After 48 hours of initial monitoring, patients who do not respond to the initial dose of Terlipressin, and randomised into group A and B. Group A patients will receive further higher doses of Terlipressin. The dose of Terlipressin will be increased by 1mg after 24 hrs if: the creatinine values decrease by <12.5% MAP increase of <10 mmHg urine output of <200 ml in 4 hours. Maximum terlipressin dose will be given upto 12 mg/day.Albumin will be administered in both arms according to standard protocol at the following dose : 1st day - Albumin at 1 gram/kg - a maximum dose of 100grams can be given. A dose of 20gram/day to 60gram/day in the following days.
• Terlipressin and Noradrenaline
Patients with Type 1 HRS will be given Terlipressin at the dose of 2mg/24 hrs as infusion. After 48 hours of initial monitoring, patients who do not respond to the initial dose of Terlipressin, will be randomised into group A and B. Group B patients will be treated with Terlipressin(2mg/24hr infusion- fixed dose) and Noradrenaline, which would be given as a continuous infusion at a starting dose of 0.5 mg/hr. The dose od noradrenaline will be increased every 24 hours in steps of 0.5 mg/hr, the maximum dose being 3 mg/hr IF: the creatinine values decrease by <12.5% MAP increase of <10 mmHg urine output of <200 ml in 4 hours.

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	Number of patients responding to treatment.	Complete response defined as serum creatinine <1.5 mg/dl	15 days
Secondary	Number of patients who will develop adverse events due to drugs used for treatment		15 days
Secondary	Number of patients surviving without transplant.		90 days