To Develop and Validate an Equation for Determination of Major Adverse Kidney Events in Patients With Decompensated Cirrhosis and Ascites.
NCT07794787 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 400
Last updated 2026-08-31
Summary
Acute kidney injury (AKI) is the sudden loss of kidney function that occurs frequently in hospitalised patients with cirrhosis.
* It develops in up to 53% and is independently associated with high short-term mortality.
* A diagnosis of AKI (even stage 1 AKI) has been shown to be associated with an increased risk of long-term mortality at 30-day, 90-day and 1-year, compared to patients without AKI, even when there is recovery of AKI.
* Risk factors with the strongest association for developing AKI include CKD, sepsis, spontaneous bacterial peritonitis (SBP), and presence of ascites.
* AKI in cirrhosis is also associated with development of de-novo chronic kidney disease (CKD) , progressive loss of kidney function in patients with pre-existing CKD,recurrent AKI (i.e., AKI on top of CKD) and other organ failures
* Kidney dysfunction in patients with cirrhosis is associated with a marked increase in mortality compared with patients without kidney dysfunction.
* The accurate estimation of kidney function in patients with cirrhosis is hence crucial for prognosis, treatment strategies, and decisions regarding simultaneous liver-kidney transplantation (SLKT).
* Although measured GFR(mGFR) may be ideal for assessing kidney function, it is costly, time-consuming, and challenging to perform frequently in fluctuating kidney function. Therefore, GFR is most commonly estimated using serum creatinine (sCr)-based or cystatin C (CysC)-based equations
Conditions
- Decompensated Cirrhosis
Sponsors & Collaborators
-
Institute of Liver and Biliary Sciences, India
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-08-31
- Primary Completion
- 2026-12-31
- Completion
- 2026-12-31
Countries
- India
Study Locations
More Related Trials
-
To Study and Compare the Clinical Course and Development of Organ Failure in Severe Acute Hepatitis Without Ascites, Non-cirrhotic and Cirrhotic Patients With Ascites [Acute on Chronic Liver Failure] and Acute Deterioration of Previously Decompensated Cirrhosis.
NCT02465619 ·Status: WITHDRAWN
-
To Study Efficacy of Albumin in Cirrhosis With Spontaneous Bacterial Peritonitis at Low Risk for AKI Development
NCT04437810 ·Status: UNKNOWN ·Phase: NA
-
Albumin Infusion in Inpatients With Decompensated Cirrhosis
NCT05719051 ·Status: UNKNOWN
-
Evaluation of Low-dose Albumin and Midodrine Versus Midodrine Alone in Outcome of Recurrent Ascites in Patients With Decompensated Cirrhosis.
NCT06245590 ·Status: UNKNOWN ·Phase: NA
-
To Study the Influence of GCSF on Natural History of Acute On Chronic Liver Failure After the Acute Phase
NCT02788240 ·Status: TERMINATED ·Phase: NA
-
To Compare the Efficacy of Nor Adrenaline and Terlipressin vs Step up Terlipressin Therapy in Hepatorenal Syndrome
NCT01649037 ·Status: WITHDRAWN ·Phase: NA
-
Evaluation of Mechanisms Responsible for Coma in Patients Affected by Fulminant, Acute and Chronic Hepatic Failure
NCT01582087 ·Status: TERMINATED
-
The Impact of Transjugular Intrahepatic Portosystemic Shunt on Recompensation in Patients With Decompensated Liver Cirrhosis
NCT07172035 ·Status: RECRUITING
-
Acute hemodynamiC Response To Carvedilol Predicts Survival in ACLF Patients
NCT06298656 ·Status: NOT_YET_RECRUITING
-
Early TIPS in Patients With Liver Cirrhosis and Ascites
NCT06576934 ·Status: RECRUITING ·Phase: NA
-
Evaluation of the Role of Plasma Biomarkers in the Development of Decompensation in Patients With Cirrhosis .
NCT03084185 ·Status: UNKNOWN
-
A Study of OCE-205 in Participants With Cirrhosis With Ascites Who Developed Hepatorenal Syndrome-Acute Kidney Injury
NCT05309200 ·Status: COMPLETED ·Phase: PHASE2
-
NEPH-ROSIS (NEPHrology in CirRhOSIS) Pilot Trial: A Trial to Treat Acute Kidney Injury Among Hospitalized Cirrhosis Patients
NCT06000748 ·Status: TERMINATED ·Phase: PHASE2/PHASE3
-
Gastric Antral Vascular Ectasia in Patients With Cirrhosis: Risk-factors and Associations.
NCT05690750 ·Status: UNKNOWN
-
Evaluation of Albumin and Midodrine Versus Albumin Alone in Outcome of Refractory Ascites in Patients With Decompensated Cirrhosis.
NCT04816240 ·Status: UNKNOWN ·Phase: NA
-
Efficacy, Safety and Tolerability of VS-01 in Adult Patients With Acute-on-Chronic Liver Failure and Ascites (UNVEIL-IT)®
NCT05900050 ·Status: TERMINATED ·Phase: PHASE2
-
Human Albumin for the Treatment of Ascites in Patients With Hepatic Cirrhosis
NCT01288794 ·Status: COMPLETED ·Phase: PHASE4
-
Renal and Cardiovascular Effects of Terlipressin in Patients With Cirrhosis and Ascites
NCT00115947 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Incidence & Predictive Factors of Recompensation in Children With Decompensated Cirrhosis as Per the Baveno VII Criteria
NCT06344611 ·Status: NOT_YET_RECRUITING
-
To Study the Effect of Nonselective Beta Blockers in Advanced Stage Liver Disease With Ascites
NCT02649335 ·Status: COMPLETED ·Phase: PHASE3
-
Effects of Long Term Albumin 20% Administration in Patients With Cirrhosis and Ascites.
NCT00968695 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy of Vitamin C on AKI Outcomes in Critically Ill Cirrhotics With Multidrug-resistant Bacterial Infections.
NCT04494451 ·Status: COMPLETED ·Phase: NA
-
Study in Patients With Decompensated Liver Cirrhosis
NCT06380335 ·Status: ACTIVE_NOT_RECRUITING
-
High Dose Albumin in Refractory Ascites
NCT05867602 ·Status: RECRUITING ·Phase: PHASE2
-
Apixaban to Prevent Decompensation of Early Liver Cirrhosis Trial
NCT07726693 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3