Clinical Trials Directory

Trials / Completed

CompletedNCT03759158

N-Acetyl Cysteine in the Prevention of Contrast Induced Nephropathy in Cirrhosis of Liver-NEPHRO Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Institute of Liver and Biliary Sciences, India · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Contrast induced nephropathy has an incidence of 7-11 % in patients undergoing Contrast imaging for various conditions. The risk associated with the development of CIN are still under evaluation. Even with patients having normal kidney functions there is a risk of contrast induced nephropathy hence the need for markers which could predict injury. Cirrhosis of liver predisposes patient to Kidney abnormalities as these patients lower renal reserve and can have various conditions like Hepatorenal syndrome, Sepsis, ATN. Contrast imaging is vital for ruling out conditions like Hepatocellular Carcinoma in patients of cirrhosis of liver. Presently there is no study in cirrhosis of liver which studies the Effect of N-acetyl cysteine before and after contrast imaging in the prevention Of CIN. The incidence of CNI is cirrhosis is also an avenue which requires more studies and also there is a need for formulation of a Score to predict this CIN. Hence this study is being done to assess the incidence of CNI and the role of N-Acetyl cysteine in Preventing CNI.

Conditions

Interventions

TypeNameDescription
DRUGN-Acetyl CysteineNAC 1200 mg twice daily one day prior to the procedure and on the day of the procedure.
DRUGPlacebo Oral TabletPlacebo Oral Tablet twice daily.

Timeline

Start date
2018-12-01
Primary completion
2019-01-15
Completion
2019-01-15
First posted
2018-11-29
Last updated
2019-11-04

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT03759158. Inclusion in this directory is not an endorsement.