Last updated: March 11, 2019
Sponsor: New York Presbyterian Hospital
Overall Status: Active - Recruiting
Phase
N/A
Condition
Hyponatremia
Scar Tissue
Hepatic Fibrosis
Treatment
N/AClinical Study ID
NCT03414398
1710018603
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
primary liver cirrhosis
receiving care at the study cite
no evidence of hepatic encephalopathy if the subject is providing consent
Exclusion
Exclusion Criteria:
no documentation of cirrhosis
unable to confirm diagnosis of cirrhosis by imaging or pathology
Study Design
Total Participants: 273
Study Start date:
December 26, 2017
Estimated Completion Date:
July 01, 2021
Study Description
Connect with a study center
New York Presbyterian Hospital - Weill Cornell Medicine
New York, New York 10021
United StatesActive - Recruiting

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