Condition: Cirrhosis · Esophageal and Gastric Varices · Ascites · Sponsor: Asian Institute Of Medical Sciences
The APIXABAN-PK trial is a prospective, randomized, single-blind, placebo-controlled study designed to evaluate the efficacy and safety of apixaban in combination with carvedilol versus placebo with carvedilol in preventing portal hypertension-related complications in patients with cirrhosis. Conducted at the Gastroenterology and Hepatology Department and Clinical Trials Unit (CTU) of Asian Institute of Medical Sciences (AIMS) Hospital, Hyderabad, Pakistan, the trial will enroll eligible cirrhotic patients with portal hypertension. Participants will be followed for 12 months to monitor hepatic decompensation events, variceal bleeding, portal vein thrombosis, and mortality, while safety and tolerability of apixaban will be closely assessed. This study aims to provide local evidence for apixaban use in cirrhosis management in Pakistan.
This description comes directly from the study's public registry record.
Fatima Nadeem Dr, Pharm-D, Mphil · +923080744996 · fatima.nadeem2401@gmail.com
Always discuss trial participation with your own doctor first.
| Asian Institute of Medical Sciences | Hyderābād, Sindh, Pakistan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07521332