Cross-section Band Ligation Versus Stepladder Band Ligation of Esophageal Varices
Launched by TANTA UNIVERSITY · Mar 11, 2025
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at two different techniques for treating esophageal varices, which are enlarged veins in the esophagus that can occur in patients with liver disease. The study aims to compare the "cross-section band ligation" technique with the "stepladder band ligation" technique to see which one is more effective in preventing complications, such as bleeding, and to check for any side effects. Participants will undergo a series of exams and procedures, including endoscopies, to assess their condition and receive treatment every two to four weeks until the varices are gone. After treatment, they will have follow-up visits to monitor for any recurrence of varices and evaluate their overall health.
To be eligible for this trial, participants should be over 18 years old, have liver cirrhosis, and show signs of medium to large esophageal varices. Certain individuals, such as those with a history of bleeding from varices, those on specific medications, or those with severe heart or lung conditions, cannot participate. Throughout the trial, participants can expect regular check-ups to monitor their health, as well as support and guidance from the research team. This trial is currently recruiting participants, and it provides an opportunity to contribute to important research that could improve treatment for patients with esophageal varices.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Aged \>18 years.
- • Cirrhotic patients.
- • Endoscopic evidence of medium/large-sized esophageal varices.
- Exclusion Criteria:
- • History of variceal bleeding or previous primary prevention of varices.
- • Portal vein thrombosis or previous porto-systemic shunts as TIPS.
- • Patients on drugs affecting portal pressure (beta blockers, nitrates).
- • Advanced cardiovascular disease including acute myocardial infarction, atrio-ventricular block, congestive heart failure, chronic peripheral ischemia, and severe bradycardia.
- • Patients with severe respiratory diseases (COPD, bronchial asthma).
- • Uncontrolled diabetes mellitus.
- • Renal impairment.
- • Hepatocellular carcinoma.
- • Allergy to carvedilol.
- • Pregnancy or lactation.
About Tanta University
Tanta University is a prestigious academic institution located in Egypt, dedicated to advancing medical research and education. As a clinical trial sponsor, Tanta University leverages its extensive resources and expertise to conduct innovative research initiatives aimed at improving health outcomes. The university collaborates with a network of healthcare professionals, researchers, and institutions to facilitate rigorous clinical trials across various medical disciplines. Committed to ethical standards and scientific integrity, Tanta University strives to contribute to the global body of knowledge while fostering the next generation of medical professionals.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Tanta, Gharbyea, Egypt
Patients applied
Trial Officials
Nabila A Elgazzar, MD
Principal Investigator
Tropical medicine and infectious diseases Department, Faculty of Medicine, Tanta University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported