|
|
|
|
|
|
Sponsors and Collaborators: |
Taipei Veterans General Hospital,Taiwan National Science Council, Taiwan |
Information provided by: | Taipei Veterans General Hospital,Taiwan |
ClinicalTrials.gov Identifier: | NCT00567216 |
Gastric variceal bleeding has a very high rebleeding rate even after endoscopic variceal injection of cyanoacrylate (GVO) which is considered the first choice of endoscopic treatment. Beta-blocker (BB) is effective to lower portal pressure. We hypothesized combination of GVO and BB can further decrease the rebleeding rate.
Condition | Intervention | Phase |
Liver Cirrhosis and Hepatoma. Gastric Variceal Bleeding |
Drug: Nadolol |
Phase IV |
MedlinePlus related topics: | Cirrhosis Endoscopy |
ChemIDplus related topics: | Nadolol BaseLine |
Study Type: | Interventional |
Study Design: | Prevention, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study |
Official Title: | A Randomized Tril of Endoscopic Cyanoacrylate Obliteration vs. Nadolol |
Estimated Enrollment: | 120 |
Study Start Date: | April 2007 |
Estimated Study Completion Date: | July 2010 |
Arms | Assigned Interventions |
G: No Intervention
Endoscopic injection of cyanoacrylate alone
|
|
C: Active Comparator
Combination of GVO and nadolol
|
Drug: Nadolol
Starting from 20 mg daily, titrated weekly to decrease heart rate more than 25 % of baseline, administrated during the whole study period
|
Gastric varies (GV) rarely rupture. However should it occur, the outcome would be worse than rupture of esophageal varies (EV). Rupture of GV is characteristic of a higher rebleeding rate, a requirement for a larger amount of blood transfusion and a higher mortality. Up to date, the treatment of GV bleeding (GVB) is still sub-optimal in contrast to the treatment of EV bleeding. The management of GV has been focused on treatment of acute GVB. Various specific methods are used to control GVB and prevent rebleeding; however they were far from ideal. It is because GV are usually larger vessels formed in deeper submucosa and connect to the spontaneous gastrorenal shunt which creates a fast blood flow. Therefore, voluminous blood in the larger diameter GV leads to exsanguine bleeding when ruptured. A variety of endoscopic methods, which include injection of sclerosants, tissue adhesive (cyanoacrylate), thrombin and ligation with rubber bands, detachable nylon loop and steel snares, are applied to control acute GV bleeding with variable successful rates (50~100%) and rebleeding rates (20~90%). The successful rate of endoscopic cyanoacrylate injection to arrest active GVB is more consistent around 90~100% and rebleeding rate is around 30~40%. The recent International Consensus Meeting endorsed that endoscopic cyanoacrylate injection is the first line treatment for acute GVB. The embolic complications, either septic & aseptic, are not uncommon. Expertise is also required to reduce the embolic complications and instrumental injuries. Therefore, the efficacy of specific treatment for GVB is sub-optimal, consecutive innovation of new methods are required to improve the prognosis of GVB. Non-selective beta-blocker is effective to reduce rebleeding from esophageal varices. However, its effect on gastric variceal hemorrhage has never been proven.
This is an important issues prompted by current portal hypertension experts. We have much experience in the treatment of gastric variceal bleeding and published fruitful results in high ranking journal. Therefore, we design a randomized trial to compare the effect of endoscopic cyanoacrylate injection obliteration versus non-selective beta-blocker in the secondary prevention of acute gastric variceal bleeding.
Ages Eligible for Study: | 18 Years to 80 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Ming-Chih Hou, MD | 886-2-28712111 ext 3763 | mchou@vghtpe.gov.tw |
Contact: Han-Chieh Lin, MD | 886-2-28712111 ext 3349 | hclin@vghtpe.gov.tw |
China, Taiwan | |||||
Veteran General Hospital-Taipei | Recruiting | ||||
Taipei city, Taiwan, China, 11217 | |||||
Contact: Ming-Chih Hou, MD 886-2-28712111 ext 3763 mchou@vghtpe.gov.tw | |||||
Principal Investigator: Ming-Chih Hou, MD |
Taipei Veterans General Hospital,Taiwan |
National Science Council, Taiwan |
Principal Investigator: | Ming-Chih Hou, MD | Taipei Veterans General Hospital,Taiwan |
Study ID Numbers: | nsc96-2314-B-075-037-MY3, IRB-96-04-01 |
First Received: | December 2, 2007 |
Last Updated: | December 2, 2007 |
ClinicalTrials.gov Identifier: | NCT00567216 |
Health Authority: | Taiwan: Department of Health |
|
|
|
|