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EUS-guided Combined Therapy Versus Beta Blocker Therapy in Primary Prophylaxis o GOV II and IGV I

Not Applicable
Conditions
Gastric Varix
Cirrhosis
GastroIntestinal Bleeding
Interventions
Procedure: Coils + Cyanoacrylate Group + beta-blocker
Drug: beta blocker therapy
Registration Number
NCT04075760
Lead Sponsor
Instituto Ecuatoriano de Enfermedades Digestivas
Brief Summary

The EUS-guided combined therapy of coilingand 2-octyl-cyanoacrylate in patients with gastric varices reduced rebleeding and need for reintervention in comparison to EUS-guided coiling alone.The purpose of this study is to determine the efficacy of the primary prophylaxis of GOV II and IGV I with the EUS combined therapy versus beta blocker therapy in patients GOV II and IGV that have never bleed.

Detailed Description

Gastric variceal bleeding is a severe condition associated with a high mortality. Bleeding from varices bleeding will be defined as the occurrence of hematemesis and/or melena requiring \>2 U of blood or a decrease of 2 gm/dl of hemoglobin if no blood transfusion is given, with the confirmed endocopic visualization of GOV II and IGV I.

The beta blocker therapy is an effective method for the prevention of the first esophageal variceal bleeding; however, the efficacy in preventing first gastric variceal bleeding is controversial.

The investigators aimed to compare the efficacy in preventing the first gastric variceal bleeding in patients with documented GOV II and IGV I.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
26
Inclusion Criteria
  • Above 18 years old
  • Writeen informed consent provided.
  • Proven GV (GOV II or IGV I) on esophagogastroduodenoscopy and EUS.
  • Gastric varices with high-risk of bleeding (large diameter, high MELD score, presence of portal hypertensive gastropathy)
  • Patient preference for EUS-guided therapy.
Exclusion Criteria
  • Under 18 years old.
  • Refuse to sign written informed consent.
  • Pregnancy or nursing.
  • Previous treatment of gastric varices.
  • Non-cirrhotic portal hypertension
  • Concurrent hepato-renal syndrome and/or multi-organ failure.
  • Proven malignancy including hepatocellular carcinoma
  • Platelet count less than 50,000/ml or International Normalized Rate (INR) >2.
  • Severe ascites that increases the distance between gastric or duodenal and gallbladder walls.
  • Esophageal stricture.
  • Uncontrolled coagulopathy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
EUS-guided combined therapyCoils + Cyanoacrylate Group + beta-blockerPatients with endoscopic and EUS documented GOV II and IGV I will be included. Procedure will be performed under general anesthesia using a linear array therapeuthic echoendoscope, coils and cyanoacrylate will be injected within the feeder vessel under EUS and fluroscopic guidance.
Beta Blocker (Propranolol)beta blocker therapyo Beta-blocker (propranolol) will be started at dose of 20 mg twice daily. The principle of incremental dosing was used to achieve the target heart rate for propranolol. The dose will be increased every alternate day to achieve a target heart rate of 55/min or to the maximal dose to 360 mg/day if the medication was well tolerated and the systolic blood pressure was \> 90 mm Hg. On the occurrence of intolerable adverse effects, systolic blood pressure \< 90 mm Hg or pulse rate \< 55/min, the dose of the medication was decreased step-wise, and eventually stopped if these adverse events persisted. Reintroduction of the medication will be attempted if cessation of the medication did not result in improvement of the reported side-effect.
Primary Outcome Measures
NameTimeMethod
Bleeding rate secondary to gastric varices12 months

Number of patients with melena or hematemesis accompanied by Hemoglobin drop \> 2g/dL

Mortality secondary to gastrointestinal bleeding12 months

mortality rate

Secondary Outcome Measures
NameTimeMethod
Number of reinterventions12 months

number of endoscopic or endoscopic ultrasound procedures requiered for the management of gastri varices

Trial Locations

Locations (1)

Instituto Ecuatoriano de Enfermedades Digestivas

🇪🇨

Guayaquil, Guayas, Ecuador

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