Safety and Efficacy of Splenic Artery Embolization to Treat Symptomatic Portal
Trial Snapshot
- Phase
- Not Applicable
- Status
- Withdrawn
- Sponsor
- University of Minnesota
- Locations
- 1
- Primary Endpoint
- Change in Quality of Life
Study Overview
Brief Summary
The primary purpose of this study is to evaluate the safety and efficacy of partial splenic artery embolization in the treatment of symptomatic portal vein hypertension. A secondary aim is to evaluate the relative efficacy of two separate splenic artery embolization techniques, coiling versus particle embolization of the spleen. These two methods will be compared to standard medical management which consist of pain management and fluid draining.
Detailed Description
This is a single center phase I/II study that is designed to assess the safety and efficacy of splenic artery embolization in the setting of symptomatic portal hypertension. All participating investigators have signed the protocol agreement and no investigator will be added until they sign the agreement. The study will not be initiated until FDA and IRB approval is obtained.
The study will consist of a 4 week screening period, day of treatment, and 12-month follow-up period. 60 subjects will be enrolled, with a goal of randomizing 30, at the University of Minnesota Medical Center. Enrollment is expected to take up to 48 months. The collection of data will be accomplished by utilizing a clinical research team that will obtain symptomatic portal hypertension improvement and safety assessments. Efficacy assessments will include; change in portal vein velocity, ascitic fluid production change, reduction in splenic size, and improvement in quality of life (QoL). Safety assessments include subject and investigator reported adverse events, subjective pain, and splenic abscess formation.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 22 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •• Patients who are between 22-70 years of age.
- •Patient must have portal hypertension; as defined by: refractory ascites or unilateral right sided pleural effusions with concomitant liver cirrhosis and splenomegaly (spleen > 11 cm on CT or US).
- •Medically refractive/intolerant, ascites or unilateral right sided pleural effusions consistent with hepatic hydrothorax. Medically refractive defined as those with persistent need for paracentesis or thoracentesis despite maximal doses of diuretics (400 mg spironolactone and 160 mg furosemide per day) or those who are intolerant of furosemide (develop azotemia, electrolyte imbalance, encephalopathy or renal failure) or spironolactone (develop gynecomastia, decreased libido, and hyperkalemia).
- •Patients will need to meet one or more of the following requirements:
- •MELD >18 but <35
- •Anatomic variation making TIPS impossible/difficult
- •Previous failed attempt to place TIPS
- •Unwilling to undergo TIPS
- •History of severe hepatic encephalopathy
- •Thrombosis of the hepatic veins
- •Willing and able to provide informed consent
Exclusion Criteria
- •Patients < 22 and >70 years of age
- •Patients with CLDQ score of >6 or <2
- •Patients with a weight >400 pounds
- •Patients with primary or secondary splenic cancer
- •Currently pregnant
- •Current systemic infection
- •Patients who have undergone prior splenectomy or other splenic surgery
- •Patients who have previously undergone splenic artery embolization for any reason (likely reasons would be trauma or thrombocytopenia)
- •Patients with splenic vascular anatomy that would increase the risk of non-target embolization.
- •Patients who have a INR or platelet count which are not correctable to <1.8 and >35,000 respectively
- •Anaphylaxis to intravenous contrast.
- •Patients diagnosed with Budd-Chiari Syndrome (This will be assessed on pre-intervention CTA)
Arms & Interventions
Control
This arm will undergo no study procedures and continue with best medical management. This entails managing pain and draining excess fluid.
Particle
Randomized to receive either the Embozene or Embosphere particles
Intervention: Particle (Device)
Coil
Randomized to receive either Ruby or Interlock detachable coils
Intervention: Coil (Device)
Outcomes
Primary Outcomes
Change in Quality of Life
Time Frame: pre-procedural (baseline) and at 1, 3, 6, and 12 month follow-up visits
Administration of the Chronic Liver Disease Questionnaire (CLDQ)
Incidence of Treatment Adverse Events
Time Frame: Patients will be evaluated for adverse events post procedural at 72hrs, 1 week, and 1, 3, 6, and 12 months
Evaluation of all procedure-related adverse events (PRAE) and serious adverse events (SAE)
Secondary Outcomes
- Ascites Production(pre-procedural and at 1, 3, and 6 months)
- Portal Vein Velocity(pre-procedural and at 1, 6 and 12 months)
- Splenic Size(pre-procedural and at 1,3,6 and 12 months)