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Study identifier: NCT07310316 Synced from ClinicalTrials.gov · July 29, 2026
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Efficacy and Safety of Variceal Embolization Combined With Partial Splenic Artery Embolization for Variceal Bleeding in Cavernous Transformation of Portal Vein.

Condition: Cavernous Transformation of Portal Vein · Gastroesophageal Varices Bleeding  ·  Sponsor: Air Force Military Medical University, China

PhaseNA
Planned participants26
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The management of variceal bleeding in patients with cavernous transformation of portal vein (CTPV) generally adheres to the principles applied to cirrhotic portal hypertension, including pharmacological therapy, endoscopic intervention, transjugular intrahepatic portosystemic shunt (TIPS), and surgery. However, the distinct hemodynamic profile caused by portal vein occlusion in CTPV introduces specific therapeutic challenges: 1. Conventional pharmacological and endoscopic treatments often yield suboptimal outcomes. 2. Splenectomy with periesophagogastric devascularization is associated with significant complication rates and elevated perioperative mortality. 3. The feasibility of TIPS depends on sufficient portal venous inflow to ensure stent patency, while also carrying a risk of hepatic encephalopathy. Based on these considerations, the investigators hypothesize that for patients with extensive portal thrombosis and inadequate portal inflow who are ineligible for TIPS, a combination of variceal embolization and partial splenic artery embolization may reduce portal pressure and decrease the risk of esophagogastric variceal bleeding. To evaluate this hypothesis, a retrospective cohort study has been designed.

This description comes directly from the study's public registry record.

Talk to the study team

Jun Tie, M.D.,Ph.D.  ·  +862984771537  ·  tiejun7776@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Air Force Military Medical UniversityXi'an, Shaanxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07310316