A prospective randomized clinical trial to evaluate efficacy and safety of combined EUS-HGS and ERCP compared to ERCP for bilateral biliary decompression in advanced malignant hilar biliary obstruction. The primary outcome will be technical success, clinical success, procedural duration, and re-interventions. Secondary outcomes will be the rate of adverse events. patients will be followed up at 1 and 3 month intervals
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Technical success
Timeframe: during the procedure
Procedural duration
Timeframe: at the end of the procedure
Clinical success
Timeframe: 3 month
Re-interventions
Timeframe: 3 month