A single center prospective observational non-randomized clinical study to assess the safety and efficacy of placement of a new esophageal self-expandable metal stent (SEMS) for palliation of patients with malignant dysphagia.
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Complication: incidence of perforation
Timeframe: 6 months
Complication: incidence of hemorrhage
Timeframe: 6 months
Complication: incidence of fistula formation
Timeframe: 6 months
Complication: incidence of gastroesophageal reflux
Timeframe: 6 months
Complication: incidence of stent migration
Timeframe: 6 months
Efficacy: clinical outcome
Timeframe: 6 months
Efficacy: incidence of patients receiving technical successful stent placement
Timeframe: 1 day, during stent placement