Patients who underwent laparoscopic repair of large hiatal hernias and anterior
fundoplication with mesh are examined for their recurrence rate one year after surgery.
Procedure: repair of giant hiatal hernia with mesh and anterior fundoplication
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Full eligibility criteria for NCT03025932
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Age older than 18 years
Initially suffering from large hiatal hernia (>20% of the stomach in the thoracic cavity)
Performance of laparoscopic hiatal hernia repair with mesh and anterior fundoplication
Informed Consent as documented by signature (Appendix: Informed Consent Form)
Performance of any other anti-reflux surgery such as Toupet- or Nissen-fundoplication
Performance of anterior fundoplication without mesh
Women who meet the inclusion criteria but are pregnant or breast feeding or have the intention to become pregnant during the course of the study
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Tris trial is registered with FDA with number: NCT03025932. The sponsor of the trial is PD Dr. Urs Zingg and it is looking for 50 volunteers for the current phase.
Official trial title: Clinical vs. Radiological Recurrence Rate After Laparoscopic Repair of Large Hiatal Hernia With Mesh and Anterior Fundoplication
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