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Clinical Trial Summary

Patients who underwent anti-reflux surgery were divided into two groups. In the I group Nissen fundoplication was supplemented with suturing wrap to the crura or the body of stomach using two non-absorbable stitches on each side. Control group included patients who underwent classic Nissen fundoplication without wrap fixation. All patients were assessed before and after surgery using validated symptoms and quality of life (GERD-HRQL) questionnaires, 24-h impedance-pH monitoring and barium-swallow.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04335734
Study type Interventional
Source Odessa National Medical University
Contact
Status Completed
Phase N/A
Start date November 1, 2012
Completion date May 28, 2019

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