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Usage of Biological Patch Versus Plastic in the Laparoscopic Repair of Hiatal Hernias

Hiatal Hernia Clinical Trial

Official title:
Randomized Control Trial (RCT) That the Usage With Biological Patch Versus Plastic in the Laparoscopic Repair

Clinical Trial Summary

The purpose of this study is to observe the effective and safety in the laparoscopic repair of hiatal hernia using biological patch versus plastic.

Clinical Trial Description

observation indicator:

1. incidence rate of complications,

2. postoperative hospital stay

3. readmission rate in 1st month after operation

4. recurrence rate after operation

5. hospitalization costs

6. Self-evaluation of gastroesophageal reflux symptoms and quality of life(QOL) in 6th-month, 1st-year,2nd-year,3rd-year,4th-year and 5th-year after operation ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02328248
Study type Interventional
Source Xijing Hospital of Digestive Diseases
Contact
Status Active, not recruiting
Phase Phase 2/Phase 3
Start date July 2014
Completion date December 2016
View Details
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