Retrospective application observation to evaluate quality of life, recurrences and surgical-related or postoperative complications after laparoscopic hiatus reconstruction using the DynaMesh®-HIATUS product
- Conditions
- K44Diaphragmatic hernia
- Registration Number
- DRKS00034087
- Lead Sponsor
- FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
All patients who underwent surgical treatment of hiatal hernia using a DynaMesh®-HIATUS mesh implant at Marien Hospital Düsseldorf between January 1, 2016 and October 31, 2021 were included.
Beyond this, there are no study-related inclusion criteria.
Exclusion Criteria
Since this is an observational study as part of usual treatment practice, there are no study-related exclusion criteria.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method