Application observation to evaluate quality of life, recurrences and surgical-related or postoperative complications after laparoscopic hiatus reconstruction using the product DynaMesh®-DELTA
- Conditions
- K44Diaphragmatic hernia
- Registration Number
- DRKS00033093
- Lead Sponsor
- FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 133
Inclusion Criteria
of legal age and legally competent
- Symptomatic hiatal hernia with indication for surgical treatment using a DynaMesh®-DELTA mesh implant
Exclusion Criteria
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 Assessment of the performance of the surgical technique and the mesh implant (DynaMesh®-DELTA) in relation to the frequency of recurrent hernias (only symptomatic recurrences).<br>Assessment of safety through the frequency and severity of peri- and postoperative complications, frequency of mesh-related complications
- Secondary Outcome Measures
Name Time Method Patient satisfaction