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Retrospective application observation to evaluate quality of life, recurrences and surgical-related or postoperative complications after laparoscopic hiatus reconstruction using the DynaMesh®-HIATUS product

Retrospective application observation to evaluate quality of life, recurrences and surgical-related or postoperative complications after laparoscopic hiatus reconstruction using the DynaMesh®-HIATUS product - Retro-AWB-HIA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00034087
Enrollment
72
Registered
2024-04-29
Start date
2022-04-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

K44

Interventions

Group 1: All patients suffered from a symptomatic hiatal hernia and underwent surgical treatment of the hiatal hernia using a DynaMesh®-HIATUS mesh implant
their age at the time of the operation was between 18 and 85 years.

Sponsors

FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

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

Exclusion criteria: Since this is an observational study as part of usual treatment practice, there are no study-related exclusion criteria.

Design outcomes

Primary

MeasureTime frame
This observational study is primarily intended to assess the performance of the product. Performance parameters are: Recurrent herniation

Secondary

MeasureTime frame
Perioperative complications and follow-up data to assess safety

Countries

Germany

Contacts

Public ContactKonstantinos Zarras

Marienhospital Düsseldorf

chirurgie@marien-hospital.de+49 (02 11) 44 00-20 0

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026