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

Application observation to evaluate quality of life, recurrences and surgical-related or postoperative complications after laparoscopic hiatus reconstruction using the product DynaMesh®-DELTA - AWB-DEL

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033093

Enrollment

321

Registered

2023-11-29

Start date

2023-04-01

Completion date

Unknown

Last updated

2026-08-03

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 dorsal hiatoplasty with additional mesh implantation (DynaMesh®-DELTA).

Eligibility

Sex/Gender

All

Age

18 Years to 86 Years

Inclusion criteria

Inclusion criteria: - of legal age and legally competent - Symptomatic hiatal hernia with indication for surgical treatment using a DynaMesh®-DELTA mesh implant

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
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). Assessment of safety through the frequency and severity of peri- and postoperative complications, frequency of mesh-related complications	—

Secondary

Measure	Time frame
Patient satisfaction	—

Countries

Germany

Contacts

Public ContactFlorian Thomas

Vivantes Klinikum Am Urban

Florian.Thomas@vivantes.de+49 30-130225401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026