Usefulness of abdominal binders as postoperative treatment following incisional hernia repair in sublay technique

Usefulness of abdominal binders as postoperative treatment following incisional hernia repair in sublay technique - ABIHR II pilot study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00017410

Enrollment

Registered

2019-09-04

Start date

2020-01-27

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

K43.2 K43.99

Interventions

Group 1: No carrying of an Abdominal binder following incisional hernia repair in Sublay technique Group 2: Carrying of an Abdominal binder for 2 weeks during daytime following incisional hernia repai

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age > 18 years Patients who underwent incisional hernia repair in sublay technique Subscribed consent form

Exclusion criteria

Exclusion criteria: Pregnancy No hernia gap closure intraoperative (as screening failure) Physical and psychological condition which not allows to understand and/or subscribe consent form

Design outcomes

Primary

Measure	Time frame
Pain on the 14. postoperative day using VAS-Score	—

Secondary

Measure	Time frame
Quality of life one year after surgery Relapse rate one year after surgery Rate of seroma formation 2 weeks after surgery	—

Countries

Germany

Contacts

Public ContactPedro Ortiz Rojas

Helios Klinikum Berlin-Buch

pedro.ortiz-rojas@helios-gesundheit.de.030/940112794

Outcome results

None listed

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