VAC-Stent registry: Data collection on the treatment of gastrointestinal leakage by the use of combination of covered nitinol stent and negative pressure wound treatment

VAC-Stent registry: Data collection on the treatment of gastrointestinal leakage by the use of combination of covered nitinol stent and negative pressure wound treatment - VAC-Stent registry

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00020782

Enrollment

500

Registered

2020-06-05

Start date

2020-07-01

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

K22.3 K63.1

Interventions

Group 1: Patients with leakage in the oesophagus or colon who are treated with the VAC stent. This study is a registry without any reference products. The treatment with the stent and any complication

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Presence of a written consent of the patient • Patients treated with the VAC stent

Exclusion criteria

Exclusion criteria: • Accommodation in an institution under court or administrative order

Design outcomes

Primary

Measure	Time frame
Development of a registry and data acquisition for quality assurance and application of the VAC stent	—

Countries

Germany

Contacts

Public ContactMarkus M. Heiss

Klinik für Viszeral-, Tumor-, Transplantations- und Gefäßchirurgie, Klinikum Köln-Merheim

HeissM@kliniken-koeln.de0221/8907-3770

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026