Safety and Efficacy of Conventional Compared to Segmented Esophageal Fully Covered Self-expanding Metal Stents: a Retrospective Multicenter Case-Control Study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00034173

Enrollment

160

Registered

2024-05-17

Start date

2023-11-15

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

K22.2 C15.9

Interventions

Group 1: Patients that received conventional-esophageal fully covered self-expanding metal stents for the treatment of esophageal strictures Group 2: Patients that received segmented 2esophageal fully

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Benign esophageal stenosis Malign esophageal stenosis

Exclusion criteria

Exclusion criteria: Esophageal stenting for other reasons than stenosis

Design outcomes

Primary

Measure	Time frame
Clinical Success (migration and stent occlusion)	—

Secondary

Measure	Time frame
severe clinical complications	—

Countries

Germany

Contacts

Public ContactThomas von Hahn

Asklepios Krankenhaus Barmbek

T.hahn@asklepios.com+491818820

Outcome results

None listed

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