Evaluation of preoperative endoscopic pyloric dilation for prevention of postoperative pyloric stenosis after Ivor-Lewis-esophagectomy

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00028044

Enrollment

Registered

2022-02-04

Start date

2020-10-21

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

C15 K31

Interventions

Group 1: endoscopic pneumatic pyloric dilation. Group 2: historic comparative group

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: age >18 years, written consent, intended Ivor-Lewis-esophagectomy due to esophageal carcinoma, benign tumours oder functional disease.

Exclusion criteria

Exclusion criteria: age < 18 years, pregnancy, no written consent, patients with pyloroplastic or G-POEM of the pylorus, esophageal stenosis.

Design outcomes

Primary

Measure	Time frame
Need for postoperative endoscopic pyloric dilation and number of repetions in the first 2 months.	—

Secondary

Measure	Time frame
Technical success, complication rate for bleeding, Perforation and pneumonia, rate of anastomotic leakage, anastomotic stenosis, need for surgical pyloroplastic, need for inpatient treatment.	—

Countries

Germany

Contacts

Public ContactMartin Hemmerich

Elisabeth-Krankenhaus Essen, Abteilung für Chirurgie

m.hemmerich@contilia.de0201-897-3301

Outcome results

None listed

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