Skip to content

Refluxassociated changes of the remant esophagus after esophagectomy and gastric interposition– Gastrointestinal Function Testing during long time follow up in patients with esophageal cancer

Refluxassociated changes of the remant esophagus after esophagectomy and gastric interposition– Gastrointestinal Function Testing during long time follow up in patients with esophageal cancer

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011123
Enrollment
75
Registered
2016-09-30
Start date
2016-10-04
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

K21.0

Interventions

Group 1: Gastrointestinal Function Testing Using laryngopharyngeal PH Probe (Restech) and conventional esophageal pH monitoring (impedance).

Sponsors

Klinik und Poliklinik für Allgemein-, Viszeral- und TumorchirurgieUniklinik Köln
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients with esophagus carcinoma that underwent hybrid Ivor Lewis esophagectomy and that gave their written consent

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Patients will undergo 24-h laryngopharyngeal pH measurement (Restech)and intraluminal impedance pH-monitoring at the same time so that the relationship between the two techniques can be evaluated (for assessment of gastrointestinal function).

Secondary

MeasureTime frame
Also they will undergo a routine check-up program with a surveillance endoscopie. To evaluate the symptoms patients are asked to fill out a standardized questionnaire (GERD HRQL). When we collected all the data we can evaluate the relationship between the two different techniques and the symptoms of the patient.

Countries

Germany

Contacts

Public ContactHans Fuchs

Klinik und Poliklinik für Allgemein-, Viszeral- und TumorchirurgieUniklinik Köln

hans.fuchs@uk-koeln.de+49-221-478-4801

Outcome results

None listed

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