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Eso-Sponge Registry

NCT02662777 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 108

Last updated 2024-08-14

No results posted yet for this study

Summary

This international, prospective and multicenter registry was designed to collect clinical evidence for the endoscopic vacuum treatment using Eso-SPONGE® for anastomotic leakage after esophageal resection or iatrogenic or spontaneous esophageal perforation.

Conditions

  • Leakage After Esophagectomy
  • Leakage After Gastrectomy
  • Perforation of the Esophagus

Interventions

DEVICE

Eso-SPONGE® vacuum treatment

Sponsors & Collaborators

  • Universitätsklinikum Kiel

    collaborator UNKNOWN

  • Aesculap AG

    lead INDUSTRY

Principal Investigators

  • Clemens Schafmayer, Prof. Dr. · Universitätsklinikum Kiel

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02662777 on ClinicalTrials.gov