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Clinical Trials in Spain / NCT06097078
Active, not recruiting Observational

Endoluminal Vacuum Therapy to Prevent Anastomotic Leakage After Esophagectomy Due to Esophageal Cancer

NCT06097078 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2024-10-07
Last updated
2026-09-21

Condition(s) studied

Esophageal CancerEsophagus CancerAnastomotic Leak

Investigational drug(s) / intervention(s)

Eso-SPONGE®

Eso-SPONGE®: minimally invasive treatment and prevention of anastomotic leakages and perforations in the upper gastrointestinal tract (upper GIT)

Study summary

A prospective, multi-centre, exploratory and observational one-arm study to evaluate preventive Endoluminal Vacuum Therapy(pEVT) to prevent anastomotic leakage after esophagectomy due to esophageal cancer. The main objective is to evaluate the potential protective effect of prophylactic preemptive endoluminal vacuum therapy on esophageal-gastric anastomosis dehiscence after esophagectomy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Scheduled for total minimally invasive (laparoscopic or robotic and thoracoscopic) transthoracic Ivor Lewis esophagectomy (ttMILE) due to esophageal cancer and subsequent eso-SPONGE application to prevent anastomotic leakage * Patients able to read and understand the Patient Information Sheet and sign, if accepted, the Informed Consent Form * Patients able, at the discretion of the investigator, to comply with the requirements of the study and without impediments to follow the instructions and assessments throughout the study. Exclusion Criteria: * Patients undergoing transhiatal esophagectomy without reconstruction, open Ivor Lewis esophagectomy or other esophageal resections different to ttMILE. * Multi-organ resection during the esophagectomy. * Emergent-urgent esophagectomy. * Coloplasty or small bowel plasty. * Necrotic tissue/gangrene. * Blood clotting disorder. * Bleeding esophageal varices. * Sponge placement required directly on major vessels. * Patients with known sensitivities or allergies to its components * Participation in any other clinical trial and use of any drug or experimental device, currently or in the 4 weeks prior to inclusion in the study. * Women who are pregnant, suspected of being pregnant or breastfeeding.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hospital Clinic de Barcelona Barcelona Catalonia

More Aesculap AG trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06097078 on ClinicalTrials.gov ↗ ← All trials in Spain