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

Esophageal Cancer Clinical Trial

— ESPY  

Official title:

Prospective, Multi-centre, Exploratory and Observational One-arm Study to Evaluate Preemptive Endoluminal Vacuum Therapy to Prevent Anastomotic Leakage After Esophagectomy Due to Esophageal Cancer

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06097078
• Other study ID #: AAG-O-H-2209
• Status: Not yet recruiting
• Start date: June 2024
• Est. completion date: October 2025

Study information

• Verified date: April 2024
• Source: Aesculap AG
• Contact: Jaume Garcia López, Dr.
• Phone: +34935866200
• Email: info[@]bbraun.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Description:

Prospective, multi-centre, exploratory and observational one-arm study to evaluate preemptive endoluminal vacuum therapy to prevent anastomotic leakage after esophagectomy due to esophageal cancer.

The study comprises a maximum of 5 visits per protocol. At visit 0, informed consent will be obtained, and the patient will be checked for compliance with all inclusion criteria and no exclusion criteria in the study. Demographic characteristics, medical history and oncological parameters will be collected. At visit 1 ttMILE will be carry out and immediately (0-24h) after completion of the anastomosis, in patients who meet selection criteria, the Eso-SPONGE® will be placed endoscopically via an overtube, as usual clinical practice of the centre. The tube will be routed transnasally and then connected to a vacuum pump, generating a continuous negative pressure of 75 mmHg. The Eso-SPONGE system will be checked 6-hourly for leakage and dislocation. The sponge will be removed after 4-6 days (V2). After removal, the anastomosis and the gastric tube will be assessed endoscopically to exclude leakage and evaluate ischemia and stenosis, and the pylorus will be evaluated for spasm. The next visits (V3 and V4) will be carried out at 30 and 90 days after the intervention has been placed. Leakage, ischemia and stenosis will be clinically evaluated at each visit and a new endoscopy will be performed in patient who show symptoms.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 44
• Est. completion date: October 2025
• Est. primary completion date: June 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Anastomotic Leak
• Esophageal Cancer
• Esophageal Neoplasms
• Esophagus Cancer

Intervention

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

Locations

Country	Name	City	State
Spain	Hospital Clinic de Barcelona	Barcelona	Catalunya

Sponsors (2)

Lead Sponsor	Collaborator
Aesculap AG	B.Braun Surgical SA

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of patients with anastomotic leakage	Anastomotic leakage (AL) is a severe complication following gastric and esophageal surgery. Anastomotic leakage occurs in 5-30% of patients after esophagectomy and may be further complicated by mediastinitis, sepsis, multiple organ failure, or death. The primary objective of the study is to evaluate the potential protective effect of prophylactic preemptive endoluminal vacuum therapy on esophageal-gastric anastomosis dehiscence after esophagectomy.	throughout the duration of the study (until last follow-up at postoperative day 90)
Secondary	Comprehensive Complication Index	The Comprehensive Complication Index (CCI®) calculates the overall morbidity of a patient after any surgical intervention based on the complication grading by the "Clavien-Dindo Classification" (CDC). The Comprehensive Complication Index (CCI®) reflects the gravity of this overall complication burden on the patient on a scale from 0 (no complication) to 100 (death).	Postoperative day 30 and day 90
Secondary	Description of Adverse Events	All the Adverse Events reported during the study will be described together with their characteristics, noting those related with the investigational device application.	throughout the duration of the study (until last follow-up at postoperative day 90)
Secondary	Rate of postoperative ischemia	The different grades of postoperative ischemia at Visit 1, Visit 2 and Visit 3	Postoperative day 30 and day 90
Secondary	Rate of postoperative mortality	The percentage of patients who died along the study will be described in terms of absolute and relative frequencies, as well as causes for death and time until death regarding investigational device application.	Postoperative day 30 and day 90
Secondary	Rate of postoperative stenosis	The percentage of postoperative stenosis at Visit 1, Visit 2 and Visit 3, as well as along the study	throughout the duration of the study (until last follow-up at postoperative day 90)
Secondary	Length of hospitalization	time elapsed until reaching the "fit for discharge criteria" regarding investigational device application	until discharge (approximately 10 days postoperatively)
Secondary	Re-admissions to hospital	The percentage of patients re-admitted along the study will be described; as well as the time elapsed until re-admission regarding investigational device application	throughout the duration of the study (until last follow-up at postoperative day 90)
Secondary	Surgical reoperations	The percentage of patients with surgical reoperations along the study will be described; as well as the time elapsed until surgical reoperation regarding investigational device application	throughout the duration of the study (until last follow-up at postoperative day 90)
Secondary	Anastomotic leakage free survival	Event free survival at 30 days and at 90 days will be analyzed using Kaplan-Meier method, considering the anastomotic leakage reported during the study. Patients with no anastomotic leakage during the analyzed period will be censored at last follow-up date	throughout the duration of the study (until last follow-up at postoperative day 90)
Secondary	Rate of intraluminal hemorrhage	The percentage of patients with intraluminal hemorrhage along the study will be described in terms of absolute and relative frequencies; as well as the time elapsed until hemorrhage regarding investigational device application. Additionally, to see the distribution of the time until intraluminal hemorrhage Kaplan-Meier method will be performed at 90 days (patients with no intraluminal hemorrhage during the study will be censored at last follow-up date).	throughout the duration of the study (until last follow-up at postoperative day 90)