National Cancer Institute
Kyiv, 03022, Ukraine
Location status: Recruiting
NCT Number: NCT07295236
The goal of this observational study is to assess the impact of endoscopic vacuum therapy in patients who underwent total gastrectomy due to gastric cancer and developed esophago-jejunal anastomotic leakage. The main outcomes to be investigated are the following:
Primary endpoint: mortality rate Secondary endpoints: morbidity rate, time from AL diagnosis to discharge, patients satisfactory rate.
Interested in participating?
Request Info18 year–90 year
All sexes
Observational
Kyiv, 03022, Ukraine
Location status: Recruiting
Patients who are diagnosed with asophago-jejunal anastomotic leakage will undergo endoscopic vacuum therapy. Local source control may be additionally achieved with para-anastomotic drains.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 90 days after last endo-vac placement
Mortality rate associated with endoscopic vacuum therapy
Time frame: 90 days after last endoscopic vacuum placement
Rate of complications associated with endoscopic vacuum therapy or ineffective local control
Time frame: The number of days from from AL diagnosis to discharge
time from AL diagnosis to discharge
Time frame: 90 days after discharge, 365 days after discharge, 2/3/4/5 years after discharge
Patients satisfactory rate assessed by quality of life questionnaires and patient-reported outcomes scales
Interested in participating?
Request InfoUkrainian Society of Clinical Oncology
Other
Prospective Observational Study on Endo-vac Therapy for Esophago-jejunal Anastomotic Leak
Acronym: ENDO-VAL
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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