Actively Recruiting
Gastric Preconditioning by Percutaneous Angioembolization Before Esophagectomy in Patients With a High Risk of Anastomotic Leak
Led by Memorial Sloan Kettering Cancer Center · Updated on 2026-03-04
40
Participants Needed
7
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how often anastomotic leaks occur in patients who have esophageal cancer and are at high risk for these leaks. The study focuses on patients who are eligible for a procedure called gastric preconditioning by percutaneous angioembolization before they undergo esophagectomy, which is surgery to remove part or all of the esophagus. This research aims to better understand the risks associated with this approach in people with specific risk factors for leaks after surgery. Participants in this observational study will have gastric preconditioning using percutaneous angioembolization before their planned esophagectomy. The gastric preconditioning procedure is done prior to the esophagectomy to potentially reduce the risk of anastomotic leak. All participants will be people with esophageal malignancy who have a high risk of leakage and have agreed to receive this preconditioning. There are no requirements regarding prior treatments. During the study, researchers will monitor participants for the occurrence of anastomotic leaks for up to one year after surgery. They will collect information related to the surgery and outcomes to evaluate how often leaks happen in this high-risk group. Participants will be followed and assessed as part of routine care, with study data collected to understand the safety and incidence of leaks after this treatment approach. The total duration of follow-up is one year after the surgery.
CONDITIONS
Brief Title
Registry Study of People Who Are Having an Esophagectomy and Are at High Risk of Anastomotic Leak
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients must have pathologically confirmed esophageal malignancy requiring esophagectomy.
- Patients must have risk factors for anastomotic leak, including previous foregut or bariatric surgery (excluding fundoplication-only), salvage esophagectomy, planned cervical anastomosis, or two or more specified comorbidities.
- Patients must be candidates and have agreed to receive gastric preconditioning by percutaneous angioembolization before esophagectomy.
- Age 18 years or older.
- ECOG Performance Status of 2 or less.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 day for surgery
Participants undergo esophagectomy after preoperative gastric preconditioning by percutaneous angioembolization.
1 surgical procedure visit
Duration - Up to 1 year
Participants are monitored for up to 1 year to assess the incidence of anastomotic leak and recovery outcomes.
Periodic visits during follow-up as per clinical care
Trial Site Locations
Total: 7 locations
1
Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
Basking Ridge, New Jersey, United States, 07920
Actively Recruiting
2
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Middletown, New Jersey, United States, 07748
Actively Recruiting
3
Memorial Sloan Kettering Bergen (All Protocol Activities)
Montvale, New Jersey, United States, 07645
Actively Recruiting
4
Memorial Sloan Kettering Suffolk - Commack (All Protocol Activities)
Commack, New York, United States, 11725
Actively Recruiting
5
Memorial Sloan Kettering Westchester (All protocol activities)
Harrison, New York, United States, 10604
Actively Recruiting
6
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York, United States, 10065
Actively Recruiting
7
Memorial Sloan Kettering Nassau (All Protocol Activities)
Rockville Centre, New York, United States, 11553
Actively Recruiting
Research Team
D
Daniela Molena, MD
E
Ernesto Santos Martin, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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