Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT04443478

Laparoscopic Versus Open Lower Mediastinal Lymphadenectomy for Esophagogastric Junction Cancer

Led by Peking University · Updated on 2021-12-02

1036

Participants Needed

1

Research Sites

308 weeks

Total Duration

On this page

Sponsors

P

Peking University

Lead Sponsor

P

Peking University Cancer Hospital & Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

Mediastinal lymph node dissection has been adopted as standard treatment for adenocarcinoma of esophagogastric junction(AEJ). This multi-center, exploratory, prospective, cohort study aims at provide standard technical details of laparoscopic mediastinal lymph node dissection, and explore the potential clinical effects, gather key information for following study regarding sample size calculation, primary outcome and feasibility.

CONDITIONS

Official Title

Laparoscopic Versus Open Lower Mediastinal Lymphadenectomy for Esophagogastric Junction Cancer

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years
  • Karnofsky score of 70% or higher, or ECOG score of 2 or less
  • Pathological biopsy confirming adenocarcinoma
  • Tumor centered within 5cm above or below the esophagogastric junction crossing or touching the junction
  • Esophageal invasion length of 2cm or less
  • Clinical cancer stage CT2-4aN0-3M0 by abdominal contrast-enhanced CT or MRI
  • Blood tests meeting specified hemoglobin, neutrophil, platelet, liver and kidney function levels
  • Signed informed consent obtained
Not Eligible

You will not qualify if you...

  • Prior anti-cancer treatment before surgery
  • Multiple malignant tumors in the stomach
  • Suspicious lymph node metastasis in middle or upper mediastinum
  • History of upper abdominal surgery (except laparoscopic cholecystectomy)
  • Pregnant or breastfeeding women
  • Uncontrolled epilepsy, central nervous system disease, or mental disorder
  • Bulky N2 lymph node status
  • Emergency surgery cases
  • Severe heart disease
  • Cerebral infarction or hemorrhage within past 6 months
  • Organ transplant recipients requiring immunosuppressive therapy
  • Other malignancies diagnosed within 5 years (except cured dermoid cancer and cervical cancer)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beijing Cancer Hospital

Beijing, Beijing Municipality, China, 100142

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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