A Observational Study to Compare Effectiveness and Safety of the Surgeries in Patients With Esophageal Cancer

Chinese PLA General Hospital (301 Hospital)

Status

Completed

Conditions

Esophageal Cancer

Treatments

Procedure: Surgeries

Study type

Observational

Funder types

Other

Industry

Identifiers

NCT03428074

301-EC-01

Details and patient eligibility

About

The study was designed to compare effectiveness and safety of the surgeries of Ivor-Lewis and Mckeown in patients with esophageal cancer

Full description

The trial is a multi-centre real-world non-interventional observational study. The study was designed to compare effectiveness and safety of the minimally invasive surgeries of Ivor-Lewis and Mckeown in the Chinese patients with IA-IIIB esophageal cancer via a retrospectively review method based on the study data on patient demographic/tumor biological characteristics and clinical treatments.

Enrollment

1,862 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Pathologically diagnosed middle and lower thoracic IA-IIIB esophageal cancer after surgeries;
Patients who received minimally invasive radical dissections of Ivor-Lewis and Mckeown;
Patients who received tubular gastroesophageal reconstruction;

Exclusion criteria

Patients complicated with arrhythmia, or serious disfunctions of heart, lung, liver, and kidney before surgeries;
Patients with second primary tumors;
Patients who received abdominal or thoracic surgeries;
Patients who received gastrostomy or nesteostomy before surgeries;
Patients with suspected cervical lymph metastases (in the subgroup of the patients who received the surgery of Mckeown)