Esophagogastric Junction Adenocarcinoma Clinical Trial
Official title:
Randomized Controlled Trials on Clinical Outcomes of Robotic Versus Laparoscopic Assisted Radical Gastrectomy for Advanced Siewert II/III Esophagogastric Junction Adenocarcinoma
Verified date | February 2020 |
Source | Fujian Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to explore the clinical outcomes of the robotic assisted radical gastrectomy for advanced Siewert II/III esophagogastric junction adenocarcinoma(cT2-4a, N-/+, M0)
Status | Enrolling by invitation |
Enrollment | 300 |
Est. completion date | October 2025 |
Est. primary completion date | October 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Age from over 18 to under 75 years - Primary gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy - cT2-4a(clinical stage tumor), N-/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual 8th Edition - Expected to perform total gastrectomy with D2+No.19+No.20 lymph node dissction to obtain R0 resection sugicall results. - Performance status of 0 or 1 on ECOG (Eastern Cooperative Oncology Group) scale - ASA (American Society of Anesthesiology) class I to III - Written informed consent Exclusion Criteria: - Women during pregnancy or breast-feeding - Severe mental disorder - History of previous upper abdominal surgery (except laparoscopic cholecystectomy) - History of previous gastric surgery (except ESD/EMR (Endoscopic Submucosal Dissection/Endoscopic Mucosal Resection )for gastric cancer) - Gastric multiple primary carcinoma - Enlarged or bulky regional lymph node (diameter over 3cm)supported by preoperative imaging - History of other malignant disease within the past 5 years - History of previous neoadjuvant chemotherapy or radiotherapy - History of unstable angina or myocardial infarction within the past 6 months - History of cerebrovascular accident within the past 6 months - History of continuous systematic administration of corticosteroids within 1 month - Requirement of simultaneous surgery for other disease - Emergency surgery due to complication (bleeding, obstruction or perforation) caused by gastric cancer - FEV1<50% of the predicted values |
Country | Name | City | State |
---|---|---|---|
China | Fujian Medical University Union Hospital | Fuzhou | Fujian |
Lead Sponsor | Collaborator |
---|---|
Fujian Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 3-year disease free survival rate | 3-year disease free survival rate | 36 months | |
Secondary | 3-year overall survival rate | 3-year overall survival rate | 36 months | |
Secondary | 3-year recurrence pattern | 3-year recurrence pattern | 36 months | |
Secondary | overall postoperative morbidity rates | overall postoperative morbidity rates | 30 days | |
Secondary | intraoperative morbidity rates | intraoperative morbidity rates | 1 day | |
Secondary | overall postoperative serious morbidity rates | overall postoperative serious morbidity rates | 30 days | |
Secondary | number of retrieved lymph nodes | number of retrieved lymph nodes | 14 days | |
Secondary | Time to first ambulation | Time to first ambulation is used to access the postoperative recovery course. | 30 days | |
Secondary | Time to first flatus | Time to first flatus is used to access the postoperative recovery course. | 30 days | |
Secondary | Time to first liquid diet | Time to first liquid diet is used to access the postoperative recovery course. | 30 days | |
Secondary | Time to soft diet | Time to soft diet is used to access the postoperative recovery course. | 30 days | |
Secondary | Duration of hospital stay | Duration of hospital stay is used to access the postoperative recovery course. | 30 days | |
Secondary | The amount of abdominal drainageare | The amount of abdominal drainageare is used to access the postoperative recovery course. | 30 days | |
Secondary | postoperative nutritional status | Weight and height will be combined to report BMI in kg/m^2. The variation of BMI in kg/m^2 on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status. | 3, 6, 9 and 12 months | |
Secondary | Hospitalization costs | Hospitalization costs | 30 days |
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