Clinical Efficacy Between Robotic and Laparoscopic Total Gastrectomy in Patients With Clinical Stage I Gastric Cancer

Sponsor
Fujian Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03524300
Collaborator
(none)
220
1
2
78
2.8

Study Details

Study Description

Brief Summary

The purpose of this study is to explore the clinical efficacy between robotic and laparoscopic total gastrectomy in patients with clinical Stage I gastric cancer

Condition or Disease Intervention/Treatment Phase
  • Procedure: Robotic Assisted Total Gastrectomy
  • Procedure: Laparoscopic Assisted Total Gastrectomy
N/A

Detailed Description

Robotic surgery has been developed with the aim of improving surgical quality and overcoming the limitations of conventional laparoscopy in the performance of complex mini-invasive procedures. The study is designed to explore the clinical outcomes of the robotic assisted total gastrectomy by comparing short- and long-term outcomes including financial cost of robotic and laparoscopic assisted total gastrectomy in the treatment of clinical Stage I gastric adenocarcinoma (cStage IA(T1N0M0)or cStage IB(T1N1M0,T2N0M0)).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
220 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective Randomized Controlled Trial for Comparison of Clinical Efficacy Between Robotic and Laparoscopic Total Gastrectomy in Patients With Clinical Stage I Gastric Cancer
Actual Study Start Date :
Jun 1, 2018
Anticipated Primary Completion Date :
Nov 30, 2021
Anticipated Study Completion Date :
Nov 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Robotic Assisted Total Gastrectomy

Robotic Assisted Total Gastrectomy will be performed for the treatment of patients assigned to this group.

Procedure: Robotic Assisted Total Gastrectomy
After exclusion of T4b, bulky lymph nodes, or distant metastasis case,robotic assisted total gastrectomy will be performed in the experimental group.

Active Comparator: Laparoscopic Assisted Total Gastrectomy

Laparoscopic Assisted Total Gastrectomy will be performed for the treatment of patients assigned to this group.

Procedure: Laparoscopic Assisted Total Gastrectomy
After exclusion of T4b, bulky lymph nodes, or distant metastasis case,laparoscopic assisted total gastrectomy will be performed in the experimental group.

Outcome Measures

Primary Outcome Measures

  1. 3-year disease free survival rate [36 months]

    the rate of 3-year disease free survival

Secondary Outcome Measures

  1. 3-year overall survival rate [36 months]

    the rate of 3-year overall survival rate

  2. 3-year recurrence pattern [36 months]

    the pattern of recurrence in 3 years

  3. overall postoperative morbidity rates [30 days]

    Refers to the incidence of early postoperative complications. The early postoperative complication are defined as the event observed within 30 days after surgery.

  4. intraoperative morbidity rates [1 day]

    The intraoperative postoperative morbidity rates are defined as the rates of event observed within operation.

  5. overall postoperative serious morbidity rates [30 days]

    Refers to the incidence of early postoperative complication which is graded as Clavien-Dindo IIIA or higher.

  6. Time to first ambulation [30 days]

    Time to first ambulation in hours is used to assess the postoperative recovery course.

  7. Time to first flatus [30 days]

    Time to first flatus in days is used to assess the postoperative recovery course.

  8. Time to first liquid diet [30 days]

    Time to first liquid diet in days is used to assess the postoperative recovery course

  9. Time to first soft diet [30 days]

    Time to first soft diet in days is used to assess the postoperative recovery course.

  10. Duration of postoperative hospital stay [30 days]

    Duration of postoperative hospital stay in days is used to assess the postoperative recovery course.

  11. The variation of weight [3, 6, 9 and 12 months]

    The variation of weight in kilograms on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status.

  12. The variation of white blood cell count [Preoperative 3 days and postoperative 1, 3, and 5 days]

    The values of white blood cell count from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory response.

  13. Hospitalization expenses [30 days]

    The cost from admission to discharge

  14. operation time [1 day]

    operation time

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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 cStage IA(T1N0M0)or cStage IB(T1N1M0,T2N0M0)at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual 8th Edition

  • The tumor is on the upper or middle third stomach and expected to perform total gastrectomy with D1+/D2-10 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:
  • cStage IIA or more advaned at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual 8th Edition

  • Women during pregnancy or breast-feeding

  • Severe mental disorder

  • History of previous upper abdominal surgery (except laparoscopic cholecystectomy)

  • Multiple primary cancer

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fujian Medical University Union Hospital Fuzhou Fujian China 350000

Sponsors and Collaborators

  • Fujian Medical University

Investigators

  • Principal Investigator: Changming Huang, Professor, Fujian Medical University Union Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Chang-Ming Huang, Prof., Director, Head of gastric surgery, Principal Investigator, Clinical Professor, Fujian Medical University
ClinicalTrials.gov Identifier:
NCT03524300
Other Study ID Numbers:
  • FUGES-015
First Posted:
May 14, 2018
Last Update Posted:
Feb 5, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Chang-Ming Huang, Prof., Director, Head of gastric surgery, Principal Investigator, Clinical Professor, Fujian Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 5, 2020