Multicenter Randomized Controlled Trial for Application of Laparoscopic Total Gastrectomy With Lymph Node Dissection for Gastric Cancer (KLASS-06)

Who is this study for? Patients with proximal advanced gastric cancer
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Although Laparoscopic gastrectomy for both early and locally advanced gastric cancer has gained popularity, the use of laparoscopic total gastrectomy for proximal advanced gastric cancer is still limited to some experienced surgeons, because of its technical difficulties in D2 lymph node dissection and anastomoses. Some retrospective and cohort studies regarding laparoscopic total gastrectomy with lymph node dissection suggested the likelihood of application of laparoscopic surgery for proximal gastric cancer. However, there has been no randomized clinical trial comparing results of laparoscopic total gastrectomy with D2 lymph node dissection with open conventional surgery. Therefore, we aimed to verify the efficacy of laparoscopic total gastrectomy with D2(D2-10) lymph node dissection, technical and oncologic safety compared with open surgery via multicenter randomized clinical trial.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 80
Healthy Volunteers: f
View:

⁃ Patients who are over 20 and below 80 years old

⁃ Patients who have performance status of ECOG 0 or 1

⁃ Patients with American Society of Anesthesiology score of class I to III

⁃ Patients who are diagnosed with gastric adenocarcinoma not involving Z-line by endoscopy with biopsy

⁃ Patients with tumors which can be curatively resected by total gastrectomy with lymph node dissection based on preoperative study

⁃ Patients who have primary gastric carcinoma invaded into over muscle propria, and not into adjacent organ in preoperative studies (cT2 \

• cT4a)

⁃ Patients who have no metastasis to lymph nodes or limited metastasis to perigastric lymph node metastasis in preoperative studies (cN0 \

• cN2)

⁃ Patients who agree with participating in the clinical study with informed consents

⁃ Patients who can be followed for at least 3 years after study enrollment

Locations
Other Locations
Republic of Korea
Department of Surgery, Yonsei University College of Medicine, Seoul, Korea
RECRUITING
Seoul
Contact Information
Primary
Woo Jin Hyung, MD, PhD
wjhyung@yuhs.ac
+82-2-2228-2100
Time Frame
Start Date: 2018-04-05
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 772
Treatments
Experimental: Laparoscopic group
Arm Description: Laparoscopic radical total gastrectomy with D2 (or D2-#10) lymph node dissection
Active_comparator: Open group
Open radical total gastrectomy with D2 (or D2-#10) lymph node dissection
Sponsors
Leads: Yonsei University

This content was sourced from clinicaltrials.gov