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Randomized Controlled Trials on Laparoscopic No. 14v LNS Dissection

Randomized Controlled Trials on Laparoscopic No. 14v Lymph Node Dissection for Advanced Lower Third Gastric Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02789891
Enrollment
326
Registered
2016-06-03
Start date
2016-06-30
Completion date
2024-01-31
Last updated
2020-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stomach Neoplasms

Brief summary

The purpose of this study is to explore the short-term, long-term and oncological outcomes of laparoscopic No. 14v lymph node dissection in advanced lower third gastric cancer.

Detailed description

A prospective randomized comparison of laparoscopic No. 14v lymph node dissection in advanced lower third gastric cancer will be performed, to evaluate the short-term, long-term and oncological outcomes. The evaluation parameters are perioperative clinical efficacy, postoperative life quality, immune function and 3-year survival and recurrence rates.

Interventions

PROCEDURED2 lymphadenectomy including No. 14v

After exclusion of T4b, or distant metastasis case by diagnostic laparoscopy, Laparoscopic distal with D2 lymphadenectomy including No. 14v Lymph Node Dissection will be performed with curative treated intent. The type of reconstruction will be selected according to the surgeon's experience

PROCEDURElymphadenectomy excluding No. 14v

After exclusion of T4b, or distant metastasis case by diagnostic laparoscopy, Laparoscopic distal gastrectomy with D2 lymphadenectomy excluding No. 14v Lymph Node Dissection will be performed with curative treated intent. The type of reconstruction will be selected according to the surgeon's experience

Sponsors

Fujian Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
10 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

• Age from 18 to 75 years * Primary lower third gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy * cT2-4a, N0-3, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual Seventh Edition * No distant metastasis is observed. And the spleen, pancreas or other adjacent organs are not involved by the tumor. * Performance status of 0 or 1 on Eastern Cooperative Oncology Group scale (ECOG) * American Society of Anesthesiology score (ASA) class I, II, or 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 gastrectomy, endoscopic mucosal resection or endoscopic submucosal dissection * Enlarged or bulky regional lymph node envelop important vessels * History of other malignant disease within past five years * History of previous neoadjuvant chemotherapy or radiotherapy * History of unstable angina or myocardial infarction within past six months * History of cerebrovascular accident within past six months * History of continuous systematic administration of corticosteroids within one month * Requirement of simultaneous surgery for other disease * Emergency surgery due to complication (bleeding, obstruction or perforation) caused by gastric cancer * FEV1\<50% of predicted values

Design outcomes

Primary

MeasureTime frame
3-year disease overall survival rate36 months

Secondary

MeasureTime frameDescription
The number of positive lymph nodes1 day
No.14v Lymph node metastasis rate10 days
Morbidity and mortality30 days; 36 monthsThe early postoperative complication and mortality are defined as the event observed within 30 days after surgery, while the time frame for late complication is the period from postoperative day 31th to the end of month 36th.
3-year free survival rate36 months
3-year recurrence pattern36 monthsRecurrence patterns are classified into five categories at the time of first diagnosis: locoregional, hematogenous, peritoneal, distant lymph node, and mixed type
Time to first ambulation10 daysThe data of postoperative recovery course.
The number of lymph node dissection10day
The variation of weight12 monthsThe variation of weight on postoperative 3, 6, 9 and 12 months
The daily highest body temperature7 dayThe daily highest body temperature before discharge
Time to first flatus10 days
Time to first liquid diet10 days
Time to soft diet10 days
Duration of hospital stay10 days
The amount of abdominal drainage10 days
Blood transfusion10 days
Intraoperative blood loss1 day
Intraoperative injury1 day
The amount of use of titanium clip1 day
The rate of conversion to laparotomy1 day
The variation of cholesterol12 monthsThe variation of cholesterol on postoperative 3, 6, 9 and 12 months
The variation of albumin12 monthsThe variation of albumin on postoperative 3, 6, 9 and 12 months
The results of endoscopy12 monthsthe results of endoscopy on postoperative 3 and 12 months
The values of white blood cell count7 daysthe values of white blood cell count from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded
The values of hemoglobin7 daysand the values of hemoglobin from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded.
The values of C-reactive protein7 daysand the values of C-reactive protein from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded.
The values of prealbumin7 daysand the values of prealbumin from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded.
The values of relevant immune cytokines7 daysand the values of relevant immune cytokines including T cell percentage, T-helper lymphocytes (CD4+) percentage, T-suppressor lymphocytes (CD8+) percentage, natural killer (NK) cells percentage from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded.
Visual Analog Score for pain7 daysthe values of visual analog score for pain before operation and on postoperative day 1 to day 7 are recorded.
EORTC QLQ-C30 and QLQ - STO22Time Frame: 36 monthsEuropean Organization fo Research and Treatment(EORTC) QLQ-C30 and QLQ - STO22 before operation and on postoperative month 6,12,36 are recorded.
Intraoperative lymph node dissection time1 dayintraoperative No.14v lymph node dissection time includes infrapyloric area lymph node,suprapancreatic area lymph node,splenic hilar area lymph node, cardial area lymph node

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026