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Clinical Trials/NCT05541783
NCT05541783CompletedNot Applicable

A Multi-center Prospective Randomized Controlled Trial Comparing the Quality of Life Between Laparoscopic-assisted Distal Gastrectomy (LADG) and Totally Laparoscopic Distal Gastrectomy (TLDG) for Gastric Cancer

Fudan University2 sites in 1 country213 target enrollmentStarted: September 15, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
213
Locations
2
Primary Endpoint
Scores on the physical function and pain symptom scales of EORTC QLQ-C30 questionnaire

Study Overview

Brief Summary

The aim of this study is comparing the short-term quality of life between laparoscopy-assisted distal gastrectomy and totally laparoscopic distal gastrectomy for gastric cancer.

Detailed Description

Although totally laparoscopic distal gastrectomy (TLDG) and laparoscopic-assisted distal gastrectomy (LADG) are both minimally invasive surgeries for gastric cancer with the same surgical treatment principles, in the former, all surgical processes are performed intracorporeally, while, in the latter, extracorporeal gastro-enteric anastomosis is achieved. Whether the procedural differences between TLDG and LADG affect quality of life (QOL)is still under debate.To evaluate how each laparoscopic surgery affect QOL of patients with gastric cancer, it is necessary to compare the postoperative QOL (scoring by questionnaire) between the patients undergoing TLDG and LADG through a multi-center randomized controlled trial.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Aged 20-80 years;
  • •Patients had an Eastern Cooperative Oncology Group performance status score of 0 or 1;
  • •Patients had histologically confirmed gastric adenocarcinoma (tumor size<5cm) at clinical stage I-III with T1-4aN0-2M0 excluding T4b or N3 tumors, according to the of the American Joint Committee on Cancer classification system, eighth edition;
  • •Patients were expected to undergo laparoscopic distal gastrectomy with D2 lymphadenectomy.

Exclusion Criteria

  • •Patients had bulky regional lymph nodes (larger than 3 cm at the long diameter) or possible distant metastasis in preoperative evaluation
  • •Patients had history of chemotherapy, radiotherapy, immunotherapy or target therapy;
  • •Patients had any concurrent or previous malignant tumor;
  • •Patients had unstable cardiovascular, respiratory, kidney, or liver disease and poorly controlled hypertension, diabetes, mental disorders; history of upper abdominal surgery (except laparoscopic cholecystectomy).
  • •Patients were histologically proven gastric adenocarcinoma (by preoperative gastrofiberscopy).

Arms & Interventions

Totally laparoscopic distal gastrectomy

Experimental

The patients who are allocated to TLDG group undergo intracorporeal anastomosis for the recovery of gastrointes- tinal continuity after gastrectomy.

Intervention: Totally laparoscopic distal gastrectomy (Procedure)

Laparoscopy-assisted distal gastrectomy

Active Comparator

The patients who are assigned to LADG group undergo extracorporeal anasto- mosis for gastrointestinal reconstruction.

Intervention: laparoscopy-assisted distal gastrectomy Group (Procedure)

Outcomes

Primary Outcomes

Scores on the physical function and pain symptom scales of EORTC QLQ-C30 questionnaire

Time Frame: 30 days postoperatively

Scores on the physical function and pain symptom scales of EORTC QLQ-C30 questionnaire at 30 days postoperatively

Secondary Outcomes

  • hospital stay cost(30-day)
  • Intraoperative and postoperative morbidities and mortality(90-day)
  • Scores on the other scales of EORTC QLQ-C30 questionnaire postoperatively(30 days postoperatively)
  • Scores on EORTC QLQ-C30 questionnaire(7 days and 90 days postoperatively)
  • Scores on the scales of EORTC QLQ-STO22 questionnaire postoperatively(7,30 and 90 days postoperatively)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dazhi Xu

PHD,MD

Fudan University

Study Sites (2)

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