Assessing the feasibility and safety of robotic-assisted proximal gastrectomy with double-flap technique for proximal early gastric cancer: study protocol for a phase II, multicentre, single-arm clinical trial.
기술보고
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: reflux oesophagitis (Los Angeles Grade B or more) within 12 months postoperatively
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
We will report the findings in international peer-reviewed journals. [TRIAL REGISTRATION NUMBER] NCT05892289.
[INTRODUCTION] Robotic-assisted proximal gastrectomy with double flap technique (RPG-DFT) reconstruction has been used to treat proximal early gastric cancer and reconstruct the digestive tract in rec
APA
Zhong G, Xie Y, et al. (2025). Assessing the feasibility and safety of robotic-assisted proximal gastrectomy with double-flap technique for proximal early gastric cancer: study protocol for a phase II, multicentre, single-arm clinical trial.. BMJ open, 15(8), e094661. https://doi.org/10.1136/bmjopen-2024-094661
MLA
Zhong G, et al.. "Assessing the feasibility and safety of robotic-assisted proximal gastrectomy with double-flap technique for proximal early gastric cancer: study protocol for a phase II, multicentre, single-arm clinical trial.." BMJ open, vol. 15, no. 8, 2025, pp. e094661.
PMID
40789587 ↗
Abstract 한글 요약
[INTRODUCTION] Robotic-assisted proximal gastrectomy with double flap technique (RPG-DFT) reconstruction has been used to treat proximal early gastric cancer and reconstruct the digestive tract in recent years. However, due to the complexity of this surgical procedure, all of the reports were retrospective. The application of RPG-DFT in the context of proximal early gastric cancer remains a nascent area of investigation. Large-scale, prospective trials are necessary to assess the feasibility and safety of RPG-DFT for proximal early gastric cancer.
[METHODS AND ANALYSIS] This study is a phase II, multicentre, single-arm clinical trial that investigates the feasibility and safety of RPG-DFT for proximal early gastric cancer. A total of 42 eligible patients who met the inclusion criteria will be allocated to the RPG-DFT group. General and clinical data will be collected at the time of patient enrolment and maintained in accordance with the patient's progress throughout their medical and follow-up care. The primary endpoint is the proportion of patients with reflux oesophagitis (Los Angeles Grade B or more) within 12 months postoperatively. The secondary endpoints included intraoperative outcomes, postoperative recovery, postoperative pain assessment, pathological outcomes, postoperative quality of life, postoperative nutritional status, morbidity and mortality rate.
[ETHICS AND DISSEMINATION] The protocol was approved by the Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Ethics Committee (registration number: SYSKY-2022-275-02) on 28 September 2022. We will report the findings in international peer-reviewed journals.
[TRIAL REGISTRATION NUMBER] NCT05892289.
[METHODS AND ANALYSIS] This study is a phase II, multicentre, single-arm clinical trial that investigates the feasibility and safety of RPG-DFT for proximal early gastric cancer. A total of 42 eligible patients who met the inclusion criteria will be allocated to the RPG-DFT group. General and clinical data will be collected at the time of patient enrolment and maintained in accordance with the patient's progress throughout their medical and follow-up care. The primary endpoint is the proportion of patients with reflux oesophagitis (Los Angeles Grade B or more) within 12 months postoperatively. The secondary endpoints included intraoperative outcomes, postoperative recovery, postoperative pain assessment, pathological outcomes, postoperative quality of life, postoperative nutritional status, morbidity and mortality rate.
[ETHICS AND DISSEMINATION] The protocol was approved by the Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Ethics Committee (registration number: SYSKY-2022-275-02) on 28 September 2022. We will report the findings in international peer-reviewed journals.
[TRIAL REGISTRATION NUMBER] NCT05892289.
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