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Clinical Trials in China / NCT05494086
Recruiting Not applicable

Dual-Port Laparoscopic Distal Gastrectomy for Gastric Cancer

NCT05494086 · tracked via the Priya Life Science China tracker
Sponsor
Nanfang Hospital, Southern Medical University
Phase
Not applicable
Started
2022-08-01
Last updated
2024-05-13

Condition(s) studied

Gastric Cancer

Investigational drug(s) / intervention(s)

DPLDGLDG

DPLDG: Dual-port laparoscopic distal gastrectomy

LDG: Laparoscopic distal gastrectomy

Study summary

Dual-port laparoscopic gastrectomy (DPLG) has been widely performed in recent years for treating gastric cancers. The present study explore the safety and effect of dual-port laparoscopic distal gastrectomy (DPLDG).

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: 1. patients within 18--75 years old; 2. patients with a preoperative pathological diagnosis of gastric adenocarcinoma; 3. patients with a clinical tumor stage of T1N1,T2N0 according to the preoperative examinations (gastroscopy, ultrasound gastroscopy and computed tomography); 4. patients with a plan to undergo laparoscopic distal gastrectomy and obtain R0 surgical results; 5. patients without severe heart, liver, lung, or kidney dysfunction; 6. patients with an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-1; and (7) patients with American Society of Anesthesiologists (ASA) I-II. Exclusion Criteria: 1. patients with a history of upperabdominal surgery; 2. patients who presentedas an emergency case; 3. patients with other histories of malignant diseases within 5 years; 4. patients with prior neoadjuvant chemotherapy or radiation therapy; and (5)patients who need simultaneous surgical treatment for other malignant diseases.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Nanfang Hospital Guangzhou Guangdong Recruiting

More Nanfang Hospital, Southern Medical University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05494086 on ClinicalTrials.gov ↗ ← All trials in China