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Prospective, Multicenter, Single-Arm Clinical Study on the Application of Single-Port Laparoscopic Endoscopic Surgery System in Radical Gastrectomy for Gastric Cancer

Prospective, Multicenter, Single-Arm Clinical Study on the Application of Single-Port Laparoscopic Endoscopic Surgery System in Radical Gastrectomy for Gastric Cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106846
Enrollment
Unknown
Registered
2025-07-30
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

gastric cancer

Interventions

Single-port robotic surgery group:Perform Single-port robotic surgery

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age >=18 years and =80 years, no gender restriction; (2) BMI: 18–25 kg/m^2; (3) Clinical stage of gastric cancer: cT1-3N0-1M0, requiring radical gastrectomy; (4) Physically eligible for laparoscopic surgery; (5) Willing to comply with study follow-up and required examinations; (6) Voluntary signing of informed consent form.

Exclusion criteria

Exclusion criteria: (1) Severe cardiovascular or circulatory system diseases with inability to tolerate surgery; (2) Pregnancy or lactation; (3) History of epilepsy or psychiatric disorders that are uncontrolled; (4) Previous surgical history at the relevant operative site; (5) Severe allergic constitution, or suspected/confirmed alcohol or drug addiction; (6) Intra-abdominal infection, peritonitis, diaphragmatic hernia, severe systemic infection, or metastatic disease; (7) Inability to comprehend study requirements or complete follow-up assessments; (8) Other conditions deemed ineligible by investigators (e.g., unwillingness to comply with the study protocol, unrealistic expectations, or significant emotional/psychological issues).

Design outcomes

Primary

MeasureTime frame
Operation efficiency;

Secondary

MeasureTime frame
Complications incidence;Adverse event rate;

Countries

China

Contacts

Public ContactXian Shen

The First Affiliated Hospital of Wenzhou Medical University

13968888872@163.com+86 139 6888 8872

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026