Skip to content

Prospective clinical trial on the long-term outcome and survival of vagus (coeliac branch)-preserving gastrectomy for cT1-3 gastric cancer

Prospective clinical trial on the long-term outcome and survival of vagus (coeliac branch)-preservin

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14005216
Enrollment
Unknown
Registered
2014-09-03
Start date
2014-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

gastric cancer

Interventions

Sponsors

the 1st Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 70 years old, with the diagnosis of gastric cancer confirmed by pathological methods, cT1-3 stage and the region of gastric cancer is suitable for distal gastrectomy; 2. No diabetes and other metabolic disorders, no internal or surgical diseases that can influence the nutrition digestion, absorption and metabolism; 3. No contraindications for anesthesia and surgery; 4. No hematological disorders that can influence hemoglobin level postoperation; 5. Perform radical surgery for gastric cancer (D2) and confirm that no gross residual cancer; T1-3 stage gastric cancer confirmed by pathological methods postoperative, dissection of lymph nodes more than 15; 6. No therapy that may influence the gastrointestinal function and movement, such as intraperitoneal chemotherapy or heat therapy; no other abdominal surgery during the study except total gastrectomy and digestive tract reconstruction;7. The inclusion of patients should be discussed by doctors of the department, and the inclusion should be confirmed by two doctors at least; 8. Sign informed contents.

Exclusion criteria

Exclusion criteria: 1. Cancer recurrence, metastasis or patients die during the study; 2. Patients are not willing to participate in the study; 3. Pregnant females.

Design outcomes

Primary

MeasureTime frame
Parameters of the surgery;Quality of life;Nutrition parameter;

Countries

China

Contacts

Public ContactXiang Hu
caoliang913@163.com+86 13332265588

Outcome results

None listed

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