Skip to content

Prospective clinical trial on different strategies of digestive tract reconstruction after total gastrectomy

Prospective clinical trial on different strategies of digestive tract reconstruction after total gastrectomy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000785
Enrollment
Unknown
Registered
2010-01-10
Start date
2009-04-01
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

1:Hao's treatment+Pouch operation
2:Roux-en-Y+Pouch
3:Roux-en-Y
4:Hao's operation

Sponsors

Cancer Hospital of Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
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, and the region of gastric cancer is suitable for total 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. Confirm that the region of gastric cancer is suitable for total gastrectomy and gastric cancer is of II or IIIA stage during surgery (6th version AJCC, 2002); 6. Perform radical surgery for gastric cancer (=15; 7. No therapy that may influence the gastrointestinal function and movement, such as intraperitoneal chemotherapy or heat therapy; 8. No other abdominal surgery during the study except total gastrectomy and digestive tract reconstruction; 9. The inclusion of patients should be discussed by doctors of the department, and the inclusion should be confirmed by two doctors at least; 10. 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;

Contacts

Public ContactHan Liang
zale329@yahoo.com.cn+86 13820182495

Outcome results

None listed

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