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Application of modified proximal gastrectomy and digestive tract reconstruction based on gastric anatomy and physiology in proximal gastric and esophagogastric junction adenocarcinoma——A prospective, single-center, registration study

Application of modified proximal gastrectomy and digestive tract reconstruction based on gastric anatomy and physiology in proximal gastric and esophagogastric junction adenocarcinoma——A prospective, single-center, registration study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035692
Enrollment
Unknown
Registered
2020-08-16
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

gastric cancer

Interventions

observation group:modified proximal gastrectomy plus residual-gastroesophageal anastomosis
control group:total gastrectomy

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Histologically confirmed adenocarcinoma (biopsy by endoscopy before surgery); (2) The lesion is confined to the proximal 1/3 of the stomach, cT1-2N0M0 according to the AJCC (8th edition); or adenocarcinoma of the esophagogastric junction according to the Japanese Gastric Cancer Treatment Guideline (15th edition), and the length is less than 4 cm; (3) From 18 to 90 years old; (4) ECOG 0-2, ASA I-III; (5) Patients who received non-curative endoscopic surgery confirmed by pathology and need additional surgery can be included in this study; (6) Informed consent obtained; (7) Open surgery and laparoscopic surgery are both acceptable.

Exclusion criteria

Exclusion criteria: (1) Patient who received any anti-tumor treatment (chemotherapy, radiotherapy, targeted drug treatment, etc.) after being diagnosed with gastric cancer; (2) Patient who is participating in or has participated in other clinical studies in the past six months; (3) Vulnerable groups ; (4) Patient who suffers from a serious mental illness; (5) Patient who suffers from other malignant tumors within five years; (6) Pregnant women, lactating women, and those planning to become pregnant.

Design outcomes

Primary

MeasureTime frame
the incidence of reflux esophagitis within postoperative 1 year;

Secondary

MeasureTime frame
Symptoms of esophageal reflux;postoperative quality of life;complications of surgery;nutritional status;oncological efficacy;

Countries

China

Contacts

Public ContactSHU PING

Zhongshan Hospital, Fudan University

shuping2007@aliyun.com+86 15900525744

Outcome results

None listed

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