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Clinical study of laparoscopic modified Overlap anastomosis in digestive tract reconstruction after resection of Siewert ? and ? esophagogastric junction adenocarcinoma

Clinical study of laparoscopic modified Overlap anastomosis in digestive tract reconstruction after resection of Siewert ? and ? esophagogastric junction adenocarcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068882
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Adenocarcinoma of esophagogastric junction

Interventions

Experimental group:Laparoscopic modified Overlap anastomosis
Verification group:Laparoscopic circular stapled anastomosis

Sponsors

The second Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Physical condition and visceral function allow to undergo major abdominal surgery; (2) Be able to abide by the protocol during the study and sign written informed consent before entering the study screening; (3) Patients aged 18-80 years with gastric adenocarcinoma confirmed by pathology before operation; (4) The expected survival period is>6 months; (5) No other serious concomitant diseases and good organ function; (6) There are no medical contraindications that seriously affect anesthesia and surgery; (7) All patients did not receive adjuvant radiotherapy and chemotherapy before operation; (8) The 8th AJCC stage is T2-4aNxM0 gastric cancer patients; (9) No history of upper abdominal surgery; No history of peritonitis and pancreatitis; (10) Postoperative patients can undergo 6-8 cycles of XELOX chemotherapy.

Exclusion criteria

Exclusion criteria: (1) Age = 80 years old; (2) There are serious complications affecting the quality of life; (3) Combined with other organ resection; (4) Palliative operation and emergency operation due to digestive tract perforation, obstruction and bleeding;

Design outcomes

Primary

MeasureTime frame
Postoperative complication;

Secondary

MeasureTime frame
Intraoperative blood loss volume;operative time;Number of dissected lymph nodes;Incision length;Postoperative ventilation time;Postoperative feeding time;Postoperative hospitalization;Hospitalization expenses;

Countries

China

Contacts

Public ContactFan Yong

The second Hospital of Lanzhou University

fanyong1972@163.com+86 138 9335 2059

Outcome results

None listed

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