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Upper cardia esophagus mucosa and submucosa loop resection then coincide joint pericardial blood vessel amputation surgery in treatment of gastroesphageal variceal hemorrhage

Upper cardia esophagus mucosa and submucosa loop resection then coincide joint pericardial blood vessel amputation surgery in treatment of gastroesphageal variceal hemorrhage

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13004185
Enrollment
Unknown
Registered
2014-01-21
Start date
2014-02-01
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

Gastroesphageal variceal hemorrhage

Interventions

The experimental group:Above the cardia esophagus mucosa and submucosa loop resection then coincide joint pericardial blood vessel amputation surgery
The control group:Pericardial blood vessel amputation surgery

Sponsors

the 175th Hospital of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. cirrhotic patients with acute or recent (within 3 months) esophageal or gastric variceal hemorrhage; 2. cirrhotic patients was confirmed with the laboratory and imageology data; 3. the degree of gastroesophageal varices was F2 or F3 in these patients, as revealed by gastroendoscopy; 4. computerized tomography (CT) portal venography was performed for detection of variceal afferent veins before operation; 5. giving the consent to complete Preoperative check and postoperative recheck.

Exclusion criteria

Exclusion criteria: 1. association with hepatocellular carcinoma or other malignancy; 2. complete obstruction of the portal vein due to thrombosis; 3. grave hypertension, coronary heart disease, or impaired function of cardiorespiratory; 4. encephalopathy greater than stage II; severe jaundice with serum bilirubin more than 100 mg L-1; 5. presence of hepato-renal syndrome or chronic renal insufficiency; 6. obvious hemorrhagic tendency, PT>25s; 7. The portal vein was failure to venous cannula with kinds of cause; 8. inability or refusal to give the consent to complete preoperative check and postoperative recheck.

Design outcomes

Primary

MeasureTime frame
Routine hematology;Liver function;Blood dynamic indicators of post-operation;Difference between free portal vein pressure before operation and mesenteric area presure after operation;Spleen size;Kidney function;

Countries

China

Contacts

Public ContactJing Liu

the 175th Hospital of PLA

liujdoctor@hotmail.com+86 13386966271

Outcome results

None listed

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