esophageal cancer
Conditions
Interventions
Control group:Routine endoscopic rod dilation
Experimental group:Conventional endoscopic rod dilation + postoperative anastomotic injection of PRP
Sponsors
The Affiliated Hospital of Southwest Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. The patient has subjective symptoms of dysphagia after radical resection of esophageal cancer, such as only liquid diet; 2. Aged 18-80 years; 3. There is no contraindication for endoscopic treatment, and ordinary gastroscope cannot pass through the stenosis smoothly; 4. No local recurrence or peripheral invasion confirmed by imaging; 5. Patients and their families gave informed consent to this study and signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with other malignant tumors or other esophageal diseases; 2. Complicated with organ dysfunction; 3. Combined with anastomotic leakage; 4. Patients with recurrence of anastomotic tumor; 5. Those with poor treatment compliance and unable to complete the follow-up review; 6. Pregnant or lactating patients.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dysphagia score;Times of dilatation;Incidence of stricture;Duration of remission of stricture symptoms;Diameter of anastomosis under gastroscope; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of postoperative complications: chest pain, infection, perforation, bleeding, etc; | — |
Countries
China
Contacts
Public ContactShi Lei
The Affiliated Hospital of Southwest Medical University
Outcome results
None listed