Esophageal Cancer Clinical Trial
— PLACE020Official title:
Porcine Fibrin Sealant in Preventing Cervical Anastomotic Leakage After Esophagectomy for Esophageal or Junctional Carcinoma: A Phase II,Single Arm,Prospective Study.
Verified date | August 2021 |
Source | Sun Yat-sen University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary objective is to evaluate the efficacy and assess the role of Porcine Fibrin Sealant (Bioseal®) in preventing cervical anastomotic leakage after esophagectomy in the patients with resectable thoracic esophageal cancer and gastroesophageal junction cancer.
Status | Completed |
Enrollment | 57 |
Est. completion date | August 22, 2021 |
Est. primary completion date | March 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. Histologic diagnosis of squamous cell carcinoma or adenocarcinoma of thoracic esophageal carcinoma or gastroesophageal junction cancer with Stage T1-4aN0-3M0, according to 8th edition of Union for International Cancer Control (UICC) staging system 2. More than 6 months of expected survival 3. Age ranges from 18 to 80 years 4. Absolute white blood cells count =4.0×109/L, neutrophil =1.5×109/L, platelets =100.0×109/L, hemoglobin =90g/L, and normal functions of liver and kidney. 5. WHO performance status (PS) of 0-1 6. Informed consent will be obtained before the study Exclusion Criteria: 1. Patients who have undergone definitive chemoradiotherapy 2. Patients with concomitant hemorrhagic disease 3. Patients with other uncontrollable status that cannot tolerate surgery 4. Patients with known hypersensitivity to the porcine fibrin sealant product 5. Pregnant or breast feeding 6. Patients cannot signed the informed consent document because of psychological quality, family and social factors 7. Patients with concomitant peripheral neuropathy, whose CTC status is 2 or even more 8. Have a history of diabetes over 10 years and with poorly controlled blood sugar level 9. Patients with serious cardiac, respiratory, hepatic, renal,hematologic, immunological disease or cachexy, who cannot tolerate surgery |
Country | Name | City | State |
---|---|---|---|
China | Sun Yat-sen University Cancer Center | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Sun Yat-sen University |
China,
Chen W, Zheng R, Baade PD, Zhang S, Zeng H, Bray F, Jemal A, Yu XQ, He J. Cancer statistics in China, 2015. CA Cancer J Clin. 2016 Mar-Apr;66(2):115-32. doi: 10.3322/caac.21338. Epub 2016 Jan 25. — View Citation
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of postoperative cervical anastomotic leakage | Cervical anastomotic leakage will be diagnosed based on a combination of clinical presentation, radiological findings, and/or endoscopic findings within the first 3 months after the operation. | within the first 3 months after esophagectomy | |
Secondary | Overall survival | Overall survival (OS) is defined as the time period from the date of enrollment to the date of death or the last follow up | At end of trial- up to 2 years in follow up | |
Secondary | Disease Free Survival | Disease-free survival (DFS) is defined as the time period from the date of R0 resection to the date of disease recurrence or death. | At end of trial- up to 2 years in follow up | |
Secondary | Postoperative Complications | Postoperative complications will be recorded after each esophagectomy | within the first 3 months after esophagectomy |
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