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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04462354
Other study ID # PANGASBLUM
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date June 4, 2020
Est. completion date December 31, 2022

Study information

Verified date August 2021
Source Fundación para la Investigación del Hospital Clínico de Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A national, multicenter, randomized, prospective, parallel group clinical study to evaluate two therapeutic strategies (invaginating pancreatogastric anastomosis versus Blumgart anastomosis).


Description:

Background: Postoperative pancreatic fistula is currently the most frequent complications after duodenopancreatectomy. There are currently no RCT comparing two of the most frequently used method of pancreato-enteric anastomosis (invaginating pancreatogastric anastomosis versus Blumgart anastomosis) Hypothesis: in patients with resectable pancreatic and periampullary tumors, performing a Blumgart (AB) anastomosis for pancreatoenteric reconstruction after duodenopancreatectomy decreases the rate of postoperative pancreatic fistula (PPF) compared to to pancreatogastric anastomosis. Main goal: To comparatively evaluate the rate of PPF in patients with pancreatic and periampullary tumors undergoing cephalic duodenopancreatectomy after reconstruction with Blumgart anastomosis or pancreatogastric anastomosis.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 216
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients over 18 years old. - Diagnosis of pancreatic and periampullary tumor pathology that requires pancreatoduodenectomy - Signature of informed consent by the patient or his legal representative Exclusion Criteria: - Patients in whom liver metastases or peritoneal carcinomatosis are detected during surgery. - Patients in whom tumor resection is ultimately not achieved due to intraoperative evidence that the tumor is locally advanced, unresectable. - Patients with macroscopic residual tumor (R2). - High risk patients with severe pathology (ASA IV) according to the American Association of Anesthetists.

Study Design


Intervention

Procedure:
Blumgart Anastomosis
Patients undergoing cephalic duodenopancreatectomy, reconstructing pancreatic-enteric communication by Blumgart anastomosis
Pancreatogastric anastomosis.
Patients undergoing cephalic duodenopancreatectomy, reconstructing pancreatic-enteric communication by Pancreatogastric anastomosis.

Locations

Country Name City State
Spain Hospital Clínico Universitario de Valencia Valencia

Sponsors (2)

Lead Sponsor Collaborator
Fundación para la Investigación del Hospital Clínico de Valencia Instituto de Salud Carlos III

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative pancreatic fistula rate (PPF) The post-operative pancreatic fistula (PPF) rate will be measured using the definition of the International Study Group of Pancreatic Fistula (ISGPF) : any measurable amount of fluid from a drain placed during the operation or percutaneously, with an amylase concentration greater than three times the plasma value. 3 months
Secondary Bleeding According to the definition of the International Study Group on Pancreatic Surgery. which grades the severity of bleeding according to the clinical situation, diagnosis and need for treatment. 3 months
Secondary Gastric Emptying Delay (GED) According to the definition of the International Study Group on Pancreatic Surgery, which establishes the existence of GED when a nasogastric tube is needed for more than 3 days or is placed from the third day of the postoperative period, as well as intolerance to an oral diet at the end of the first postoperative week. 3 months
Secondary Biliary Fistula According to the definition of the International Study Group of Liver Surgery, which defines it as any measurable amount of fluid from a drain placed during the operation or percutaneously, with a concentration of bilirubin greater than three times the plasma value as of the third post-operative day. 3 months
Secondary Other complications. All complications that may occur during the first 90 days of the postoperative period (including the mortality rate) should be collected and classified according to the Clavien-Dindo classification and the Comprehensive Complication Index (CCI) 3 months
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