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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01695447
Other study ID # ZEH-LL-CX-004-02
Secondary ID
Status Recruiting
Phase N/A
First received September 20, 2012
Last updated January 25, 2017
Start date January 2012
Est. completion date December 2017

Study information

Verified date January 2017
Source Zhejiang University
Contact Xue-Li Bai, Ph.D.
Phone +86 571 87783510
Email shirleybai57@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether duct-to-mucosa is better than invagination in pancreaticojejunostomy after pancreaticoduodenectomy. This single-centre, open, randomized controlled trail is conducted following ISGPF criteria for pancreatic fistula (PF). The duration of the study is supposed to start from Jan 5th 2012 and last to Dec 2014, until 100 or more cases are accessible. Patients diagnosed with pancreatic cancer, peri-ampullar carcinoma or other benign or malignant diseases which need to operate pancreaticoduodenectomy will be included. Main outcomes are pancreatic fistula rate, mortality, morbidity, reoperation and hospital stay. The investigators assumption that duct-to-mucosa is better than invagination.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients diagnosed with pancreatic cancer or other diseases which need pancreaticoduodenectomy and pancreaticojejunostomy

- 18 to 80 y/o

- Operation-tolerated

- Informed consent

Exclusion Criteria:

- History of gastrointestinal operation

- Pancreaticoduodenectomy is given up during operation

- Pancreatic duct is difficult to locate

- Patients require to exit from the study anytime

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
duct-to-mucosa

invagination

Device:
Internal stent
Internal stent may be used during pancreaticojejunostomy according to the situation of pancreatic duct and experience of the surgeon.

Locations

Country Name City State
China the Second Affiliated Hospital, School of Medicine, Zhejiang Universtiy Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
TingBo Liang

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary pancreatic fistula The determine of pancreatic fistula follows the International Study Group on Pancreatic Fistulas (ISGPF) criteria. From date of operation until the date of dischage or date of death from any cause, whichever came first,, assessed up to 200 days
Secondary Mortality 30-day or in-hospital mortality: death from any cause within 30 days after operation or any in-hospital death are considered concerned with the type of pancreaticojejunostomy From date of operation until the date of in-hospital death or death within 30 days after operation, whichever came first, assessed up to 200 days
Secondary Morbidity any complications after operation will be recorded. From date of operation until the date of discharge or date of death from any cause, whichever came first, assessed up to 200 days
Secondary Reoperation Reasons and times of reoperation are recorded. The attending doctor will decided Whether reoperation is needed, according to indications and his experience. From date of operation until the date of discharge or date of death from any cause, whichever came first, assessed up to 200 days
Secondary Hospital stay Post-operation hospital stay is assessed. From date of operation until the date of discharge or date of death from any cause, whichever came first, assessed up to 200 days
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