2015-06
2016-10
2016-12
45
NCT02451384
Shanghai Zhongshan Hospital
Shanghai Zhongshan Hospital
INTERVENTIONAL
According CTC to Compare the Influences of Different Methods to Remove the PDAC
Acccording circulating tumor cells to compare the differences of different methods(routine method、no-touch principle method、laparoscopy method) to remove the ductal adenocarcinoma of pancreatic body and tail.
N/A
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates | Results Reporting Dates | Study Record Updates |
---|---|---|
2015-05-14 | N/A | 2015-06-28 |
2015-05-21 | N/A | 2015-06-30 |
2015-05-22 | N/A | 2015-06 |
This section provides details of the study plan, including how the study is designed and what the study is measuring.
Primary Purpose:
Treatment
Allocation:
Randomized
Interventional Model:
Parallel
Masking:
None
Arms and Interventions
Participant Group/Arm | Intervention/Treatment |
---|---|
EXPERIMENTAL: routine surgery In this arm the patients will be performed routine surgery to remove the tumors. And then we compare their circulating tumor cell countings in the pre and post-operation. | PROCEDURE: routine surgery
|
EXPERIMENTAL: no-touch surgery In this arm the patients will be performed no-touch surgery to remove the tumors. And then we compare their circulating tumor cells countings in the pre and post-operation. | PROCEDURE: no-touch surgery |
EXPERIMENTAL: laparoscopy surgery In this arm the patients will be performed laparoscopy surgery to remove the tumors. And then we compare their circulating tumor cells countings in the pre and post-operation. | PROCEDURE: laparoscopic surgery |
Primary Outcome Measures | Measure Description | Time Frame |
---|---|---|
the changes of CTCs countings between the pre and post-operation in each arm | Within 1 week after the surgeries are completed in any arm | |
the changes of CTCs countings between the pre and post-operation among the arms | Within 2 weeks after the surgeies are all completed |
Secondary Outcome Measures | Measure Description | Time Frame |
---|
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.
Ages Eligible for Study:
ALL
Sexes Eligible for Study:
18 Years
Accepts Healthy Volunteers:
This is where you will find people and organizations involved with this study.
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
No publications available