- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03515850
Anatomical Classifications of Inferior Mesenteric Artery (IMA)
April 23, 2018 updated by: Li Chuan
Clinical Trial of Anatomical Classifications of Inferior Mesenteric Artery in Laparoscopic Rectal Resection Surgery
The vascular branches of inferior mesenteric artery (IMA) involve superior rectal artery(SRA),Sigmoid artery(SA) and the left colic artery(LCA).
Different levels of ligation of the (IMA) are applied in rectal cancer surgery, including retain or not retain the left colic artery(LCA).
Retained the LCA would facilitate the vascularity.
The variations of vessels are more frequent in the combinations of branches, while LCA, SA and SRA may vary from people to people.
Which contribute to the difficulty of surgery to retain the LCA..
As a result, a better understanding of the anatomical branches classification of IMA is a must during operation.
However, existing studies of IMA's branches combination are very rare and often single-centered with minimal samples.
In order to achieve better surgical outcome and reduce operative complications, the investigators design this study to investigate the anatomical classification of IMA and the surgical outcome of each type
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Chongqing, China, 400038
- Recruiting
- General Surgery Center of PLA
-
Contact:
- Yu Peiwu, M.D/Ph.D
- Phone Number: +862368754167
- Email: yupeiwu01@sina.com
-
-
Participation Criteria
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.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
This study is a prospective study,and based on the conjoin classifications of branches, the anticipant populations of this study is 500.
Description
Inclusion Criteria:
- Patients who undergoing laparoscopic rectal cancer surgery.
- Pathology: adenocarcinoma or huge adenomas proven by colonoscopic biopsy.
- Localization: tumor located between distal sigmoid colon and anal canal.
- Patients have to be aware of the aim of the trial, and have signed the informed consent.
Exclusion Criteria:
- History of any gastrointestinal surgery.
- Patients with emergent surgery.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
classifications vascular branches of IMA
Time Frame: 3years
|
based on the positon of LCA that conjoin the IMA
|
3years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
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 Major Dates
Study Start (Actual)
January 5, 2018
Primary Completion (Anticipated)
July 1, 2019
Study Completion (Anticipated)
January 30, 2021
Study Registration Dates
First Submitted
April 23, 2018
First Submitted That Met QC Criteria
April 23, 2018
First Posted (Actual)
May 4, 2018
Study Record Updates
Last Update Posted (Actual)
May 4, 2018
Last Update Submitted That Met QC Criteria
April 23, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Southwest-IMA-rectal
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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