- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02633436
Research on the Role of SLC1A5 in the Development of Esophageal Cancer
Research on the Role of the Amino Acid Transporter SLC1A5 in the Development of Esophageal Cancer
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This will be an observational study. The investigators will aim to enroll 100 male and female adult patients (aged 18 years and over) of all ethnicities/races, who have been referred to the Fourth Affiliated Hospital of Guangxi Medical University for esophageal cancer.
The investigators will be using a standardized data collection form. This is an observational study in which standard of care will be practiced and the patients are not placed at additional risk from participating in this study. However, as the investigators are collecting data prospectively, all participants will sign consent. An attempt will be made to see if there is a correlation between the expression of SLC1A5 with esophageal cancer.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Zheng Peng
- Phone Number: +86 18589966550
- Email: labstar@qq.com
Study Contact Backup
- Name: Shengming Dai, Dr.
- Phone Number: +86 13978026884
- Email: daishm@sina.com
Study Locations
-
-
Guangxi
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Liuzhou, Guangxi, China, 545000
- Recruiting
- The Fourth Affiliated Hospital of Guangxi Medical University
-
Contact:
- Zheng Peng
- Phone Number: +86 18589966550
- Email: labstar@qq.com
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Liuzhou, Guangxi, China, 545000
- Recruiting
- Liuzhou Maternity and Child Healthcare Hospital
-
Contact:
- Xiaolan Lv
- Phone Number: +86 15577727711
- Email: 13505525@qq.com
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with histologically proven esophageal cancer;
- Age ≥18 years;
- All patients must sign consent forms voluntarily;
Exclusion Criteria:
- Inability to obtain histologic proof of malignancy.
- Age <18 years;
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
cancer tissues
SLC1A5 expression of esophageal cancer tissues from patients
|
To observe the expression of SLC1A5 by immunohistochemistry and WesternBlot analysis.
|
paired adjacent tissues
SLC1A5 expression of paired adjacent esophageal tissues from patients
|
To observe the expression of SLC1A5 by immunohistochemistry and WesternBlot analysis.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
optical density (ODs) of each slice by immunohistochemistry assay
Time Frame: within one year (plus or minus 1 month) after surgery
|
For immunohistochemistry assay: Briefly, the samples will be cut into slices, which will be stained with standard steps.
Finally, three high power fields will be randomly selected from each slice and the average optical density (OD) will be measured in each field.
|
within one year (plus or minus 1 month) after surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
SLC1A5 expression detected by WesternBlot
Time Frame: within one year (plus or minus 1 month) after surgery
|
Western blot assay will be done by comparing the intensity of bands.
To start with, xray film will be scanned on a flat-bed scanner.
Then the grayscale image will be analyzed with software.
Finally the Gray Value of each band will be obtained for analysis.
|
within one year (plus or minus 1 month) after surgery
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Xiangcheng Wei, Guangxi Medical University Institutional Review Board
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PJK201518
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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