- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02324114
Clinical Trial of Quantitative Detection Kit for Hsp90α in Colorectal Cancer
December 22, 2014 updated by: Protgen Ltd
Detect plasma Hsp90α concentration of colorectal cancer patients, healthy volunteers, benign colorectal diseases patients.
Study Overview
Detailed Description
Detect plasma Hsp90α concentration of colorectal cancer patients, healthy volunteers, benign colorectal diseases patients, validate accuracy, specificity and sensitivity of Hsp90α kit.
Study Type
Interventional
Enrollment (Anticipated)
1100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xianrang Song, MD
- Phone Number: 87984777 0531
Study Contact Backup
- Name: Lisheng Liu, MD
- Phone Number: 87984777 0531
- Email: wufei@protgen.com
Study Locations
-
-
Shandong
-
Jinan, Shandong, China
- Recruiting
- Shandong province cancer hospital
-
Contact:
- Lisheng Liu, MD
- Phone Number: 87984777 0531
- Email: wufei@protgen.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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- colorectal cancer patients, healthy volunteers, benign colorectal diseases patients
Exclusion Criteria:
- Patients who previously accepted radiotherapy
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Rectal cancer
Detect plasma Hsp90α concentration of patients,
|
Detect plasma Hsp90α concentration
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hsp90α Concentration(ng/ml) of plasma
Time Frame: 4 months
|
Detect Hsp90α Concentration(ng/ml) of plasma and calculate the accuracy, specificity and sensitivity of Hsp90α kit
|
4 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jinming Yu, MD, Shandong province cancer hospital
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
September 1, 2012
Primary Completion (Anticipated)
December 1, 2014
Study Completion (Anticipated)
December 1, 2014
Study Registration Dates
First Submitted
December 14, 2014
First Submitted That Met QC Criteria
December 22, 2014
First Posted (Estimate)
December 24, 2014
Study Record Updates
Last Update Posted (Estimate)
December 24, 2014
Last Update Submitted That Met QC Criteria
December 22, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- hsp90a2011-03
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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