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Clinical Trial of Quantitative Detection Kit for Hsp90α in Hepatic Cancer

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ClinicalTrials.gov Identifier: NCT02324127
Recruitment Status : Unknown
Verified December 2014 by Protgen Ltd.
Recruitment status was:  Active, not recruiting
First Posted : December 24, 2014
Last Update Posted : December 24, 2014
Sponsor:
Information provided by (Responsible Party):
Protgen Ltd

Study Description
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Brief Summary:
Detect plasma Hsp90α concentration of liver cancer patients, healthy volunteers, benign liver diseases.

Condition or disease Intervention/treatment Phase
Liver Cancer Device: hsp90 Not Applicable

Detailed Description:
Detect plasma Hsp90α concentration of liver cancer patients, healthy volunteers, benign liver diseases, validate accuracy, specificity and sensitivity of Hsp90α kit.
Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 1100 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Clinical Trial of Quantitative Detection Kit for Hsp90α in Hepatic Cancer
Study Start Date : October 2012
Estimated Primary Completion Date : December 2014
Estimated Study Completion Date : December 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Liver Cancer

Arms and Interventions
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Arm Intervention/treatment
Experimental: liver cancer
Detect plasma Hsp90α concentration of liver cancer patients
 Device: hsp90
Detect plasma Hsp90α concentration of lung cancer patients
Other Name: biomarker


Outcome Measures
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Primary Outcome Measures :
  1. Hsp90α Concentration of plasma [ Time Frame: 4 months ]
    Detect Hsp90α Concentration(ng/ml) of plasma and calculate the accuracy, specificity and sensitivity of Hsp90α kit


Eligibility Criteria
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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Liver cancer patients
  • Healthy volunteers,
  • Benign liver diseases patients

Exclusion Criteria:

  • Patients who Previously accepted radiotherapy
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02324127


Locations
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China, Zhejiang
Zhejiang Medical University Cancer Institute and Hospital
Hangzhou, Zhejiang, China
Sponsors and Collaborators
Protgen Ltd
Investigators
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Principal Investigator: Shusen Zhen, MD The first hospital of Zhejiang province
More Information
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Responsible Party: Protgen Ltd
ClinicalTrials.gov Identifier: NCT02324127    
Other Study ID Numbers: hsp90a2011-05
First Posted: December 24, 2014    Key Record Dates
Last Update Posted: December 24, 2014
Last Verified: December 2014
Additional relevant MeSH terms:
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Liver Neoplasms
Digestive System Neoplasms
Neoplasms by Site
 Neoplasms
Digestive System Diseases
Liver Diseases