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Clinical Trial of Quantitative Detection Kit for Hsp90α in Hepatic Cancer

NCT ID: NCT02324127

Last Updated: 2014-12-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

1100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-10-31

Study Completion Date

2014-12-31

Brief Summary

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Detect plasma Hsp90α concentration of liver cancer patients, healthy volunteers, benign liver diseases.

Detailed Description

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Detect plasma Hsp90α concentration of liver cancer patients, healthy volunteers, benign liver diseases, validate accuracy, specificity and sensitivity of Hsp90α kit.

Conditions

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Liver Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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liver cancer

Detect plasma Hsp90α concentration of liver cancer patients

Group Type EXPERIMENTAL

hsp90

Intervention Type DEVICE

Detect plasma Hsp90α concentration of lung cancer patients

Interventions

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hsp90

Detect plasma Hsp90α concentration of lung cancer patients

Intervention Type DEVICE

Other Intervention Names

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biomarker

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* Patients who Previously accepted radiotherapy
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Protgen Ltd

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Shusen Zhen, MD

Role: PRINCIPAL_INVESTIGATOR

The first hospital of Zhejiang province

Locations

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Zhejiang Medical University Cancer Institute and Hospital

Hangzhou, Zhejiang, China

Site Status

Countries

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China

Other Identifiers

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hsp90a2011-05

Identifier Type: -

Identifier Source: org_study_id