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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02965300
Other study ID # S2016-110-01
Secondary ID
Status Recruiting
Phase N/A
First received November 14, 2016
Last updated November 14, 2016
Start date October 2016
Est. completion date August 2017

Study information

Verified date November 2016
Source Chinese PLA General Hospital
Contact Liang—an Chen, MD,PHD
Phone 8610-55499027
Email cla301@126.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The purpose of this study is to analysis the volatile organic gases(VOCs) in exhaled breath of pulmonary lesion patients and healthy controls, in order to find the difference of composition and concentration among groups.


Description:

Collect the exhaled gas in pulmonary lesion patients and healthy controls, using proton transfer reaction mass spectrometry to analysis the different composition and concentration of VOCs, to find the biomarker gases of distinguishing benign and malignant lesion of lung among different groups, and try to build a diagnostic model for lung lesion.


Recruitment information / eligibility

Status Recruiting
Enrollment 230
Est. completion date August 2017
Est. primary completion date May 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- cohort 1 :

Inclusion criteria:

Patients newly diagnosed with primary lung cancer by tissue biopsy and did not receive any treatment aiming at the tumor, including chemotherapy and radiotherapy.

Age = 18 years

- cohort 2: Inclusion criteria: Patients diagnosed with pulmonary benign lesion by tissue biopsy or other examination.

Age = 18 years

Exclusion Criteria:

patients who have more than one type of carcinoma patients diagnosed type 2 diabetes mellitus patients diagnosed chronic renal failure patients diagnosed upper digestive tract ulcer patients who reject to sign the informed consent from

- cohort 3: Healthy controls Volunteers without diagnosed lung diseases and pulmonary symptoms.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China department of respiratory department ,Chinese PLA general hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Chinese PLA General Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mass-to-charge Ratio It is the measurement result of VOCs in exhaled breath using PTR-MS device. 6 months No
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