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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03711435
Other study ID # XZTCM2018LSY-013
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 20, 2018
Est. completion date February 5, 2020

Study information

Verified date July 2022
Source Xuzhou Traditional Chinese Medicine Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The pathogenesis of idiopathic pulmonary interstitial fibrosis is complex, and there is no specific biomarkers, the treatment effect is not such useful. Currently, it is discovered that Chinese medicine treatment may be effective. The investigators select patients with idiopathic pulmonary interstitial fibrosis and healthy controls, use metabolomics to study the biological characteristics of idiopathic pulmonary interstitial fibrosis, screen biomarkers of IPF, and label different TCM syndromes of IPF, explore the biological nature of IPF TCM syndromes, find the biological changes that occur during the development and progression of IPF and explore the metabolite marker clusters of IPF. Furthermore, the results of this study may find its diagnostic significance for IPF and Looking for potential targets for future treatment of IPF.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date February 5, 2020
Est. primary completion date February 5, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 85 Years
Eligibility Inclusion Criteria: - Case group inclusion criteria 1. According to the diagnostic criteria published in 2015, the New Guidelines for the Diagnosis and Treatment of Idiopathic Pulmonary Fibrosis, jointly developed by the American Thoracic Society, the European Respiratory Society, the Japanese Respiratory Society, and the Latin American Thoracic Society; 2. aged 50 to 85 years old; Control group inclusion criteria: Health people match on the age (±3 years old) and gender with case group with 1:1 rate at the same time. Exclusion Criteria: - Case group exclusion criteria: 1. Those with severe heart, liver, kidney and other organ dysfunction or suffering from blood diseases; 2. with malignant tumors; 3. Severely infected people; 4. Pregnant and lactating women; 5. mental illness, serious obstacles and those who are unwilling to cooperate; Control group exclusion criteria: 1. Those with severe heart, liver, kidney and other organ dysfunction or blood disease; 2. With malignant tumors; 3. Chest X-ray or chest low-dose CT suggesting intra-pulmonary interstitial fibrosis; 4. With chronic pulmonary diseases such as pulmonary interstitial disease, chronic obstructive pulmonary disease, and bronchial asthma; 5. With connective tissue disease and those with a history of exposure to occupational diseases; 6. Mental illness, serious obstacles and unwilling to cooperate.

Study Design


Locations

Country Name City State
China Xuzhou Traditional Chinese Medicine Hospital Xuzhou Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Xuzhou Traditional Chinese Medicine Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary biomarkers detected in metabolites Metabolomics of serum based on mass spectrometry.It is non-targeted metabolomics.The study is to find the target metabolite to distinguish IPF. 1 year
Secondary High-resolution chest CT total score (CT-Tot) High-resolution chest CT total score (CT-Tot), which includes the grid shadow and the honeycomb lung. The score range is 0-5, and the larger the score, the more serious the disease. 1 year
Secondary Six Minute Walk Test(6MWT) The six-minute walk test measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface.It is a simple objective indicator for evaluating cardiopulmonary function 1 year
Secondary Pulmonary function Pulmonary function Pulmonary function including forced vital capacity(FVC),forced expiratory volume at one second(FEV1),diffusion capacity of lung for carbon monoxide(DLCO) 1 year
Secondary St. George's Respiratory Questionnaire St. George's Respiratory Questionnaire is measuring impaired health and perceived well-being ('quality of life') in airways disease. the score is 0 to 100,the higher the score is,the worse life quality the patients has. 1 year
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