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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03617393
Other study ID # 2017YFC1309700
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 10, 2017
Est. completion date December 1, 2021

Study information

Verified date October 2020
Source Ruijin Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Focusing on patients with diabetes complicated with pulmonary infection, the purpose of this study is: 1) to identify the epidemiology, etiologic spectrum and status of diagnosis and treatment; 2) to develop a symptom score scale , clarify the risk factors and create a precise warning model; 3) to develop a rapid detection of pathogen of lower respiratory infection, to establish clinical pathways of early diagnosis and treatment of diabetes complicated with pulmonary infections (including bacterial, tuberculosis and fungal infections) and then make an application in clinic.


Description:

Investigators perform a observational study on 6000 patients with diabetes, among which 200 patients with pulmonary infection are included in a retrospective study and 100 patients go through metabolomics research. All patients receive clinical questionnaires, laboratory examinations and pulmonary function tests. Investigators study on pathogen distribution and infection ratio of patients above depending on follow-up survey. 1:1 nested case-control study is carried out involving 100 cases from pulmonary-infected group paired with 100 control cases matched for gender, age and fasting blood-glucose. The final purpose is to create a precise warning model in order to develop a rapid detection of pathogen of lower respiratory infection in diabetes patients. Now investigators wish to register this study to do a further research, in order to improve the early diagnosis of diabetes complicated with pulmonary infection and to reduce the mortality.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 6000
Est. completion date December 1, 2021
Est. primary completion date May 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Diagnosis by pathogen examination: positive

- Diagnosis through X-ray or CT: characteristic features of pulmonary infection

- Diagnosis through guideline of diabetes or history of diagnosed diabetes

- Age 40-70 years

Exclusion Criteria:

- Irregular follow-up and lost follow-up

- Withdraw from the study for any reason

Study Design


Locations

Country Name City State
China Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Ruijin Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival at 30 Days Accuracy and sensitivity of novel survival prediction algorithm derived from differences between the predicted and actual 30-day-survival of patients from different groups. 30 days from date of diagnosis of pulmonary infection until the date of death from any cause.
Primary Survival at 90 Days Accuracy and sensitivity of novel survival prediction algorithm derived from differences between the predicted and actual 90-day-survival of patients from different groups. 90 days from date of diagnosis of pulmonary infection until the date of death from any cause.
Primary Survival at 1 Year Accuracy and sensitivity of novel survival prediction algorithm derived from differences between the predicted and actual 1-year-survival of patients from different groups. 1 year from date of diagnosis of pulmonary infection until the date of death from any cause.
Secondary Hospitalization Time Differences in the time of hospital stay including ordinary sickroom and ICU of patients from different groups. Every 6 months from date of diagnosis of pulmonary infection until the date of death from any cause, assessed up to 3 years
Secondary Sepsis Differences in the primary and secondary sepsis after therapy according to guideline from different groups. Every 6 months from date of diagnosis of pulmonary infection until the date of death from any cause, assessed up to 3 years
Secondary CURB-65 Score Differences in confusion, urea, respiratory rate and age 65 scoring system from different groups. Every 6 months from date of diagnosis of pulmonary infection until the date of death from any cause, assessed up to 3 years
Secondary Inflammatory Parameters Differences in CRP, PCT, IL-6, IL-8, TNF-a from different groups. Day 0, day 3, day 10-14 and final result from date of diagnosis of pulmonary infection until the date of death or cure from any cause, assessed up to 1 years
Secondary Fungal Infection Examinations Assessment of G test and GM test in order to clarify the diagnosis of fungal infection. Day 0, day 3, day 10-14 and final result from date of diagnosis of pulmonary infection until the date of death or cure from any cause, assessed up to 1 years
Secondary Cryptococcal Infection Examinations Assessment latex agglutination test in order to clarify the cryptococcal infection. Day 0, day 3, day 10-14 and final result from date of diagnosis of pulmonary infection until the date of death or cure from any cause, assessed up to 1 years
Secondary Cell-mediated Immunoserologic Indexs Differences of CD3, CD4 and CD8 in different groups in order to research on cell-mediated immunity of patients with or without diabetes and pulmonary infection. Day 0, day 3, day 10-14 and final result from date of diagnosis of pulmonary infection until the date of death or cure from any cause, assessed up to 1 years
Secondary Humoral Immunoserologic Indexes Differences of IgG, IgA, IgE and IgM in different groups in order to research on cell-mediated immunity of patients with or without diabetes and pulmonary infection. Day 0, day 3, day 10-14 and final result from date of diagnosis of pulmonary infection until the date of death or cure from any cause, assessed up to 1 years
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