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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04078412
Other study ID # 4-2017-0958
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date November 21, 2017
Est. completion date November 2027

Study information

Verified date November 2019
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background:

NTM(Nontuberculous mycobacteria) pulmonary disease is increasing worldwidely, however the diagnosis and treatment of NTM pulmonary disease still has multiple obstacles. The initiation of treatment is not necessary for all patients with NTM pulmonary disease. In addition, the drugs for treatment of NTM pulmonary disease is not enough.

objective. The aim of this prospective registry for Nontuberculous mycobacterial pulmonary disease is to register the NTM pulmonary patients and analysis of the treatment outcome based on the species and to collect the blood and urine samples from the patients for exploring the biomarker for diagnosis and monitoring the NTM pulmonary disease and collect the nontuberculous mycobacterium.

Methods:

1. informed consents

2. register in cohort and collect the clinical information and serum, plasma, urine and mycobacteria

3. follow up 6 months to 1year based on the clinical situation

Analysis:

1. treatment outcome based on NTM-NET consensus statement

2. exploration of biomarker for progression and monitoring of treatment response


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 114
Est. completion date November 2027
Est. primary completion date November 2027
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

1. age 20 or more than 20 years

2. diagnosed by ATS criteria for NTM pulmonary disease

Exclusion Criteria:

1) not specific

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Department of Internal Medicine, Yonsei University College of Medicine Division of Pulmonology, Severance Hospital, Yonsei University Health System Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary treatment outcome based on NTM-NET consensus statement For patients who need the treatment for NTM pulmonary disease : treatment outcome based on the NTM -NET consensus : microbiologic results, clinical symptoms and radiologic results
For patients who don't need the treatment for NTM pulmonary disease : progression of NTM-PD defined by clinical, microbiotic and radiologic results.
At the end of the treatment or 12months after treatment
Secondary biomarker for disease progression: RNA sequence analysis exploration for various biomarkers with RNA sequence analysis at the beginning of the treatment
Secondary biomarker for disease progression: metabolomic analysis exploration for various biomarkers with metabolomic analysis at the beginning of the treatment
Secondary biomarker for disease progression: RNA sequence analysis exploration for various biomarkers with RNA sequence analysis at the end of the treatment (through study completion, an average of 12 to 15month after treatment)
Secondary biomarker for disease progression: metabolomic analysis exploration for various biomarkers with metabolomic analysis at the end of the treatment (through study completion, an average of 12 to 15month after treatment)
Secondary biomarker for monitoring of treatment response: RNA sequence analysis exploration for various biomarkers with RNA sequence analysis at the beginning of the treatment
Secondary biomarker for monitoring of treatment response: metabolomic analysis exploration for various biomarkers with metabolomic analysis at the beginning of the treatment
Secondary biomarker for monitoring of treatment response: RNA sequence analysis exploration for various biomarkers with RNA sequence analysis at the end of the treatment (through study completion, an average of 12 to 15month after treatment)
Secondary biomarker for monitoring of treatment response: metabolomic analysis exploration for various biomarkers with metabolomic analysis at the end of the treatment (through study completion, an average of 12 to 15month after treatment)