Evaluation of Novel Lung Function Parameters in Patients With Interstitial Lung Disease (ILD)

NCT ID: NCT02827734

Last Updated: 2020-03-24

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

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-10-31

Study Completion Date

2020-12-31

Brief Summary

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Current diagnostic tools used in interstitial lung disease (ILD) do not meet the challenges set by the complex pathophysiology of this heterogenous group. The investigators therefore aimed to evaluate novel or not widely used diagnostic approaches for the detection and therapeutic monitoring of patients with various ILDs.

Detailed Description

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Conditions

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Pulmonary Healthy Controls Interstitial Lung Disease Idiopathic Pulmonary Fibrosis Non-specific Interstitial Pneumonia Sarcoidosis Granulomatosis With Polyangiitis (Wegener's Disease)

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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interstitial lung disease

patients with known or suspected ILD such as idiopathic pulmonary fibrosis, non-specific interstitial pneumonia, sarcoidosis, granulomatosis with polyangiitis

multiple breath washout tests

Intervention Type DEVICE

impulse oscillometry

Intervention Type DEVICE

body plethysmography

Intervention Type DEVICE

pulmonary healthy controls

patients without known or suspected pulmonary disease

multiple breath washout tests

Intervention Type DEVICE

impulse oscillometry

Intervention Type DEVICE

body plethysmography

Intervention Type DEVICE

Interventions

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multiple breath washout tests

Intervention Type DEVICE

impulse oscillometry

Intervention Type DEVICE

body plethysmography

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* known or suspected interstitial lung disease

Exclusion Criteria

* pregnancy
* inability to participate
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universitätsmedizin Mannheim

OTHER

Sponsor Role lead

Responsible Party

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Dr. Frederik Trinkmann

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Universitätsmedizin Mannheim

Mannheim, Deutschland, Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Frederik Trinkmann, Dr.

Role: CONTACT

+496213833879

Facility Contacts

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Frederik Trinkmann, Dr.

Role: primary

+496213833879

Other Identifiers

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MBW-ILD

Identifier Type: -

Identifier Source: org_study_id

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