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Demonstration of Broncholytic Effects in Subjects With Obstructive Airway Diseases by Low Frequency Ultrasound (Pabes)

F

Fraunhofer-Institute of Toxicology and Experimental Medicine

Status

Completed

Conditions

Healthy Volunteers
COPD GOLD I to IV
Asthma GINA 1 to 4

Treatments

Device: Low frequency ultrasound spectroscopy after broncholysis

Study type

Interventional

Funder types

Other

Identifiers

NCT01080924
08/10 Pabes

Details and patient eligibility

About

This study is aiming at evaluating whether low frequency ultrasound spectroscopy is a sensitive tool to detect broncholytic effects in patients with obstructive airway diseases.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • • 18 - 70 years

    • for the healthy cohort:

      • FEV1 > 80 % pred, FEV1/FVC ≥ 70 % pred., no history of allergies or asthma
      • nonsmokers, with a history of less than 1 packyear having been nonsmokers for at least the last five years
    • for the COPD cohort: COPD GOLD I to IV according to current guidelines (2)

    • for the asthma cohort: history of asthma GINA I to IV according to current guidelines (3)

    • BMI ≤ 30 kg/m2

    • Able and willing to give written informed consent

    • Available to complete all study measurements

Exclusion criteria

  • • medical conditions which prohibit the use of salbutamol

    • recent exacerbation of COPD or asthma or lower respiratory tract infection (four weeks previous to informed consent visit)
    • past or present disease, which as judged by the investigator, may affect the outcome of the study. These diseases include, but are not limited to, cardiovascular disease, malignancy, hepatic disease, renal disease, hematological disease, neurological disease, psychiatric disease, endocrine disease or pulmonary disease (including but not confined to asthma, tuberculosis, bronchiectasis or cystic fibrosis)
    • history of drug or alcohol abuse which would interfere with the subject's proper completion of the protocol assignment
    • risk of non-compliance with study procedures
    • suspected inability to understand the protocol requirements, instructions and study-related restrictions, the nature, scope, and possible consequences of the study.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Low frequency ultrasound spectroscopy
Experimental group
Description:
Low frequency ultrasound spectroscopy after broncholysis
Treatment:
Device: Low frequency ultrasound spectroscopy after broncholysis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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