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Completed

NCT Number: NCT02805114

Obstructive Airways Diseases in Pulmonary Clinic (OADPC) Study

This is an observational study which aims to evaluate the possibility of using data from a capnography device to assess obstructive airway severity in both Chronic Obstructive Pulmonary Disease (COPD) and Asthma patients.

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Key information

Conditions

Asthma Bronchial Diseases Chronic Disease Chronic Obstructive Pulmonary Disease (COPD) Disease Attributes Hypersensitivity Hypersensitivity, Immediate Immune System Diseases Lung Diseases Lung Diseases, Obstructive Pathologic Processes Pathological Conditions, Signs and Symptoms Pulmonary Disease, Chronic Obstructive Respiratory Hypersensitivity Respiratory Tract Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Pulmonary Institute Rabin Medical center, Beilinson Hospital

Petah Tikva, 49100, Israel

About this study

This is an observational study which aims to evaluate the possibility of using data from a capnography device to assess obstructive airway severity in both COPD and Asthma patients. The study will include adult asthma and COPD patients (age >18). Patients will be enrolled on a continuous basis and will be monitored by capnograph and oximeter before and after lung function assessment and also during and after medical treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18
  • Ability and willingness to participate the study and sign informed consent form
  • Asthma / COPD patients

Exclusion criteria

  • Pregnant women
  • Asthma or COPD patients with FEV1 > 80%
  • Disability or unwillingness to undergo capnography measurement
  • Cannot be assessed for FEV1
  • Oxygen supply >5 L/min
  • 6. Subjects that gone through LOBECTOMY OF LUNG in the last 5 years.

Treatment and study plan

Primary outcomes

  1. Correlation between capnography parameters and severity of asthma

    Time frame: 1/2 hour to 48 hours from enrollment of subjects

    Correlation between the airway obstruction severity calculation based on the capnography parameters and the clinical severity of asthma and COPD as defined by forced expiratory volume in 1 second (FEV1), in severe asthma and COPD patients

Sponsors and collaborators

Lead sponsor

Oridion

Industry

Collaborators

  • Rabin Medical Center

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Jun 17, 2016
Registry last updated
Jan 10, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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