Obstructive Airways Diseases in Emergency Department (OADED) Study

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

TERMINATED

Total Enrollment

12 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-12-22

Study Completion Date

2017-08-06

Brief Summary

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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.

Detailed Description

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This is a feasibility 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 adults asthma and COPD patients (age \>18) that arrive at the Emergency Department (ED). Patients will be enrolled on a continuous basis and will be monitored by a capnograph and an oximeter before, during and after lung function assessment and medical treatment.

Conditions

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Asthma Chronic Obstructive Pulmonary Disease (COPD)

Keywords

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Asthma COPD Capnography

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with COPD and Asthma .

Patients with COPD and Asthma. Continuous capnography and spirometry measurements of the subjects will be taken form the subjects with at least two minutes recording before the first spirometry assessment.

All clinical diagnoses and treatments will be performed according to the department's protocols.

This is an observational study with no interventions

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Age \>18
2. Ability and willingness to participate the study and sign informed consent form
3. Asthma / COPD patients

Exclusion Criteria

1. Pregnant women
2. Asthma or COPD patients with FEV1 \> 60%
3. Disability or unwillingness to undergo capnography measurement
4. Cannot be assessed for FEV1
5. Oxygen supply \>5 L/min

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ruth Stalnikowicz, Prof. ; M.D.

Role: PRINCIPAL_INVESTIGATOR

Emergency Department, Hadassah University Hospital Mount Scopus

Other Identifiers

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MDT17071

Identifier Type: -

Identifier Source: org_study_id