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Clinical Trials/CTRI/2025/08/092180
CTRI/2025/08/092180Not yet recruitingNot Applicable

To study correlation of spirometry and forced oscillometry in patients of chronic obstructive airway disease- retrospective observational study

DRHEYMA KRISHNA MANOHARAN1 site in 1 country90 target enrollmentStarted: August 30, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
90
Locations
1
Primary Endpoint
1 To study the correlation of FEVI obtained by spirometry with R5, R5-R20, Ax, X5, Fres obtained by forced Oscillometry.

Study Overview

Brief Summary

I.          Pulmonary department at AIIMS Rajkot started performing spirometry from March 2022. Forced oscillometry from November 2023. So list of all patients who were diagnosed with COPD from November 2023 till date will be retreived from the electronic medical record of the department.

II.          Patient of COPD who have undergone spirometry and forced oscillometry will be selected for inclusion in the study after obtaining written informed consent.

III.          Data extracted will include:

1.Demographic data- Age, Gender, occupation, residence.

2.Smoking status- Bidi/cigarette, smoking index, packs in year.

3.COPD GOLD stage.

  1. Aetiology of COPD.

5.Spirometry parameters FEV1, FVC. FEV1/FVC, FEF 25-75 pre and post bronchodilator.

  1. Forced oscillometry parameters – R5, R5-R20, Ax, Pre and Post Bronchodilator.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
45.00 Year(s) to 80.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patient of COPD who have undergone spirometry and forced oscillometry will be selected for inclusion in the study after obtaining written informed consent.

Exclusion Criteria

  • Those patient who do not give consent.

Outcomes

Primary Outcomes

1 To study the correlation of FEVI obtained by spirometry with R5, R5-R20, Ax, X5, Fres obtained by forced Oscillometry.

Time Frame: 1 To study the correlation of FEVI obtained by spirometry with R5, R5-R20, Ax, X5, Fres obtained by forced Oscillometry. | 2.To study the correlation of FEF25-75 obtained by spirometry with R5, R5-R20, Ax, Fres, X5 obtained by forced oscillometry. | 3.To study the correlation of postbronchodilator change in FEV1 with R5 and R5-R20.

2.To study the correlation of FEF25-75 obtained by spirometry with R5, R5-R20, Ax, Fres, X5 obtained by forced oscillometry.

Time Frame: 1 To study the correlation of FEVI obtained by spirometry with R5, R5-R20, Ax, X5, Fres obtained by forced Oscillometry. | 2.To study the correlation of FEF25-75 obtained by spirometry with R5, R5-R20, Ax, Fres, X5 obtained by forced oscillometry. | 3.To study the correlation of postbronchodilator change in FEV1 with R5 and R5-R20.

3.To study the correlation of postbronchodilator change in FEV1 with R5 and R5-R20.

Time Frame: 1 To study the correlation of FEVI obtained by spirometry with R5, R5-R20, Ax, X5, Fres obtained by forced Oscillometry. | 2.To study the correlation of FEF25-75 obtained by spirometry with R5, R5-R20, Ax, Fres, X5 obtained by forced oscillometry. | 3.To study the correlation of postbronchodilator change in FEV1 with R5 and R5-R20.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
DRHEYMA KRISHNA MANOHARAN
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Heyma krishna Manoharan

Senior resident

Study Sites (1)

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