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Evaluation of Diaphragm in Chronic Obstructive Pulmonary Disease Patients by Ultrasound in Relation to Severity

Evaluation of Diaphragm in Chronic Obstructive Pulmonary Disease Patients Using Ultrasonography in Relation to Disease Severity in Fayoum University Hospital

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05035875
Enrollment
80
Registered
2021-09-05
Start date
2019-12-14
Completion date
2020-12-14
Last updated
2021-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

ultrasonography, diaphragm, COPD, Fayoum

Brief summary

The study of the diaphragm is an important point in the assessment of COPD patients. Ultrasonographic evaluation of the diaphragm is considered a simple, non-invasive, available bedside technique. Ultrasonography can be used for evaluation of the site, structure, and motion of the diaphragm, assessment of excursion, and thickness. The aim of the study is ultrasonographic assessment of the diaphragm in COPD patients and its relation to disease severity

Detailed description

The study was conducted on eighty patients, forty COPD patients who were diagnosed and classified into four groups according as following: The first group: included 10 patients with a mild stage. The second group: included 10 patients with a moderate stage. The third group: included 10 patients with a severe stage. The fourth group: included 10 patients with a very severe stage. The study also included forty healthy individuals of the same age and sex as COPD patients. All participants gave their informed consent for inclusion before sharing in the study. Every person was submitted to: Full medical history, Clinical examination,Chest x-ray, spirometry and ultrasonographic assessment of diaphragm function (thickness and excursion)

Interventions

DEVICEultrasonography

ultrasound assessment of diaphragm function

Sponsors

Enas Sayed Farhat
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
MALE
Age
40 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* • Stable COPD patients aged more than 40 years who were diagnosed and classified into four groups of severity according to GOLD 2020. * Age and sex-matched healthy controls

Exclusion criteria

* • Patient with a known neuromuscular disorder. * Patient with known anatomical malformation of the diaphragm. * Post abdominal or thoracic surgery.

Design outcomes

Primary

MeasureTime frameDescription
measure diaphragmatic thickness by ultrasound1 year studymeasure diaphragmatic thickness at total lung capacity and residual volume in millimetres to calculate diaphragm thickness fraction
measure diaphragm excursion by ultrasound1 year studymeasure diaphragm excursion in centimetres at zone of apposition

Secondary

MeasureTime frameDescription
spirometry assessment1 year studyvalue of forced expiratory volume in first second is assessed as a percentage of normal by spirometry to assess disease severity
questionnaires1 year study( modified medical research council and chronic obstructive pulmonary disease assessment test) to detect severity of the disease

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026