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Coughing in Infratentorial Brain Lesion Patients

Cross Sectional Observation Study of Cough Dysfunction in Infratentorial Brain Lesion Patients, as Assessed by M-mode Sonography

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02081040
Enrollment
42
Registered
2014-03-07
Start date
2013-09-30
Completion date
2014-08-31
Last updated
2015-02-24

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

Conditions

Stroke

Keywords

brainstem, diaphragm, deglutition disorder, sonography

Brief summary

To record diaphragm excursion in infratentorial brain lesions patients with dysphagia during coughing and compare them to those with supratentorial brain lesion patients with dysphasia and those with no dysphagia at a university affiliated rehabilitation department.

Detailed description

Our previous work has shown that stroke patients with dysphagia have impaired diaphragm excursion in comparison to those with no dysphagia. It has been postulated that respiratory and cough function are primarily controlled by respiratory and swallowing centers located in the brainstem.We postulated that those with infratentorial brain lesions would have more impaired cough and respiratory function than those with non-brainstem lesions and supratentorial brain lesions. However there has been no studies whether those with infratentorial brain lesions have more impaired cough function and decreased diaphragm excursion than those with supratentorial brain lesions.

Interventions

OTHERNot applicable (observational study with no active intervention)

Sponsors

The Catholic University of Korea
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Group 1- Brainstem lesion subjects with dysphagia that would require insertion of a nasogastric tube Group 2- Non-brainstem lesion subjects with dysphagia that would require insertion of a nasogastric tube Group 3- Stroke patients with no evidence of dysphagia

Exclusion criteria

* Episode of acute pneumonia or pulmonary embolism at time of enrollment * Previous history of chronic respiratory disorders or other systemic disorders that may affect respiratory function ( ex, rheumatoid arthritis, chronic renal disease, spinal cord injury) * Stroke patients with multiple brain lesions * Episode of Diaphragm weakness due to peripheral polyneuropathy or unilateral phrenic nerve palsy * Previous episode of abdominal or thoracic surgery within one year of enrollment * Concomitant diagnosis of myopathy, muscular dystrophy or other disorders that may affect respiratory muscles. * Episode of rib fracture within one year of enrollment * Chronic alcoholism * Patient with previous diagnosis of dementia or with impaired cognitive function that may limit full participation at the evaluation * Patient with tracheostomy state

Design outcomes

Primary

MeasureTime frameDescription
Diaphragm excursionbaseline one timeDiaphragm excursion as assessed by m mode sonography

Secondary

MeasureTime frame
Maximal inspiratory pressurebaseline one time
Peak cough flow force during voluntary coughingbaseline one time

Other

MeasureTime frameDescription
maximal expiratory pressurebaseline one time
spirometry findingsbaseline one time
Cough force during reflexive coughingbaseline one timePeak flow force during reflexive coughing

Countries

South Korea

Outcome results

None listed

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