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Swallowing dysfunction in critically ill patients

Bronchoscopic assessment of swallowing dysfunction in critically ill patients: A prospective observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/05/052723
Enrollment
90
Registered
2023-05-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: G729- Myopathy, unspecified

Interventions

Control Intervention1: nil: nil

Sponsors

CCM department
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age > 18 years 2.48 hours to 96 hours post extubation after prolonged intubation 3.All tracheostomized patients who are already on oral feeds or in whom initiation of oral feeds is planned 4.Conscious and able to follow verbal commands [GCS at least E4 VT M6 (10T)] 5. Hemodynamically stable patients

Exclusion criteria

Exclusion criteria: 1. Presence of pre-existing dysphagia 2. Severe agitation and possible inability to cooperate with the examination 3. Bilateral obstruction of the nasal passages 4.Pre-existing neurological conditions, such as stroke and neuromuscular disease like myasthenia gravis, Lambert-Eaton myasthenic syndrome [LEMS] 5. Conditions affecting anatomic structures of the swallowing tract 6.History of recent trauma to the nasal cavity or surrounding tissue 7. Recent MI 8. Pre-existing congestive heart failure 9. Cardiac disorder with acute risk of vasovagal episode and bradycardia 10. Severe bleeding disorders and/or recent severe epistaxis (nosebleed) 11. Requiring oxygen more than 5lt/min 12.Recent trans-oesophageal echocardiography 13. Head and neck or oropharyngeal cancer

Design outcomes

Primary

MeasureTime frame
1. To identify the prevalence of swallowing dysfunction in post extubated and tracheostomised patients without pre-existing dysphagia 2. To identify the risk factors associated with the development of dysphagia 3. To correlate between the severity of dysphagia and the its effects on patient outcomes Timepoint: At the time of bronchoscopic assessment of swallowing

Secondary

MeasureTime frame
â?¢Need for reintubation, development of hospital-acquired pneumonia (HAP) â?¢Incidence of in-hospital mortality â?¢Length of ICU and hospital stay â?¢Patients discharged with feeding tube Timepoint: From the day of test to day of discharge or death

Countries

India

Contacts

Public ContactDeepika Shree

Sanjay Gandhi Post Graduate Institute Of Medical Sciences

bananip@hotmail.com8004904729

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026