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a clinical study for predicting post extubation stridor in neurosurgical patients using ultrasonographic parameters

Efficacy Of Sonographic Measurement Of Laryngeal Air Column Width And Laryngeal Air Column Difference For Predicting Post Extubation Stridor in neurosurgical patients. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/06/088563
Enrollment
257
Registered
2025-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: C729- Malignant neoplasm of central nervous system, unspecified

Interventions

None listed

Sponsors

academic division
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients admitted and undergoing neurosurgical procedures at Sree Chitra Tirunal Institute for Medical Sciences and Technology

Exclusion criteria

Exclusion criteria: 1.Patient refusal or refusal by patient bystanders 2. Patients with a history of any airway related surgeries 3.Patient with history of previous tracheostomy 4. Patients that will undergo elective tracheostomy 5. Patients undergoing emergency surgeries 6. Pregnant and lactating mothers

Design outcomes

Primary

MeasureTime frame
StridorTimepoint: Within 1st 24 hour of postoperative period—

Secondary

MeasureTime frame
TO FIND OUT THE RISK FACTORS FOR POSTEXTUBATION STRIDOR IN NEUROSURGICAL CASESTimepoint: 24HOURS POST EXTUBATION—

Countries

India

Contacts

Public ContactDr Smita V

SREECHITHRA THIRUNAL INSTITUTE OF MEDICAL SCIENCES AND TECHNOLOGY

hsp666@gmail.com09447773095

Outcome results

None listed

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