Skip to content

Comparison of two different methods to inflate cuff of windpipe tube in children

Safety and efficacy of two different methods of endotracheal tube cuff inflation in children - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078423
Enrollment
104
Registered
2024-12-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Cuff inflation by manual palpation of leak method : Inflation of cuff with air by 2 cc syringe till no leak palpable in suprasternal notch in neck area while holding continuous airway

Sponsors

Institute of kidney disease and research centre Institute of Transplantation Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All children of 3-8 years of age, of either sex, ASA grade I/II posted for open urogenital surgery lasting for duration of 1-4 hrs under general anaesthesia using endotracheal intubation

Exclusion criteria

Exclusion criteria: 1.Patients with predicted difficult airway, airway abnormalities,reactive airway 2.Patients with lung disease, risk of pulmonary aspiration,requiring prolonged ventilation 3.Patients with previous sore throat, hoarseness of voice, respiratory infection in last one week,surgery requiring airway manipulation. 4.Not willing to participate 5.Patients requiring nitrous oxide as anaesthesia gas 6.Not fitting endotracheal tube size as selected by Duracher formula(age/4+3.5)

Design outcomes

Primary

MeasureTime frame
To compare percentage of intracuff pressure within recommended range (20-30 cm of H2O) in both groupsTimepoint: Initially and after supraglottic capnometry

Secondary

MeasureTime frame
To compare airway morbidity related to overinflation of cuff like sore throat (assessed at 4 and 6 hrs postoperatively) stridor, croup, laryngospasm (assessed in immediate postoperative period) in both groups.Timepoint: Immediately,4 and 6 hours after surgery

Countries

India

Contacts

Public ContactNoopur Jani

Institute of Kidney Disease and Research centre,Institute of Transplantation Sciences,Ahmedabad

noopurnaik89@gmail.com09428383183

Outcome results

None listed

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