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AIRWAY TUBE PRESSURE CUFF ASSESSING â?? TO COMPARE PATIENTS BETWEEN MANUAL AND AUTOMATIC MANOMETER IN SURGERIES UPTO 3 HOURS

ENDOTRACHEAL TUBE CUFF PRESSURE MONITORING â?? COMPARISON OF SAFETY PROFILE BETWEEN MANUAL AND AUTOMATIC MANOMETER. IN SURGERIES LASTING FOR UPTO 3 HOURS.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035794
Enrollment
72
Registered
2021-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: MANOMETER: Endotracheal Cuff pressure monitoring device, Duration of intervention is upto 3hrs. Control Intervention1: Manual: Manual method to monitor Endotracheal cuff pressure

Sponsors

Shri BM Patil Medical College Hospital and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex or age between 20 to 50 years. Patients with ASA grade 1 and 2,Malampatti grade 1 and 2 Surgeries posted under general anesthesia lasting for up to 3 hours High volume,low-pressure cuff,single use,oral Portex tube with an internal diameter of 7.0-8.5mm

Exclusion criteria

Exclusion criteria: All emergency intubations,pregnant patients, trauma cases involving anterior cervical spine injuries excluded. Patients with hepatic or renal insufficiency Patients with neurologic and psychiatric disease Patient refusal Patient having bleeding disorders Patients with H/o Cardio-Respiratory disorders

Design outcomes

Primary

MeasureTime frame
To compare and evaluate the intraoperative parameters such as pulse and blood pressure as a result of changes occurring in the endotracheal tube cuff pressure.Timepoint: 3 hours

Secondary

MeasureTime frame
To compare the incidence of post-operative complications using the two methods of maintenance of endotracheal tube cuff pressure, like hoarseness, sore throat, inspiratory stridor, dyspnea, aspiration pneumonitis and complete obstruction.Timepoint: 24 hours

Countries

India

Contacts

Public ContactDIVYA M

SHRI B.M.PATIL MEDICAL COLLEGE HOSPITAL

vidyapatila@gmail.com9448131260

Outcome results

None listed

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