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The Effect of Monitoring Endotracheal Tube Cuff Pressure and Keeping it in a Certain Range

NCT06353932 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 263

Last updated 2024-04-09

No results posted yet for this study

Summary

The main purpose of our prospective, randomized, controlled, double-blind study is to investigate the effect of keeping endotracheal tube cuff pressures within a certain range on the incidence of postoperative sore throat, hoarseness and cough.The secondary aims of our study are to evaluate the effect of intubation duration, smoking, presence of chest disease, presence of blood on the intubation tube after extubation, presence of NG\\OG, and type of surgery on the incidence of sore throat, hoarseness, and cough.The patients were randomly divided into two: a study group with continuous cuff pressure monitoring and a control group without continuous cuff pressure monitoring.The endotracheal cuff pressure of the patients in both groups was measured by a blinded researcher using a cuff manometer after intubation, before extubation, and in long cases, at the 3rd hour after intubation.Patients were evaluated for sore throat, cough, and hoarseness at the 2nd and 24th hours by another researcher blinded to the study groups.

Conditions

  • Endotracheal Tube
  • Cuff Pressure
  • Sore Throat

Interventions

OTHER

keeping the endotracheal tube cuff pressure within a certain range

The endotracheal tube cuff pressures of the study group patients were kept within the range of 20-25 cm H2O.

Sponsors & Collaborators

  • Hacettepe University

    lead OTHER

Principal Investigators

  • Murat İzgi, Ass. Prof. · Hacettepe University Department of Anesthesiology

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-25
Primary Completion
2024-02-25
Completion
2024-02-25

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06353932 on ClinicalTrials.gov