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Study identifier: NCT06537362 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Mouthpiece With Integrated Cheek Support vs. Manual Cheek Support During Respiratory Oscillometry

Condition: Respiratory Morbidity · Lung Function Decreased  ·  Sponsor: Politecnico di Milano

PhaseNA
Planned participants55
Who can joinAll sexes, 5 Years to 75 Years
Healthy volunteersYes

About this study

The study aims to evaluate the measurement accuracy of respiratory impedance during oscillometry (or Forced Oscillation Technique - FOT) under the following conditions: 1)The subject's cheeks are manually supported by an expert (Gold Standard method), 2) The subject's cheeks are supported by an integrated cheek support in the mouthpiece. It is a prospective, randomized, cross-over study on Subjects who will present themselves at the offices of the participating doctors, aged between 5 and 75 years. The primary outcome is to Compare the respiratory impedance measurements under the two measurement conditions. Secondary Objectives are to: i)evaluate the patient's comfort during the measurement with the cheek support and compare this comfort to the gold standard condition; ii) assess the maximum and minimum face dimensions of the recruited subjects that allow for effective and comfortable cheek support; iii) evaluate the type and frequency of measurement errors introduced by the use of the integrated cheek support in the mouthpiece.

This description comes directly from the study's public registry record.

Talk to the study team

Raffale Dellaca, PhD  ·  0223999005  ·  raffaele.dellaca@polimi.it

Chiara Veneroni, PhD  ·  0223999024  ·  chiara.veneroni@polimi.it

Always discuss trial participation with your own doctor first.

Locations (1)

Allergy and Pneumology Outpatient ClinicBergamo, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06537362