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Effects of SIMEOX on Flow and Volume

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Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Status

Withdrawn

Conditions

Healthy

Treatments

Device: SIMEOX

Study type

Interventional

Funder types

Other

Identifiers

NCT03655860
2018/08AOU/312 (Other Identifier)
SIMEOX-01

Details and patient eligibility

About

This study will investigate the effects of the SIMEOX (an airway clearance device) on flow and volume generated in healthy subjects

Full description

This is a pilot study assessing the effect of the SIMEOX device on flow and volume generated in healthy subjects.

Assessment of flow and volume will be performed before and during the application of the SIMEOX. Vital capacity and expiratory flow will be assessed.

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Able to understand the instructions

Exclusion criteria

  • Obesity (BMI > 30kg/m²)
  • Active smoker
  • Severe scoliosis
  • Cardiovascular ou neuromuscular disease

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

SIMEOX
Experimental group
Description:
Use of the device SIMEOX to exhale
Treatment:
Device: SIMEOX

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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