Effects of SIMEOX on Flow and Volume

Not Applicable

Withdrawn

• Conditions: Healthy
• Interventions: Device: SIMEOX

• Registration Number: NCT03655860
• Lead Sponsor: Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Brief Summary

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

Detailed 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.

Study Timeline

• Study First Submitted: 2018-08-28
• Study First Submitted QC: 2018-08-30
• Study First Posted: 2018-08-31
• Study Start: 2018-09-15
• Primary Completion: 2021-12-30
• Study Completion: 2021-12-30
• Status Verified: 2023-11
• Last Update Submitted: 2023-11-22
• Last Update Posted: 2023-11-28

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Able to understand the instructions

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
SIMEOX	SIMEOX	Use of the device SIMEOX to exhale

Primary Outcome Measures

Name	Time	Method
Change in expiratory volume	5min	Expiratory volume before and during the use of the SIMEOX will be compared
Change in expiratory volume flow rate	5min	Expiratory flow rate before and during the use of the SIMEOX will be compared

Trial Locations

Locations (1)

William Poncin; 🇧🇪 Brussels, Belgium