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Not yet recruitingNCT07443124IMPACTUpdated Mar 2, 2026

Simeox 200 US Study

An interventional study of Intermittent intrapulmonary deflation in Bronchiectasis and Mucus; Plug, sponsored by Inogen Inc.. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-03-02.

Sponsored by Inogen Inc. · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
35
Allocation
Not applicable
Ages
18 Years to 85 Years
Sex
All
01

Study summary

The purpose of this single arm post-market observational study is to evaluate the short-term effectiveness of the Simeox 200 airway clearance device in improving airway clearance in adult patients aged 18 to 85 with bronchiectasis and chronic mucus hypersecretion. The study aims to establish a baseline for wet sputum weight production using the Simeox 200 device. Additionally, the study aims to assess the short-term effects of Simeox 200 on various outcomes, including lung function, respiratory symptoms, and health-related quality of life.

The study participants will undergo the following steps:

  1. Baseline Visit (V0): Participants will attend a baseline visit for eligibility screening, consent, a physical exam, and baseline assessments of various relevant parameters such as lung function, SpO2, and Patient-Reported-Outcomes.
  2. Treatment Sessions (V1): Participants will perform two supervised treatment sessions with the Simeox 200 device at the clinic, during which sputum will be collected and weighed.
  3. Home Use : Participants will use the device at home twice daily for 2 weeks, recording their usage and symptoms in a daily electronic diary.
  4. Final Clinic Visit (V2): Participants will return for a final clinic visit for repeat assessments.
  5. Follow-up Phone Call (14 days after V2): Participants will receive a follow-up phone call to assess ongoing symptoms and health status.
Read the detailed description

Airway clearance techniques (ACTs) are essential for removing excess bronchial secretions and preventing airway complications. However, their effectiveness relies on patient adherence and satisfaction. Simoex 200 is a novel airway clearance device that uses intermittent negative oscillating pressure to mobilize airway secretions from different parts of the lungs to central airways, facilitating expectoration. Preliminary studies in Europe on patients with chronic muco-obstructive lung diseases have demonstrated the effectiveness and good tolerance of previous generations of the device. This pilot study will evaluate the Simeox 200 device in a home care setting for patients with bronchiectasis and excessive mucus production. The results of this study will inform a future larger-scale clinical trial.

02

Conditions studied

  • Bronchiectasis
  • Mucus; Plug

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Keywords

  • Bronchiectasis
  • Mucus hypersecretion
  • Airway clearance technique
  • Bronchial drainage
03

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Diagnosis of bronchiectasis confirmed by computed chest tomography (CT chest) performed within the prior 36 months
  2. Persistent productive cough for which daily airway clearance therapy is prescribed.
  3. Daily sputum production estimated at > 1 tsp or 5 ml
  4. Clinically stable on medical regimen with no pulmonary exacerbation in the past 4 weeks prior to study enrolment
  5. Subject able to sign informed consent

Exclusion criteria

Exclusion Criteria:

  1. Inability to cough forcefully and independently, as determined by the clinician
  2. Ventilatory assistance with endotracheal tube, tracheostomy tube, or mask (not including nocturnal CPAP)
  3. Neuromuscular disease with muscle respiratory weakness
  4. Severe restrictive lung disease defined as Forced Vital Capacity (FVC) \<60% of predicted
  5. Unstable cardiac disease (e.g. major cardiac arrhythmia, unstable heart failure, heart attack, unstable angina)
  6. Hemodynamic instability, as determined by the clinician
  7. Airway at risk for aspiration, as determined by the clinician
  8. Uncontrolled gastroesophageal reflux disease (GERD) as determined by the clinician
  9. Upper airway surgery in the prior 3 months
  10. Cardiothoracic surgery, including esophageal surgery, in the prior 6 months
  11. Anticipated hospitalization within the next 2 weeks
  12. History of pneumothorax within the prior 6 months
  13. History of haemoptysis treated with embolization within the prior 12 months
  14. Inability to use airway clearance therapy as directed
  15. Unable or unwilling to complete study visits or provide follow-up data as required per the study protocol
  16. Pregnant or lactating female
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
35 participants (estimated)

Study arms

  • Experimental
    Simeox 200

    Simeox 200 airway clearance device

    Device: Intermittent intrapulmonary deflation

Interventions

  • DeviceIntermittent intrapulmonary deflation

    Two treatment sessions daily for two weeks

05

What researchers measure

Primary outcomes

  1. Wet sputum weight collected with Simeox 200 during device training visit

    Patients will be instructed during device training visit (V1) to spill all sputum into a pre-weighed pot from at least two supervised sessions. Immediately after collection, all sputum will be weighed on weighing scales with an accuracy of 0.01 grams.

    Time frame: From the first training session to the last, and up to one hour following each treatment session the day of training device visit.

Secondary outcomes

  1. Change from baseline in Forced Expiratory Volume in One seconde (FEV1) at the final study visit (V2) after 14 days of treatment

    FEV1will be measured with a spirometer according to the ATS guidelines immediately before any procedures at the study site

    Time frame: From enrollment to the final study visit at 15 days

  2. Change from baseline in Forced Vital Capacity (FVC) at the final study visit after 14 days of treatment

    FVC will be measured with a spirometer according to the ATS guidelines immediately before any procedures at the study site

    Time frame: From enrollment to the final study visit at 15 days

  3. Change from baseline in Forced Expiratory Flow between 25% and 75% of vital capacity (FEF25-75%) at the final study visit after 14 days of treatment

    FEF25-75% will be measured with a spirometer according to the ATS guidelines immediately before any procedures at the study site

    Time frame: From enrollment to the final study visit at 15 days

  4. Change from baseline in Peripheral blood oxygen saturation (SpO2) at final study visit after 14 days of treatment

    SpO2 will be measured transcutaneously at rest with a fingertip pulse oximeter before lung function measurements at rest and any procedures with the device at the study site

    Time frame: From enrollment to the final study visit at 15 days

  5. Change from baseline in perceived respiratory symptoms assessed with the Breathlessness, Cough and Sputum Scale (BCSS) at 7 and 14 days of treatment

    BCSS is a patient-reported outcome measure that asks patients to rate the severity of the three symptoms breathing difficulty, cough, and sputum levels, each on a 5-point scale from 0 (no symptom) to 4 (highest severe symptom)

    Time frame: From enrollment to 7 and 14 days of treatment at home

  6. The change from device training visit in wet sputum weight at the final study visit after 14 days of treatment

    Patients will be instructed to spill all sputum into a pre-weighed pot. Immediately after collection, all sputum will be weighed on weighing scales with an accuracy of 0.01 grams.

    Time frame: From device training visit to the final study visit at 15 days

  7. The change from baseline in airway-disease health status assessed by the Chronic Airway Assessement Test (CAAT) and QOL - B questionnaire at the final study visit after 14 days of treatment

    The CAAT is an 8-item questionnaire designed for assessing the impact of a chronic respiratory disease such as bronchiectasis on a person's life. The questionnaire covers symptoms (such as cough, sputum, chest tightness and breathlessness) and disease impacts (including physical activity, confidence, sleep and energy) assessed each on a 6-point scale from 0 (best outcome) to 5 (worst outcome). The QOL-B on the other hand is a self-administered, patient-reported outcome measure assessing symptoms, functioning and health-related quality of life for patients bronchiectasis.

    Time frame: From enrollment to the final study visit at 15 days

  8. The change from baseline in walking distance assessed with 6-minutes Walking Test (6MWT) at the final study visit after 14 days of treatment

    The 6MWT is a low-intensity, submaximal exercise test used to assess aerobic capacity and endurance and oxygen saturation. 6MWT will be performed after spirometry assessment and in accordance with ATS guidelines. SpO2 will be measured transcutaneously at rest for 5 min before, during and at the end of the 6MWT. A modified Borg scale will be completed beofre and at the end of 6MWT for dyspnea and fatigability scores.

    Time frame: From enrollment to the final study visit at 15 days

  9. The change from baseline in borg dyspnea and fatigue score after 6MWT compared to borg dyspnea and fatigue score after 6MWT at the final study visit after 14 days of treatment respectively.

    The 6MWT is a low-intensity, submaximal exercise test used to assess aerobic capacity and endurance and oxygen saturation. 6MWT will be performed after spirometry assessment and in accordance with ATS guidelines. SpO2 will be measured transcutaneously at rest for 5 min before, during and at the end of the 6MWT. A modified Borg scale will be completed before and at the end of 6MWT for dyspnea and fatigability scores.

    Time frame: From enrollment to the final study visit at 15 days

  10. The global patient satisfaction will be evaluated with Lickert scale at the final study visit after 14 days of treatment

    Likert scale measures respondents' level of agreement/satisfaction or disagreement/dissatisfaction towards the treatment on the following attributes: overall / learning time / easy to handle / subjective effectiveness / treatment duration / use in autonomy. These rating scales offer 10 response options, ranging from 0 (worst outcome) to 10 (best outcome).

    Time frame: At the final study visit at 15 days

  11. Adherence to the device over the entire period of home use

    The patient will record adherence to Simeox 200 on a daily diary at home, noting the number of sessions per day and the duration of each session.

    Time frame: From the first day of device use at home to the 14 days of home treatment

06

Study locations

1 site
  • Medical University of South Carolina
    Charleston, South Carolina 29425, United States
    • Patrick A Flume, MD · Contact · xxx-xxx-xxxx
07

References and documents

Individual participant data

Plan to share: Undecided — Plan has not been decided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07443124
Lead sponsor
Inogen Inc.
Responsible party
Sponsor
First posted
Mar 2, 2026
Start date
Feb 2026 (estimated)
Primary completion
May 2026 (estimated)
Completion
Jun 2026 (estimated)
Last update
Mar 2, 2026

Study contacts

Roxanna Edwards
Contact
redwards@inogen.net
xxx-xxx-xxxx
Chief Medical Officer
Contact
kjhaveri@inogen.net
Patrick A Flume, MD
principal investigator · Medical University of South Carolina

Oversight

FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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