Fenzian Asthma Multicenter Outcomes Study

Not Applicable

Completed

Conditions: Asthma

Interventions: Device: Fenzian Device
Device: Sham Device

Registration Number: NCT00784758

Lead Sponsor: University of California, Los Angeles

Brief Summary: The purpose of this study is to investigate the effects of Fenzian™ treatment on symptoms (such as shortness of breath), lung function (how well the lungs work), and albuterol/salbutamol (rescue medication) use in people with asthma. This will be done by comparing the effects of Fenzian™ treatment to the effects of a sham treatment, which looks the same as the Fenzian™ device but doesn't do anything.

The Fenzian™ device is an electrical instrument that the investigators hope will help reduce airway inflammation associated with asthma symptoms by stimulating the nerves with very low electrical currents. The study device will be applied directly to the skin on the back, working along the ribs toward the spine, alternating between left and right sides, and on your face.

Detailed Description: Not available

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 81

Inclusion Criteria

Ages 12-80 years. [NOTE: Only the Johns Hopkins site will enroll subjects under 18.]
Clinical history consistent with asthma (GINA 4 definitions) for at least six months
Current symptoms and features of partly-controlled or uncontrolled asthma, according to GINA classification of asthma control
A stable (1 month) treatment regimen consisting of:
- as needed short-acting bronchodilators alone,
- as needed short-acting bronchodilators in combination with low- or medium-dose inhaled corticosteroids (<= 1000 mcg per day beclomethasone or equivalent,
- any combination of long acting beta-agonist bronchodilator and low- or medium-dose inhaled corticosteroid (as defined above),as needed short-acting bronchodilators in combination with montelukast or other leukotriene modifier
Willingness to comply with the study protocol and ability to perform the study procedures.
Willingness to attend the study site according to the specified treatment schedule

Inclusion Criteria Assessed at Visit 1:

Pre-bronchodilator forced expiratory volume at one second (FEV1) between 60% predicted and the lower limit of normal.
Pre-bronchodilator [FEV1/forced vital capacity (FVC)] less than the lower limit of normal.
Reversibility of FEV1 of at least 200 ml, 15-20 minutes after 4 puffs of albuterol HFA pressurized metered-dose inhaler pMDI.

Inclusion Criteria Assessed at Visit 2:

Reversibility of FEV1 of at least 200ml, 15-30 minutes after 4 puffs of albuterol HFA pressurized metered-dose inhaler (pMDI) if not confirmed at Visit 1 plus
Using short-acting bronchodilator therapy on two or more occasions in each of the two weeks preceding Visit 2 plus (Ventolin HFA counter decrease of at least 8 puffs)
Partly controlled or uncontrolled of asthma as indicated by one to three, but not four of the following in each of the two weeks preceding Visit 2:
- Daytime symptoms more than twice per week
- Any limitation of activity
- Any nocturnal symptoms or awakening
- peak expiratory flow (PEF)<80% of predicted on any day

Exclusion Criteria

Pulmonary disease other than asthma, such as smoking-related chronic obstructive pulmonary disease (COPD), clinically significant bronchiectasis, lung resection, and interstitial lung disease.
Other significant systemic illness which might, in the opinion of the investigator alter the risk or outcome of the study (e.g. cardiovascular arrhythmias or conduction abnormalities, hyperthyroidism, uncontrolled hypertension, cancer)
Tobacco smoking greater than 10 pack-year of cumulative exposure or current smoking within 10 years.
Respiratory tract infection within 6 weeks of the study.
Seasonal allergies causing symptoms within the past 4 weeks. Perennial or out of season allergic rhinitis is acceptable. Nasal corticosteroids and long-acting antihistamines are acceptable.
Any investigational drug or treatment within 30 days.
Use of cromolyn, nedocromil, theophylline, tiotropium, or oral albuterol within 1 week prior to Visit 1 of the study.
Current use of omalizumab or within the last 8 weeks.
Subjects on anti-depressant (mono-amine oxidase inhibitors or tricyclic antidepressants) treatment within 8 weeks.
Non-potassium sparing diuretics unless in fixed combination with potassium-sparing diuretics within one week.
Digoxin, within one week, unless levels have been monitored previously while taking albuterol or long-acting beta2-agonist (LABAs).
Presence of an implanted cardiac pacemaker or neurostimulator. A removable transcutaneous nerve stimulator, not used during the treatment sessions is acceptable.
Non-selective beta agonists. (acceptable choices include: bisprolol, betaxolol, atenolol, acebutolol and metoprolol)
Subjects who are pregnant or breast feeding.
Persons employed by or related to those employed by the investigative site (e.g. Pulmonary Division).
Prior Fenzian treatment for any indication
Hypersensitivity or intolerance of albuterol HFA pMDI (Ventolin) or its components. Note: if the subject is using ipratropium bromide for rescue short-acting bronchodilator, they must specifically not have been placed on that treatment due to intolerance of albuterol/salbutamol.
Inability to withhold, before and during each visit (except the initial consent visit), xanthine-containing foods (coffee, tea, cola, chocolate, etc.) and alcohol for 6 hours, and short-acting bronchodilators for 8 hours.
Unwillingness to stop use of non-study supplied albuterol (nebulized, chlorofluorocarbon (CFC) or HFA), other short-acting beta agonists (e.g. epinephrine, levalbuterol, metaproterenol, pirbuterol, terbutaline) and ipratropium during the study (after consent through visit 4).
Inability to coordinate the timing for doses of long-acting beta agonists (withhold period at least 12 hours prior to visit) with Visits 1, 2, 3 or 4

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Fenzian Device	Fenzian Device	Subjects randomized to this arm will receive treatment with the Fenzian Device
Sham Device	Sham Device	Subjects randomized to this arm will receive treatment with the sham device.

Primary Outcome Measures

Name	Time	Method
Change in Asthma Control Questionnaire (ACQ) 7 Score	Baseline to completion of treatment at 9 weeks	Asthma Control Questionnaire (QOL Technologies 2004) Elizabeth Juniper, (Eur Respir J 1999; 14:902-7). Range 0-6, 0 is no symptoms, 6 is maximal symptoms. 0.5 is considered a minimally important difference, 0.75 or less is associated with a 85% chance that the subject's asthma is well controlled, 1.50 or greater is associated with a 88% chance that the subject's asthma is not well controlled. The ACQ consists of 6 patient/subject reported questions on symptoms and a question completed by the staff for categorization of the patient/subjects forced expiratory volume in the first second (FEV1) from spirometry.

Secondary Outcome Measures

Name	Time	Method
Change in Sino-Nasal Outcome Test (SNOT-22) - Total Score	Baseline to completion of treatment at 9 weeks	The SNOT-22 is a disease-specific quality of life score for rhinosinusitis. SNOT22 is a validated scale which measures sinonasal symptoms for sinusitis patients. The 22 questions are rated on a scale of 0-5 for a maximum total score of 110. Higher scores represent more symptomatic patients.
Change in SNOT-22 Nasal Sub-score	Baseline to completion of treatment at 9 weeks	Sino-nasal outcome test-22 nasal sub-score. The nasal subscore consists of 8 questions, each on a scale of 0 (no problems) to 5 (as bad as it can be). Higher scores indicate worse symptoms of rhinosinusitis.
Daytime Symptom Score	7 days prior to final assessment visit at week 15	Daytime symptoms due to asthma were assessed via the electronic diary (AM2+ Asthma Monitor) each evening for 7 days prior to the study visit at Week 15. Daily scores were derived from five questions relating to 1) frequency of asthma symptoms, 2) impact of asthma symptoms, 3) activity, 4) impact of asthma on activity, and 5) breathlessness. Each question was scored from 0 (best) to 6 (worst), with the average of 5 questions providing a daily score ranging from 0 (best) to 6 (worst). Each participant's symptom score was calculated as the average of 7 daily scores. Thus, the range of possible scores is from 0 (best) to 6 (worst).
Change in Transition Dyspnea Index (TDI) - Functional Impairment	Baseline to completion of treatment at 9 weeks	The TDI is an interviewer-administered instrument which measures the changes in the participant's dyspnea from Baseline. The scores in the TDI evaluate ratings for 3 different categories (functional impairment, magnitude of task in exertional capacity, and magnitude of effort). TDI category scores range from -3 (major deterioration) to +3 (major improvement)
Change in Transition Dyspnea Index - Magnitude of Task at Visit 3	Baseline to completion of treatment at 9 weeks	The TDI is an interviewer-administered instrument which measures the changes in the participant's dyspnea from Baseline. The scores in the TDI evaluate ratings for 3 different categories (functional impairment, magnitude of task in exertional capacity, and magnitude of effort). TDI category scores range from -3 (major deterioration) to +3 (major improvement)
Change in Transition Dyspnea Index - Magnitude of Effort at Visit 3	Baseline to completion of treatment at 9 weeks	The TDI is an interviewer-administered instrument which measures the changes in the participant's dyspnea from Baseline. The scores in the TDI evaluate ratings for 3 different categories (functional impairment, magnitude of task in exertional capacity, and magnitude of effort). TDI category scores range from -3 (major deterioration) to +3 (major improvement)
Change in Transition Dyspnea Index - Functional Impairment	Baseline to final assessment visit (15 weeks)	The TDI is an interviewer-administered instrument which measures the changes in the participant's dyspnea from Baseline. The scores in the TDI evaluate ratings for 3 different categories (functional impairment, magnitude of task in exertional capacity, and magnitude of effort). TDI category scores range from -3 (major deterioration) to +3 (major improvement)
Change in Transition Dyspnea Index - Magnitude of Effort	Baseline to final assessment visit (15 weeks)	The TDI is an interviewer-administered instrument which measures the changes in the participant's dyspnea from Baseline. The scores in the TDI evaluate ratings for 3 different categories (functional impairment, magnitude of task in exertional capacity, and magnitude of effort). TDI category scores range from -3 (major deterioration) to +3 (major improvement)
Change in Transition Dyspnea Index - Magnitude of Task	Baseline to final assessment visit (15 weeks)	The TDI is an interviewer-administered instrument which measures the changes in the participant's dyspnea from Baseline. The scores in the TDI evaluate ratings for 3 different categories (functional impairment, magnitude of task in exertional capacity, and magnitude of effort). TDI category scores range from -3 (major deterioration) to +3 (major improvement)
Daily Short-acting Bronchodilator (Albuterol/Salbutamol) Use	2 weeks after completion of treatment (weeks 9-11)	Daily short-acting bronchodilator use during the 2 weeks, modeled as a zero-modified negative binomial (usually 2 puffs/day)
Short-acting Bronchodilator (Albuterol/Salbutamol) Free Days	2 weeks after completion of treatment (weeks 10 -11)	Percent of rescue-free days during a two week period after completing treatment phase
Change in Asthma Control Questionnaire 6 Score	Baseline to completion of treatment at 9 weeks	Asthma Control Questionnaire (QOL Technologies 2004) Elizabeth Juniper, (Eur Respir J 1999; 14:902-7). Range 0-6, 0 is no symptoms, 6 is maximal symptoms. 0.5 is considered a minimally important difference, 0.75 or less is associated with a 85% chance that the subject's asthma is well controlled, 1.50 or greater is associated with a 88% chance that the subject's asthma is not well controlled. The ACQ consists of 6 patient/subject reported questions on symptoms.
Change in Spirometry - FEV1	Baseline to completion of treatment at 9 weeks
Change in Spirometry - Forced Vital Capacity (FVC)	Baseline to completion of treatment at 9 weeks
Change in Spirometry - FEV1/FVC	Baseline to completion of treatment at 9 weeks
Change in Spirometry FEF25-75%	Baseline to completion of treatment at 9 weeks	A measure of forced expiratory flow between 25% and 75% of FVC (FEF25-75%)
Change in Asthma Control Test Score	Baseline to completion of treatment at 9 weeks	The Asthma Control Test is a 5-item questionnaire using 1-5 point Likert scales; maximum score 25 = complete control of asthma; minimum score 5 = poor control of asthma.
Change in Mini Asthma Quality of Life Questionnaire (AQLQ) Score (to Evaluate Quality of Life)	Baseline to completion of treatment at 9 weeks	The mini AQLQ is a questionnaire specifically designed to assess health status in patients with asthma. The mini-AQLQ consists of 15 questions covering symptoms and activities. Each question is scaled from 1 (poorly controlled asthma) to 7(maximally controlled asthma) where 7 reflects a higher quality of life. Total score is the sum of 15 items and may range from 15-105. An increase in the AQLQ score indicates a better quality of life.

Trial Locations

Locations (6): Addenbrookes NHS Trust, Cambridge University
🇬🇧
Bottisham, Cambridgeshire, United Kingdom
London Chest Hospital
🇬🇧
London, England, United Kingdom
Johns Hopkins University
🇺🇸
Baltimore, Maryland, United States
University of California, Los Angeles
🇺🇸
Los Angeles, California, United States
Duke University Medical Center
🇺🇸
Durham, North Carolina, United States
University of Cape Town Lung Institute
🇿🇦
Mowbray, Cape Town, South Africa