Stimulation of the Cervical Sympathetic Ganglion for Treatment of Asthma

Asthma Clinical Trial

Official title:

Stimulation of the Cervical Sympathetic Ganglion for Treatment of Asthma.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01724307
• Other study ID #: 2011H0009
• Status: Completed
• Phase: N/A
• First received: October 9, 2012
• Last updated: January 25, 2016
• Start date: September 2011
• Est. completion date: November 2013

Study information

• Verified date: January 2016
• Source: Ohio State University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate if stimulating the nerve involved with airway constriction, while undergoing procedures that are known to cause asthma exacerbations, decreases the level of asthma attack experienced.

Description:

Asthma is a chronic inflammatory disorder of the airways characterized by shortness of breath, wheezing, cough, and fatigue. Some people suffer from sudden worsening of asthma symptoms despite being treated with medications. When people have asthma attacks the muscle tissue in the airway contracts causing the airway to narrow and decreasing the ability for the person to breathe.

Neurological pacemakers are FDA approved devices that stimulate nerves in the body and have been used for the treatment of many disorders such as Parkinson's, epilepsy, chronic pain and urinary incontinence. Recent animal studies have shown that stimulating (activating a nerve) the carotid sheath area (located in the neck) can cause the rapid relaxation of the muscles which contract during an asthma attack. This approach has also been successfully used in patients at an emergency room when they came in with a severe asthma attack.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1
• Est. completion date: November 2013
• Est. primary completion date: November 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. All patients aged 18-70 years of age suffering from mild-to-moderate asthma who have either:

1. bronchial hyper-responsiveness to MCT

2. bronchial hyper-responsiveness to EVH testing

2. All patients with documented evidence of a positive MCT or EVH test within 36 months of Visit 1

3. Are capable of reading and understanding questionnaires and providing written informed consent.

4. Are willing and able to adhere to the study visit schedule and other protocol-specified procedures.

Exclusion Criteria:

1. Non-English speaking.

2. Subjects experiencing an exacerbation of asthma within 6 weeks of Visit 1

3. Subjects with a forced expiratory volume (FEV1) = 60% predicted, on spirometry

4. Subjects and medications:

1. Subjects allergic to methacholine or any other parasympathomimetic agent

2. Subjects on investigational drugs or participating in interventional research trial(s), 30 days prior to enrollment or during the duration of the study

3. Subjects currently on ß-adrenergic blockers or, a cholinesterase inhibitor

4. Prior to the administering of the MCT/ EVH test:

i) use of a short-acting bronchodilator (within 6hrs.) ii) use of a long-acting bronchodilator (within 36hrs.) iii) use of inhaled corticosteroids/ leukotriene modifiers (within 72hrs.) iv) exercise (within 4hrs.)

5. Subject smoking: in the last 6 months or a smoking history of >10 pack-years

6. Subjects who have experienced a febrile illness within 3 weeks of Visit 1

7. Subjects with a history of active poorly controlled epilepsy, cardiovascular disease (esp. with bradycardia), vagotonia, peptic ulcer disease, thyroid disease, or urinary tract obstruction or other chronic ailments that would interfere with the current study

8. Subjects who are pregnant or refuse medically acceptable contraception during the study period

9. Subjects with a history of >3 stellate ganglion block procedures

10. Subjects who have undergone surgical procedures involving the cervical spine

11. Evidence of coagulopathy with abnormal INR, PT/ PTT and platelet count

12. Subjects allergic to lidocaine (Subject may still participate in the study if they agree to the procedure without using the Lidoderm patch)

13. Subjects participating in another interventional research trial

14. Subjects with a condition or compliance issue, which in the investigator's opinion might interfere with participation in the current study

15. Subjects unable or unwilling to provide a written consent to undergo the required testing/ procedures/ physical exam or answer the questionnaires

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Asthma

Intervention

Procedure:
• Neurostimulation of stellate ganglion
An electrical nuerostimulation of the stellate ganglion up to 60 minutes

Locations

Country	Name	City	State
United States	The Ohio State University	Columbus	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Jonathan Parsons

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluate if neurostimulation of stellate ganglion modulates airway hyperresponsiveness to bronchoprovocation testing. Comparison of FEV1 drop before and after neurostimulation testing will be primary outcome measure	To determine whether neurostimulation of the stellate ganglion modulates airway hyperresponsiveness to bronchoprovocation testing in asthmatics	60 minutes post treatment	No
Secondary	Evaluate if neurostimulation of the stellate ganglion modulates airway inflammation	To determine whether neurostimulation of the stellate ganglion modulates airway inflammation as measured by exhaled nitric oxide in asthmatics	60 minutes post treatment	No