A Study of Stellate Ganglion Block and / or Reserpine in Group 2 Pulmonary Hypertension

Sponsor

Mayo Clinic (Other)

Overall Status

Withdrawn

CT.gov ID

NCT02684786

Collaborator

(none)

Enrollment

Location

Arms

Study Details

Study Description

Brief Summary

Pulmonary hypertension Group 2 (PH 2) associated with left-sided heart disease is relatively common, is associated with a poor prognosis, and unfortunately there are no proven medical treatments beyond attempts at correcting the left sided heart disease. Many PH 2 patients have evidence of active constriction of blood vessels from increased nerve traffic. Use of agents or procedures which produce a reversible chemical blockage of this nerve traffic have not been systematically tested in PH 2. The investigators will test whether acute interruption of sympathetic nervous system tone, which local anesthetic block of the stellate ganglion in the neck, will improve PH2, and also test whether the high blood pressure drug reserpine, which blocks sympathetic nerve activity, will do so during a one month trial period.

Condition or Disease	Intervention/Treatment	Phase
Pulmonary Artery Hypertension	Drug: reserpine Procedure: stellate ganglion block Drug: lidocaine	Phase 1

Detailed Description

Background. Pulmonary hypertension Group 2 (PH 2) associated with left-sided heart disease is relatively common, is associated with a poor prognosis, and unfortunately there are no proven medical treatments beyond attempts at correcting the left sided heart disease. Many PH 2 patients have evidence of vasoconstriction and increased sympathetic nervous system activity. Use of agents or procedures which produce a reversible chemical sympathectomy have not been systematically tested in PH 2.

Methods. Two groups will be eligible for participation: Group 1 (n=10): Patients with PH 2 previously documented by echocardiography (echo), 6 minute walk test, biomarkers, and right heart catheterization (RHC) will receive reserpine, 0.05 mg per day for two weeks, then, 0.1 mg per day for an additional two weeks. After one month, patients will be reassessed for New York Heart Association (NYHA) class and drug side effects, echocardiography, 6 minute walk assessment, and brain natriuretic peptide (BNP). Group 2 patients (n=10) will have clinically suspected PH 2 and be scheduled to undergo clinically indicated RHC. If during RHC PH 2 is confirmed, after assessment of nitric oxide responsiveness, their baseline hemodynamics will be re-established over 10 minutes, and a left stellate ganglion block with lidocaine will be performed, and immediate hemodynamic responsiveness assessed. Four hours post-procedure, a side effect questionnaire will be obtained. Group 2 patients who complete RHC will then begin reserpine treatment in the same manner as Group I patients.

Hypothesis and Impact. PH 2 is the most common type of pulmonary hypertension. The current diagnostic and therapeutic strategy aims to treat the left sided heart disease in attempt to normalize pulmonary artery pressure. The place of selective pulmonary vasodilators is undefined. The investigator's approach addresses inhibition of adverse pulmonary vasoconstriction mediated by the sympathetic nervous system in PH 2.

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase I Study of Stellate Ganglion Block and / or Reserpine in Group 2 Pulmonary Hypertension

Actual Study Start Date :

Jul 1, 2016

Actual Primary Completion Date :

Jul 1, 2016

Actual Study Completion Date :

Jul 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Prior right heart catheterization Patients with qualifying hemodynamics from prior right heart catheterization will receive open label reserpine, 0.05 mg by mouth daily for two weeks, then 0.10 mg by mouth daily for two weeks, and then have repeat non-invasive assessments of status.	Drug: reserpine Patients with qualifying hemodynamics from prior right heart catheterization will receive open label reserpine, 0.05 mg by mouth daily for two weeks, then 0.10 mg by mouth daily for two weeks, and then have repeat non-invasive assessments of status
Experimental: Scheduled for right heart catheterization Patients with suspected group 2 pulmonary hypertension by clinical and non-invasive assessments and are scheduled to undergo clinically indicated right heart catheterization will have pulmonary artery pressures measured. If qualifying severity of group 2 pulmonary hypertension is present, after clinically indicated assessment of inhaled nitric oxide, their baseline hemodynamics will be allowed to re-equilibrate over 10 minutes, and then ultrasound guided left stellate ganglion block with lidocaine will be performed, and hemodynamics reassessed 10 minutes afterward	Procedure: stellate ganglion block Patients with suspected group 2 pulmonary hypertension by clinical and non-invasive assessments and are scheduled to undergo clinically indicated right heart catheterization will have pulmonary artery pressures measured. If qualifying severity of group 2 pulmonary hypertension is present, after clinically indicated assessment of inhaled nitric oxide, their baseline hemodynamics will be allowed to re-equilibrate over 10 minutes, and then ultrasound guided left stellate ganglion block with lidocaine will be performed, and hemodynamics reassessed 10 minutes afterward Drug: lidocaine Patients with suspected group 2 pulmonary hypertension by clinical and non-invasive assessments and are scheduled to undergo clinically indicated right heart catheterization will have pulmonary artery pressures measured. If qualifying severity of group 2 pulmonary hypertension is present, after clinically indicated assessment of inhaled nitric oxide, their baseline hemodynamics will be allowed to re-equilibrate over 10 minutes, and then ultrasound guided left stellate ganglion block with lidocaine will be performed, and hemodynamics reassessed 10 minutes afterward

Arm

Intervention/Treatment

Experimental: Prior right heart catheterization

Patients with qualifying hemodynamics from prior right heart catheterization will receive open label reserpine, 0.05 mg by mouth daily for two weeks, then 0.10 mg by mouth daily for two weeks, and then have repeat non-invasive assessments of status.

Drug: reserpine

Experimental: Scheduled for right heart catheterization

Patients with suspected group 2 pulmonary hypertension by clinical and non-invasive assessments and are scheduled to undergo clinically indicated right heart catheterization will have pulmonary artery pressures measured. If qualifying severity of group 2 pulmonary hypertension is present, after clinically indicated assessment of inhaled nitric oxide, their baseline hemodynamics will be allowed to re-equilibrate over 10 minutes, and then ultrasound guided left stellate ganglion block with lidocaine will be performed, and hemodynamics reassessed 10 minutes afterward

Procedure: stellate ganglion block

Drug: lidocaine

Outcome Measures

Primary Outcome Measures

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 [one month]
Adverse events of interest are for stellate ganglion block: pulmonary edema, bradycardia requiring treatment, hypotension requiring treatment, arrhythmia, pneumothorax, hoarseness, dysphagia, globus, left upper extremity weakness. For reserpine, heart failure hospitalization, syncope, all cause hospitalization, bradycardia requiring treatment, hypotension requiring treatment, new arrhythmia, edema requiring an increase in diuretics, depression, lethargy, nasal stuffiness, dizziness, orthostatic hypotension, falls, nightmares, sexual dysfunction, anxiety, dyspepsia. Adverse events classed as serious: Life threatening serious adverse events including acute coronary syndrome with active ischemia, fatal arrhythmias, myocardial infarction, acute kidney injury, cardiogenic shock, stroke, pulmonary embolization, arterial and/or venous thrombosis, systemic embolization, severe hypotension, respiratory failure and death Prolonged hospitalization or rehospitalization

Secondary Outcome Measures

Number of participants with successful stellate ganglion block [One hour]
Stellate block: frequency of the occurrence of ptosis and conjunctival flushing.
Effect of stellate ganglion block on heart rate [One hour]
Heart rate before and after stellate ganglion block
Change in 6 minute walk distance from one month of reserpine therapy [One month]
Six minute walk distance, meters, baseline compared to one month
Change in brain natriuretic peptide (BNP) from one month of reserpine therapy [One month]
BNP, pg/ml, baseline compared to one month
Change in Doppler derived mean pulmonary artery pressure from one month of reserpine therapy [One month]
Mean pulmonary artery pressure estimate, mm Hg
Change in blood pressure from one month of reserpine therapy [One month]
Blood pressure, mm Hg, baseline versus one month
Change in Minnesota Living with heart failure questionnaire from one month of reserpine therapy [One month]
Minnesota Living with heart failure questionnaire aggregate score, baseline versus one month
Hemodynamic effect of stellate ganglion block [One hour]
Blood pressure, mm Hg, before and after stellate ganglion block
Hemodynamic effect of stellate ganglion block [One hour]
Pulmonary artery pressure, mm Hg, before and after stellate ganglion block
Hemodynamic effect of stellate ganglion block [One hour]
Pulmonary capillary wedge pressure, mm Hg, before and after stellate ganglion block
Hemodynamic effect of stellate ganglion block [One hour]
right atrial pressure, mm Hg, before and after stellate ganglion block
Hemodynamic effect of stellate ganglion block [One hour]
Cardiac output, liters per minute, before and after stellate ganglion block
Change in heart rate from one month of reserpine therapy [One month]
Heart rate, baseline versus one month

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 100 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion criteria:

Prior right heart catheterization, with mean pulmonary artery pressure > 25 mm Hg, pulmonary capillary wedge pressure > 15 mm Hg, and diastolic pressure gradient (pulmonary artery diastolic pressure - mean pulmonary capillary wedge pressure) ≥ 7 mm Hg OR clinically suspected group 2 pulmonary hypertension from non-invasive testing with planned right heart catheterization (RHC).
On stable diuretic therapy
Able to attend end-study visit 4 weeks after study entry

Exclusion criteria:

Anticipated surgery to correct heart lesion responsible for pulmonary hypertension
Need for heparinization for right heart catheterization (not standard practice, but sometimes utilized)
History of depression, or treatment with tricyclic anti-depressant, serotonin uptake inhibitor, monamine oxidase inhibitor
Severe renal or hepatic impairment, creatinine clearance < 30 ml/minute or renal replacement therapy or post-kidney transplant, abnormal liver function with elevated enzymes> 1.5 times the upper limit of normal or prior liver transplant.
Systolic blood pressure <100 mm Hg
Heart rate < 60 beats per minute
Inability to independently complete telephone follow-up at two weeks, and clinic end-study visit at 4 weeks.
Pulmonary edema
Infiltrative cardiomyopathy - amyloidosis
Symptomatic orthostatic hypotension
Women of childbearing age who have not had surgical sterilization and are not using oral contraceptives, or who's spouse has not had surgical sterilization will be excluded due to the length of the trial and the possibility that they could become pregnant after entry.
Uncontrolled heartburn
Prior surgery to the left neck, for example, carotid endarterectomy, or other surgery which would increase the risk of stellate ganglion block
Known sensitivity, allergy, or contraindication to lidocaine, any local anesthetic, or reserpine