Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06401291

Transcutaneous Electrical Nerve Stimulation in Patients With Angina and Non-Obstructive Coronary Arteries

Led by Catharina Ziekenhuis Eindhoven · Updated on 2024-05-06

20

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In patients with angina pectoris undergoing a coronary angiography (CAG) up to 40% do not have obstructive coronary artery disease (CAD). The majority of patients with no obstructive CAD are women with a frequency of up to 70% compared to 50% in men. These patients are diagnosed as having angina and non-obstructive coronary arteries (ANOCA). There are two endotypes of ANOCA. The first endotype is microvascular angina (MVA) caused by a combination of structural microcirculatory remodelling and functional arteriolar dysregulation, also called coronary microvascular dysfunction (CMD). The second endotype is vasospastic angina (VSA) caused by epicardial coronary artery spasm that occurs when a hyper-reactive epicardial coronary segment is exposed to a vasoconstrictor stimulus. Both endotypes of ANOCA are associated with significantly greater one-year risk of myocardial infarction (MI) and all-cause mortality, have a significantly impaired quality of life and have a high health care resource utilisation. The current treatment for ANOCA consists of three aspects. The first aspect is managing lifestyle factors such as weight management, smoking cessation and exercise. The second aspect is managing known cardiovascular risk factors such as hypertension, dyslipidaemia and diabetes mellitus. And the third aspect is antianginal medication. In both endotypes ACE inhibitors or angiotensin II receptor blockers should be considered. In MVA the antianginal medication that can be used are betablocker, calcium channel blocker, nicorandil, ranolazine, ivabradine and/or trimetazidine. In VSA calcium channel blocker, long-acting nitrate and/or nicorandil can be initiated as antianginal therapy. Despite these treatment option approximately 25% of ANOCA patients have refractory angina symptoms. A possible treatment modality for ANOCA patients with refractory angina pectoris is spinal cord stimulation (SCS) or transcutaneous electrical nerve stimulation (TENS). Previous research (in patients with cardiac syndrome X) has shown that SCS improves time until angina and ischaemia, significantly less angina and an improvement in quality of life. These findings suggest that SCS and/or TENS could be a possible treatment modality for patients with ANOCA. The aim of this pilot study is to investigate whether treatment with TENS during a one month period leads to a significant reduction of angina pectoris and therefore a significant improvement in quality of life in patients with proven ANOCA, encompassing both endotypes (MVA and VSA).

CONDITIONS

Official Title

Transcutaneous Electrical Nerve Stimulation in Patients With Angina and Non-Obstructive Coronary Arteries

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Angina and no obstructive coronary artery disease (ANOCA) with Canadian Cardiovascular Society (CCS) class III or IV symptoms
  • Diagnosis of microvascular angina (MVA) with FFR > 0.8, CFR < 2.0, and IMR 25 25
  • Diagnosis of vasospastic angina (VSA) with FFR > 0.8, CFR 25 2.0, IMR < 25, and 25 90% diameter reduction plus angina and ischaemic ECG changes during acetylcholine testing
  • Persistent angina despite optimal medical therapy: for MVA, use of beta blockers, calcium channel blockers, nicorandil, and/or ivabradine; for VSA, use of calcium channel blockers, long-acting nitrates, and/or nicorandil at maximum tolerated dose
  • Age over 18 years
Not Eligible

You will not qualify if you...

  • Presence of both vasospastic angina and microvascular angina based on coronary function testing
  • Inability to provide informed consent
  • Inability to perform a 6-minute walking test
  • Presence of cardiac implanted electronic device such as pacemaker or implantable cardiac defibrillator
  • Presence of a spinal cord stimulator for other conditions such as complex regional pain syndrome or failed back surgery syndrome

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Catharina Hospital

Eindhoven, North Brabant, Netherlands, 5623EJ

Actively Recruiting

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Research Team

I

Inge Wijnbergen, MD, PhD

CONTACT

F

Fabienne Vervaat, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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