Rheumatology and circulation
Nailfold capillaroscopy: what the test shows in Raynaud's and connective tissue disease
Nailfold capillaroscopy, also called nailfold microscopy, is a test that lets doctors look closely at the small blood vessels in the fingers. It is one of several tests used when someone has Raynaud's phenomenon, to help tell primary Raynaud's from secondary Raynaud's linked with conditions such as scleroderma. This guide explains the test in context.
Last checked: 2026-10-10
Key facts
At a glance.
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What it looks at
Arthritis UK (formerly Versus Arthritis) describes a test that involves looking at tissue from a fingernail under a microscope so doctors can look closely at the small blood vessels in your fingers. It is called nailfold microscopy, or capillaroscopy.
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Used to tell types apart
Arthritis UK says tests for Raynaud's are carried out to tell apart the primary and secondary forms of the condition.
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Primary versus secondary
Primary Raynaud's occurs on its own and most people with it will not go on to develop further problems. Secondary Raynaud's is linked with conditions such as scleroderma and, less commonly, lupus.
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Not the only test
Other tests include blood tests, an X-ray to look for an extra rib at the base of the neck and, in some hospitals, a cold stress test, according to Arthritis UK.
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Raynaud's is common
The NHS describes Raynaud's as common and says it does not usually cause severe problems, though it can sometimes be a sign of a more serious condition.
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Raynaud's does not mean scleroderma
Arthritis UK says that having Raynaud's does not mean you will go on to develop scleroderma or another connective tissue disease.
What nailfold capillaroscopy is
Capillaries are the smallest blood vessels in the body. At the base of the fingernail they sit close to the surface, and this makes them accessible to a specialised microscope. Arthritis UK describes the test as one that involves looking at the tissue from a fingernail under a microscope, so doctors can look closely at the small blood vessels in the fingers. It is called nailfold microscopy or capillaroscopy.
The test is not described as painful in the sources used for this guide, and this page does not make claims about how it feels or how long it takes, because the pages read do not say. Ask the department carrying it out what to expect, including whether you should avoid nail polish or hand cream beforehand.
Why it is done: Raynaud's phenomenon
Raynaud's phenomenon is where blood stops flowing properly to the fingers and toes, usually in response to cold or stress. The NHS says the skin may turn white or paler, sometimes blue, and then red as blood flow returns, and that pain, numbness and pins and needles can occur. Attacks can last from a few minutes to a few hours.
Most Raynaud's is primary, which means it occurs on its own. Arthritis UK says primary Raynaud's is fairly common, affects more women than men and does not usually damage the fingers. Secondary Raynaud's is linked with another condition, most often scleroderma and less commonly lupus, and can be more severe, with ulcers at the fingertips in rare cases. Because the symptoms can look the same, doctors need ways of separating the two groups, and capillaroscopy is one of them.
The wider set of tests
Arthritis UK sets out several tests that may be carried out if Raynaud's is suspected and the diagnosis is in doubt. They are done to tell the primary and secondary forms apart, and they may need to be done at a hospital.
| Test | What it shows |
|---|---|
| Blood tests | Blood cell counts and other information that helps decide whether Raynaud's is primary or secondary |
| X-ray | Looks for an extra rib at the base of the neck (cervical rib), which can press on blood vessels to the arms |
| Nailfold microscopy (capillaroscopy) | A close look at the small blood vessels in the fingers |
| Cold stress test (thermography) | Records how long hands or feet take to return to normal temperature after cold water, used in some hospitals |
The link with scleroderma and other conditions
Scleroderma is the name the NHS gives to a range of autoimmune conditions that can cause hard, thickened areas of skin and sometimes problems with muscles, bones, internal organs and blood vessels. The two main types are localised scleroderma (morphoea) and systemic sclerosis. Limited cutaneous systemic sclerosis often starts as Raynaud's, according to the NHS, which is why Raynaud's that begins in adulthood or comes with other features gets a closer look.
The NHS advises seeing a GP if Raynaud's symptoms are very bad or getting worse, if they affect only one side of the body, if you also have joint pain, skin rashes or muscle weakness, if you are over 30 and get symptoms for the first time, or if a child under 12 has symptoms. A GP may arrange tests if Raynaud's could be a sign of a condition such as rheumatoid arthritis or lupus.
Arthritis UK reassures that if you have scleroderma it is likely you will get Raynaud's at some stage, but that having Raynaud's does not mean you will develop scleroderma or another connective tissue disease. It encourages getting a diagnosis early to find out whether Raynaud's is primary or secondary.
What happens after the test
Results are interpreted alongside your symptoms, examination and blood tests rather than on their own. Arthritis UK says your doctor will make a diagnosis based on your symptoms and the results of any tests. The sources read for this guide do not describe the specific patterns doctors look for on capillaroscopy, so this page does not either; a rheumatologist can explain what was seen in your own report.
Whatever the result, self-care is similar. The NHS suggests keeping your home warm, wearing warm clothes especially on the hands and feet, avoiding sudden changes in temperature, exercising regularly, not smoking and not having too much caffeine. A GP may prescribe a medicine such as nifedipine to improve circulation if symptoms are very bad or getting worse, and Arthritis UK describes drugs that widen blood vessels, with intravenous treatment reserved for severe cases, almost always secondary Raynaud's.
NHS pathway or private testing
On the NHS, a GP who suspects secondary Raynaud's may arrange tests, and Arthritis UK says some of them may need to be done at a hospital. Private rheumatology services may also offer tests and consultations, and a private specialist will usually want to see any earlier blood results and reports. Whichever route you use, ask for a written report that you can bring to any later appointment.
Frequently asked
Questions people ask.
Quick, plain-English answers to the questions we hear most.
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What is nailfold capillaroscopy?
Arthritis UK describes it as a test where tissue from a fingernail is looked at under a microscope so doctors can see the small blood vessels in your fingers. It is also called nailfold microscopy.
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Why would I need it?
It is one of the tests used to tell primary Raynaud's from secondary Raynaud's, which is linked with conditions such as scleroderma or lupus.
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Does it mean I have scleroderma?
No. Arthritis UK says that having Raynaud's does not mean you will go on to develop scleroderma or another connective tissue disease.
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What other tests might I have?
Blood tests, an X-ray to look for a cervical rib and, in some hospitals, a cold stress test, according to Arthritis UK.
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Who should be tested for secondary Raynaud's?
The NHS suggests seeing a GP if symptoms are on one side only, you have joint pain, rashes or muscle weakness, you are over 30 and it is new, or a child under 12 has symptoms.
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What is primary Raynaud's?
Arthritis UK says it occurs on its own, is fairly common, affects more women than men and does not usually damage the fingers. Most people will not go on to have further problems.
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Can Raynaud's be caused by medicines?
Yes. The NHS says it can be caused by certain medicines or working with vibrating tools, and Arthritis UK gives beta blockers as an example. Do not stop a medicine without asking your doctor.
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What can I do for Raynaud's myself?
The NHS suggests keeping warm, avoiding sudden temperature changes, exercising regularly, not smoking and limiting caffeine.
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Is there treatment?
A GP may prescribe nifedipine to improve circulation, according to the NHS. Arthritis UK also lists drugs that widen blood vessels, with intravenous treatment for severe cases.
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Where can I find support?
The NHS points to Scleroderma and Raynaud's UK (SRUK), a charity for people with scleroderma or Raynaud's.
Where this comes from
Sources and checking.
This guide is for information, not medical advice.
Your GP or consultant knows your history and can tell you which parts apply to you. If your symptoms are severe, rapidly worsening, or come with red-flag features, seek urgent medical care. Figures and availability change, so treat them as a guide and confirm with the provider.
Published 2026-10-10, next review 2027-10-10.
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Arthritis UK (formerly Versus Arthritis): Raynaud's phenomenon, https://versusarthritis.org/about-arthritis/conditions/raynauds-phenomenon/ , retrieved October 2026
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NHS: Raynaud's, https://www.nhs.uk/conditions/raynauds/ , retrieved October 2026
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NHS: Scleroderma, https://www.nhs.uk/conditions/scleroderma/ , retrieved October 2026
Related guides
Keep reading.
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Raynaud's phenomenon
Colour changes in the fingers and toes in the cold.
Read guide -
Scleroderma
Autoimmune conditions that thicken the skin.
Read guide -
Systemic sclerosis
The form of scleroderma that can affect internal organs.
Read guide -
Lupus
An autoimmune condition linked less commonly with Raynaud's.
Read guide