Idiopathic Pulmonary Fibrosis



What is IPF?

Idiopathic Pulmonary Fibrosis is when lung tissue becomes scarred and damaged without a known cause (idiopathic). The lungs become thick and stiff, making it difficult for your lungs to work properly, and as pulmonary fibrosis becomes worse it will become harder to breathe.

Conditions that contribute to IPF:

  • Environmental Factors such as asbestos exposure, silica dust, bird and animal droppings.
  • Radiation Treatments for cancer can cause some lung damage, depending on amount of exposure.
  • Medications that can damage your lungs may include: Chemotherapy, heart rhythm drugs, and some antibiotics.
  • Medical Conditions like: Pneumonia, Tuberculosis, Lupus, Scleroderma, Rheumatoid Arthritis, and Sarcoidosis.

The list of causes and conditions that can lead to pulmonary fibrosis is long. However, in most cases, the cause cannot be found, which is referred to as idiopathic or “unknown cause.

There are several theories about what might trigger idiopathic pulmonary fibrosis, including tobacco smoke and viruses. Because idiopathic pulmonary fibrosis has also been seen to run in families, genes or heredity may also be a factor.

Symptoms Include:

  • Shortness of breath (dyspnea)
  • A dry cough
  • Fatigue
  • Unexplained weight loss
  • Aching muscles and joints

IPF Clinical Trials

You may quality for a clinical research study for those suffering from Idiopathic Pulmonary Fibrosis.

Current Studies

You can read more about the IPF studies here:

Apply Online

If you are eligible and enroll, you will receive all study-related care at no cost. You will also receive monitoring of your IPF by a research doctor.

For more information call our office at (425) 225-2760.