PROPEL® Patient Stories
Many people have benefited from PROPEL® sinus stents. There are countless success stories showing it to be a safe and effective solution that can improve the results of sinus surgery. Here are a few examples of what patients are saying.
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The accounts given are genuine and documented. Each video represents a unique individual experience and does not provide any indication, guide, warranty or guarantee as to the response other people may have to the PROPEL sinus implant. Comparative claims made by individuals are the opinion of the individual alone and do not constitute the views of Intersect ENT. To date, Intersect ENT has not conducted research comparing PROPEL to other therapies. Physicians should use their own clinical judgment when deciding how to treat sinusitis.
The PROPEL sinus implants are intended for use following sinus surgery to maintain the sinus openings and to locally deliver a drug to the sinuses: PROPEL for use in the ethmoid sinus, PROPEL Mini for use in the ethmoid sinus and frontal sinus opening and PROPEL Contour for use in the frontal and maxillary sinus openings. The products are intended for use in patients ≥18 years of age. These products are not intended for people who are allergic to the drug (mometasone furoate) or to certain polymers. Safety and effectiveness of the implant in pregnant or nursing females have not been studied. Risks may include, but are not limited to, pain/pressure, movement of the implant (within or out of the sinus), possible side effects of the drug, infection, and nose bleed. For more information on the risks and benefits of PROPEL sinus implants, please talk to your doctor. The FDA approved labeling can be found at www.IntersectENT.com. Rx only.
INTERSECT ENT and PROPEL are registered trademarks of Intersect ENT, Inc. in the United States and other countries.
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