Known as renal denervation, the process involves inserting a catheter into a patient's arteries and delivering radiofrequency energy that inactivates kidney nerves.
It was believed to offer a pathway to lowering blood pressure by interrupting electrical signals to and from the kidney, an organ that is a key player in regulating blood pressure.
It has been approved for use in 80 countries, but is still considered experimental in the United States.
In other words, the real thing did not lower their blood pressure any better than a placebo.
The findings were published in the New England Journal of Medicine, and were presented at the American College of Cardiology annual meeting.
"This is the first blinded trial or sham controlled trial in the field of renal denervation," said Deepak Bhatt, professor of medicine at Harvard Medical School, and co-principal investigator.
The company that owns the technology, Medtronic, first announced in January that findings from Bhatt's study, called SYMPLICITY HTN-3, had shown the product to be ineffective and said it would halt enrollment in studies using it in Japan, India and the United States.
Medtronic bought the technology, known as the Symplicity Catheter System, in 2011 for $800 million dollars when it acquired the California-based company Ardian, Inc.
Franz H Messerli, director of the hypertension program at Mount Sinai hospital in New York, said this finding could spell the end for renal denervation, even though it contradicts most previous research on the therapy.
