St. Jude Medical Inc. has launched the U.S. clinical trial of its leadless pacemaker, the Nanostim, as it aims to win regulatory approval.
The device is less than 10 percent the size of a conventional pacemaker. Unlike other pacemakers, it does not have wires — called leads — that snake into the heart. Instead, the tiny pacemaker is implanted directly into the heart itself.
Nanostim is for patients who need "single-chamber pacing" — that is, only a single ventricle needs its rhythm sped up. But Dr. Mark Carlson, chief medical officer for St. Jude, said the goal is to expand the capabilities of such a tiny technology.
"We are certainly interested in bringing leadless technology to the full spectrum of pacing for patients," he said in an interview. "This is the initial endeavor. This is the logical and good place to start."
St. Jude's Leadless II trial is designed to evaluate the Nanostim for U.S. Food and Drug Administration approval. Its first use in the United States was at Mount Sinai Hospital in New York by Dr. Vivek Reddy.
St. Jude has had its share of issues with leads. In 2010, it pulled its Riata defibrillator lead from the U.S. market because of problems with inner wires coming through outer insulation. Its QuickSite and QuickFlex pacemaker leads also were pulled for the same reasons.
Besides avoiding design flaws with leads, St. Jude said the new device will reduce complications and improve patient comfort. Cardiologists must create a "pocket" just beneath the skin of the patient's chest to hold a traditional pacemaker generator. Doctors can implant Nanostim without such surgery, inserting it into the heart with a catheter that is steered up through a vein in the leg.
St. Jude said the Nanostim is fully retrievable, meaning that it can be repositioned during the implant procedure and later removed from the heart if necessary.