NETT Sends Mostly Positive Message for Controversial Lung Procedure

The mystery is over; the results of the National Emphysema Treatment Trial Research Group (NETT) have been unveiled, and it's by and large good news for device companies in interventional pulmonology. Although the outcomes are mixed and underscore the need for proper patient selection, clinicians are now hoping that clinical benefits demonstrated by NETT, a 1218-patient, five-year randomized prospective clinical trial comparing lung volume reduction surgery to medical management, will support reimbursement for the surgery.

The mystery is over; results of the National Emphysema Treatment Trial Research Group (NETT) have been unveiled and indicate that lung volume reduction surgery (LVRS) is beneficial for some emphysema patients who have no alternatives. Although the study had mixed outcomes, which underscore the need for proper patient selection for the procedure, advocates are hoping that its clinical benefits will be enough to convince the Centers for Medicare and Medicaid Services (CMS) to reimburse for the surgery.

Device companies in interventional pulmonology like Spiration Inc. , Broncus Technologies Inc. , Emphasys Medical, and Closure Medical...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Clinical Trials

Relief Cardiovascular Brings Relief To Heart Failure Patients With Smart Transcatheter Implant

 

Successful implantations of a novel transcatheter mark a major step forward in treating congestion in heart failure, according to the California -based company that developed it. The procedure was part of a feasibility study evaluating the device’s safety.

‘Much-Needed Tool For Large Tissue Biopsy’: Resitu Medical’s Breast Device FDA Authorized

 

Resitu Medical has received FDA 510(k) authorization for the RESL09 breast cancer biopsy device. This handheld minimally invasive device excises tissue samples with diameters up to 9 mm and will first reach market in the US. The company plans to expand the tool’s clinical claims and core size range.

Rapid Nexus Bets On Regeneration To Heal Wounds, Stop Amputations, Starting In VA Health Systems

 
• By 

Rapid Nexus hopes its regenerative wound-healing system can ease the burden of diabetic foot ulcers and amputations. Backed by early clinical data and $3.8m in seed funding, the start-up is targeting the VA as a launchpad into a $6.5bn US market, with FDA clearance expected later this year.

MCED Act Advances In US House Committees, Exact Sciences Cancerguard Poised To Benefit

 

The Nancy Gardner Sewell MCED Act has advanced in the US House, potentially allowing Medicare coverage for multi-cancer early detection tests. Exact Sciences is targeting FDA approval for its MCED test Cancerguard, launched in the US earlier this month.

More from R&D

Sava Technologies Microsensing Milestone: 10 Days Continuous Wear, No Finger-Prick Calibration

 

Sava Technologies has developed a CGM that uses microneedles to accurately measure glucose levels for up to 10 days without finger-prick calibration. The company raised £14.2m in Series A funding to establish in-house manufacturing for faster production.

INBRAIN, Mayo Clinic To Test BCI With Standard Deep Brain Stimulation In Parkinson’s Patients

 
• By 

Barcelona-based INBRAIN Neuroelectronics is partnering with Mayo Clinic to test whether its graphene-based cortical brain computer interface can enhance standard DBS in Parkinson’s, aiming for more precise adaptive therapy and improved gait outcomes.

New Guidelines Support Early Intervention With Edwards TAVR Device Sapien

 

The new ESC and EACTS guidelines allow aortic stenosis patients without symptoms to be considered for a transcatheter aortic valve replacement. The move opens the market for Edwards Lifesciences, the only medtech with a Europe and US-approved device for asymptomatic severe aortic stenosis.