The Nordic Aortic Valve Intervention Trial (NOTION)

• ClinicalTrials.gov Identifier: NCT01057173
• Recruitment Status: Active, not recruiting
• First Posted: January 27, 2010
• Last Update Posted: October 26, 2022
• Sponsor: Rigshospitalet, Denmark
• Collaborators: Odense University Hospital; Sahlgrenska University Hospital, Sweden; Danish Heart Foundation; Copenhagen Trial Unit, Center for Clinical Intervention Research
• Information provided by (Responsible Party): Hans Gustav Hørsted Thyregod, Rigshospitalet, Denmark

Study Description

Brief Summary:

A randomized clinical trial of transcatheter aortic valve implantation (TAVI) versus conventional surgical aortic valve replacement (SAVR) in patients older than 70 years of age suffering from severe aortic valve stenosis.

Study hypothesis: TAVI will reduce post-interventional morbidity and mortality compared to SAVR.

Condition or disease	Intervention/treatment	Phase
Critical Aortic Stenosis	Procedure: Transcatheter Aortic Valve Implantation; Procedure: Surgical Aortic Valve Replacement	Not Applicable

Detailed Description:

BACKGROUND: Transcatheter aortic valve implantation (TAVI) is a new and rapidly evolving treatment option for patients with severe degenerative aortic valve stenosis. Short- and mid-term results with transcatheter valve prostheses are promising in high-risk surgical patients, but long-term results are lacking. TAVI could potentially be an attractive minimally invasive treatment also for patients with moderate and low surgical risk, but no comparison has been made with the standard surgical treatment for aortic valve stenosis.

AIM: To compare TAVI and surgical aortic valve replacement (SAVR) in patients with severe aortic valve stenosis.

POPULATION: All patients with severe degenerative aortic valve stenosis referred for elective or subacute aortic valve intervention will be screened for study eligibility. To be included subjects must be 70 years or older, anatomical and technical eligible for both interventions, expected to survive more than 1 year after the intervention, and able to provide written informed consent. Study exclusion criteria include isolated aortic valve regurgitation or other significant valve disease, coronary artery disease requiring revascularisation at the time of referral, previous open heart surgery, a myocardial infarction or percutaneous coronary intervention within the last year, a cerebral infarction within the previous 30 days, severe renal -, pulmonary -, or infectious disease, and unstable preoperative condition.

DESIGN: The project is a national multicenter randomized clinical trial. Patients fulfilling all inclusion- and no exclusion criteria will be randomized to either TAVI or SAVR. Randomization will be 1:1 with 140 subjects in each group and stratified according to centre, age (70-74 years vs 75 and older), and coronary co-morbidity not requiring revascularisation (yes vs no). Primary outcome will be assessed by a blinded adjudication committee. Patients screened but not included in the study will be followed yearly. Screening and inclusion will commence in December 2009. Inclusion is expected to last 2 to 3 years, and subjects will be followed for 10 years.

INTERVENTIONS: Subjects randomized to TAVI will undergo percutaneous retrograde trans-femoral or trans-subclavian aortic valve implantation with the Medtronic CoreValve(TM) self-expandable bio-prosthesis. Before implantation a balloon dilatation of the aortic annulus will be performed. Subjects randomized to SAVR will undergo conventional surgical aortic valve replacement with a bio-prosthesis on cardiopulmonary bypass in normothermia with cold cardioplegia cardiac arrest. All interventions will be performed under general anaesthesia, and post-interventional medical and anticoagulation treatment will be uniform.

END POINTS: The primary end point is a combined outcome measure consisting of death from any cause, myocardial infarction, and stroke one year after the intervention. Secondary end points are death from any cause, cardiac death, cardiac -, cerebral -, pulmonary -, and renal complications, prosthesis re-intervention, procedure success and - time, admission lengths, functional class, quality of life, prosthesis and left ventricular structure and function. Follow-up visits will be performed after 30 days, 3, 6 and 12 months, and yearly thereafter for a minimum of 10 years.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 280 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: Transcatheter Versus Surgical Aortic Valve Implantation in Patients With Severe Aortic Valve Stenosis
• Actual Study Start Date: December 2009
• Actual Primary Completion Date: April 2014
• Estimated Study Completion Date: April 2033

Arms and Interventions

Arm	Intervention/treatment
Experimental: Transcatheter Aortic Valve Implantation	Procedure: Transcatheter Aortic Valve Implantation; Retrograde trans-femoral or trans-subclavian aortic valve implantation with the Medtronic CoreValve System(TM) bio-prosthesis (third generation system, 18 Fr, CE mark approved); Other Name: TAVI
Active Comparator: Surgical Aortic Valve Replacement	Procedure: Surgical Aortic Valve Replacement; Conventional surgical aortic valve replacement with a bio-prosthesis using normothermic cardiopulmonary bypass and cold blood cardioplegia cardiac arrest; Other Name: SAVR

Outcome Measures

Primary Outcome Measures :

1. Combined rate of death from any cause, myocardial infarction, and stroke [ Time Frame: 1 year ]
   Outcome measures will be defined as suggested by the Valvular Academic Research Consortium (VARC)

Secondary Outcome Measures :

1. Procedural complications [ Time Frame: Within first 30 days ]
2. Admission lengths (ICU and interventional center) [ Time Frame: Within first 30 days ]
3. Combined rate of noncardiac and cardiac death, prosthesis reintervention, cardiac-, cerebral-, renal-, and pulmonary complications [ Time Frame: 1 year ]
4. Functional status (NYHA-classification) and Quality of Life (SF-36) [ Time Frame: 1 year ]
5. Echocardiographic prosthesis and ventricular structural and functional status [ Time Frame: 1 year ]

Eligibility Criteria

• Ages Eligible for Study: 70 Years and older (Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Patients must have severe degenerative aortic valve stenosis (echocardiographic criteria: AV effective orifice area (EOA) of < 1 cm2, mean AV gradient of > 40 mmHg, or AV peak systolic velocity of > 4.0 m/s)
• Patients must be symptomatic from the aortic valve stenosis (dyspnoea in NYHA-class II or greater, angina pectoris, or syncope), or asymptomatic but with echocardiographic evidence of left ventricular hypertrophy, decreased left ventricular ejection fraction, or atrial fibrillation)
• Patients must be 70 years or older
• Patients must be technical and anatomical eligible for both interventions (as specified by Medtronic CoreValve(TM) for the TAVI procedure) after a formal consult by a cardiologist and a cardiovascular surgeon
• Patients must be expected to survive more than one year after the intervention
• Patients must be able to provide written informed consent as approved by the regional ethical committee after having received adequate information about the study
• Patients must be able and agree to return to all post-procedural follow-up visits

Exclusion Criteria:

• Isolated aortic valve insufficiency
• Other significant heart valve disease requiring intervention
• Coronary artery co-morbidity requiring revascularisation
• Any previous open heart surgery
• Myocardial infarction or percutaneous coronary intervention within the last year
• Stroke or TIA within the last 30 days
• Renal insufficiency requiring hemodialysis
• Pulmonary insufficiency (FEV1 or diffusion capacity < 40% of expected)
• Active infectious disease requiring antibiotics
• Emergency intervention (within 24 hours after the indication for intervention has been made)
• Unstable pre-interventional condition requiring inotropic support or mechanical heart assistance
• A known hypersensitivity or contraindication to heparin or nitinol
• Currently participating in an investigational drug or another device study

Contacts and Locations

Locations

Denmark

Copenhagen University Hospital

Copenhagen, Denmark, 2100

Odense University Hospital

Odense, Denmark, 5000

Sweden

Sahlgrenska University Hospital

Gothenburg, Sweden, 413 45

Sponsors and Collaborators

Rigshospitalet, Denmark

Odense University Hospital

Sahlgrenska University Hospital, Sweden

Danish Heart Foundation

Copenhagen Trial Unit, Center for Clinical Intervention Research

Investigators

• Principal Investigator: Hans GH Thyregod, MD, PhD; Dep. of Cardiothoracic Surgery, Rigshospitalet, Copenhagen University Hospital
• Principal Investigator: Lars Søndergaard, MD, DMSc; Dep. of Cardiology, Rigshospitalet, Copenhagen University Hospital

More Information

Publications of Results:

Thyregod HG, Steinbruchel DA, Ihlemann N, Nissen H, Kjeldsen BJ, Petursson P, Chang Y, Franzen OW, Engstrom T, Clemmensen P, Hansen PB, Andersen LW, Olsen PS, Sondergaard L. Transcatheter Versus Surgical Aortic Valve Replacement in Patients With Severe Aortic Valve Stenosis: 1-Year Results From the All-Comers NOTION Randomized Clinical Trial. J Am Coll Cardiol. 2015 May 26;65(20):2184-94. doi: 10.1016/j.jacc.2015.03.014. Epub 2015 Mar 15.

Thyregod HG, Steinbruchel DA, Ihlemann N, Ngo TA, Nissen H, Kjeldsen BJ, Chang Y, Hansen PB, Olsen PS, Sondergaard L. No clinical effect of prosthesis-patient mismatch after transcatheter versus surgical aortic valve replacement in intermediate- and low-risk patients with severe aortic valve stenosis at mid-term follow-up: an analysis from the NOTION trial. Eur J Cardiothorac Surg. 2016 Oct;50(4):721-728. doi: 10.1093/ejcts/ezw095. Epub 2016 Mar 22.

Sondergaard L, Steinbruchel DA, Ihlemann N, Nissen H, Kjeldsen BJ, Petursson P, Ngo AT, Olsen NT, Chang Y, Franzen OW, Engstrom T, Clemmensen P, Olsen PS, Thyregod HG. Two-Year Outcomes in Patients With Severe Aortic Valve Stenosis Randomized to Transcatheter Versus Surgical Aortic Valve Replacement: The All-Comers Nordic Aortic Valve Intervention Randomized Clinical Trial. Circ Cardiovasc Interv. 2016 Jun;9(6):e003665. doi: 10.1161/CIRCINTERVENTIONS.115.003665.

Ngo A, Hassager C, Thyregod HGH, Sondergaard L, Olsen PS, Steinbruchel D, Hansen PB, Kjaergaard J, Winther-Jensen M, Ihlemann N. Differences in left ventricular remodelling in patients with aortic stenosis treated with transcatheter aortic valve replacement with corevalve prostheses compared to surgery with porcine or bovine biological prostheses. Eur Heart J Cardiovasc Imaging. 2018 Jan 1;19(1):39-46. doi: 10.1093/ehjci/jew321.

Gronlykke L, Ihlemann N, Ngo AT, Thyregod HG, Kjaergaard J, Korshin A, Gustafsson F, Hassager C, Nilsson JC, Sondergaard L, Ravn HB. Measures of right ventricular function after transcatheter versus surgical aortic valve replacement. Interact Cardiovasc Thorac Surg. 2017 Feb 1;24(2):181-187. doi: 10.1093/icvts/ivw350.

Jorgensen TH, Thyregod HG, Tarp JB, Svendsen JH, Sondergaard L. Temporal changes of new-onset atrial fibrillation in patients randomized to surgical or transcatheter aortic valve replacement. Int J Cardiol. 2017 May 1;234:16-21. doi: 10.1016/j.ijcard.2017.02.098. Epub 2017 Feb 24.

Thyregod HGH, Ihlemann N, Jorgensen TH, Nissen H, Kjeldsen BJ, Petursson P, Chang Y, Franzen OW, Engstrom T, Clemmensen P, Hansen PB, Andersen LW, Steinbruchel DA, Olsen PS, Sondergaard L. Five-Year Clinical and Echocardiographic Outcomes from the Nordic Aortic Valve Intervention (NOTION) Randomized Clinical Trial in Lower Surgical Risk Patients. Circulation. 2019 Feb 1. doi: 10.1161/CIRCULATIONAHA.118.036606. Online ahead of print.

Sondergaard L, Ihlemann N, Capodanno D, Jorgensen TH, Nissen H, Kjeldsen BJ, Chang Y, Steinbruchel DA, Olsen PS, Petronio AS, Thyregod HGH. Durability of Transcatheter and Surgical Bioprosthetic Aortic Valves in Patients at Lower Surgical Risk. J Am Coll Cardiol. 2019 Feb 12;73(5):546-553. doi: 10.1016/j.jacc.2018.10.083.

Geisler BP, Jorgensen TH, Thyregod HGH, Pietzsch JB, Sondergaard L. Cost-effectiveness of transcatheter versus surgical aortic valve replacement in patients at lower surgical risk: results from the NOTION trial. EuroIntervention. 2019 Dec 6;15(11):e959-e967. doi: 10.4244/EIJ-D-18-00847.

Jorgensen TH, Thyregod HGH, Ihlemann N, Nissen H, Petursson P, Kjeldsen BJ, Steinbruchel DA, Olsen PS, Sondergaard L. Eight-year outcomes for patients with aortic valve stenosis at low surgical risk randomized to transcatheter vs. surgical aortic valve replacement. Eur Heart J. 2021 Aug 7;42(30):2912-2919. doi: 10.1093/eurheartj/ehab375.

Other Publications:

Thyregod HG, Sondergaard L, Ihlemann N, Franzen O, Andersen LW, Hansen PB, Olsen PS, Nissen H, Winkel P, Gluud C, Steinbruchel DA. The Nordic aortic valve intervention (NOTION) trial comparing transcatheter versus surgical valve implantation: study protocol for a randomised controlled trial. Trials. 2013 Jan 9;14:11. doi: 10.1186/1745-6215-14-11.

• Responsible Party: Hans Gustav Hørsted Thyregod, MD, PhD, Rigshospitalet, Denmark
• ClinicalTrials.gov Identifier: NCT01057173
• Other Study ID Numbers: HA2009046
• First Posted: January 27, 2010
• Last Update Posted: October 26, 2022
• Last Verified: October 2022

Keywords provided by Hans Gustav Hørsted Thyregod, Rigshospitalet, Denmark:

Heart Valve Disease; Heart Valve Prosthesis; Heart Valve Prosthesis Implantation; Randomized Controlled Trial

Additional relevant MeSH terms:

Aortic Valve Stenosis; Constriction, Pathologic; Pathological Conditions, Anatomical; Aortic Valve Disease; Heart Valve Diseases; Heart Diseases; Cardiovascular Diseases; Ventricular Outflow Obstruction