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Aortic Stenosis Treated With TAVINCT07059728

High Flow Nasal Oxygenation in Transcatheter Aortic Valve Replacement Procedures. TAVR-Highflow II

A study testing Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2) and Oxygen therapy during sedation delivered via nasal cannulae at 5L/min in people with Aortic Stenosis Treated With TAVI and Sedation; Aged; Hemodynamics, run by Hospital Clinic of Barcelona at 1 site in Spain.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Transcatheter aortic valve replacement (TAVR) has revolutionized the treatment of patients with aortic valve disease. TAVR is a less invasive treatment compared to the conventional surgical approach through median sternotomy. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2) and Oxygen therapy during sedation delivered via nasal cannulae at 5L/min
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
452 participants
Where
1 siteSpain
Study dates
1 Jan 2027to Dec 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Transfemoral TAVR elective procedure
  • Age >18 years

Who cannot join

  • Patients under 18 years of age
  • Refusal to participate
  • Known allergy to propofol or remifentanil.
  • Non-femoral surgical access.
  • Presence of a basal skull fracture or pneumothorax
  • Procedure duration < 45 minutes
  • Previously planned general anaesthesia approach due to patient's condition or procedural technical reasons
  • Need to convert to general anesthesia for non-respiratory complications within 45 minutes.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Spain1 site
  • Hospital Clinic de Barcelona

    Barcelona, Barcelona, 08036

    Antoni Manzano, Medecine, +34 618449998, anmanzano@clinic.cat

Other trials in Spain

About this study

Official title: Uso de Lentillas de Alto Flujo en Procedimientos de sustitución de válvula aórtica transcatéter. Impacto en Las Complicaciones Respiratorias y Biomarcado- Res y Resultados clínicos. TAVR-Highflow

Transcatheter aortic valve replacement (TAVR) has revolutionized the treatment of patients with aortic valve disease. TAVR is a less invasive treatment compared to the conventional surgical approach through median sternotomy.

Patients selected for this procedure often have a profile associated with multiple comorbidities which predispose them to certain complications.

Read more

TAVI procedures were initially performed under general anesthesia. However, due to improved procedure times and anesthetic techniques, sedation has become the current trend to preform them.

When sedation for these procedures requires deep planes, hypoxia is more likely to occur due to respiratory depression, apnea, or airway obstruction. This is even more common in TAVR patients population, as obesity, sleep apnea, elevated ASA classification, advanced age, and combined cardiorespiratory disease are highly prevalent.

For all these reasons, TAVR constitutes a risky procedure, presenting a profile of patients undergoing this procedure that can also be considered high risk.

The provision of supplemental oxygen through nasal cannulae or face masks can prevent the development of hypoxia. Unfortunately, non-humidified nasal oxygen cannot exceed 2-5 L/min without causing damage to the nasal mucosa, and the percentage of oxygen delivered through variable-flow face masks is unpredictable.

On the other hand, high-flow nasal oxygen therapy (HFNO) can provide humidified gas flow rates of up to 70 L/min through specially adapted nasal cannulae and reliably deliver oxygen concentrations between 21% and 100%. The use of HFNC could be justified in this context and could improve the outcomes and safety of these procedures, increasing oxygen content and minimizing hypercapnia.

The study's hypothesis is HFNO will prevent hypoxemia and control hypercapnia during sedation for transcatheter aortic valve implantation (TAVI) better than conventional oxygen theraphy. Clinical and serological biomarkers of tissue injury will decrease with the use of HFNO. Clinical complications will decrease with the use of HFNO.

The study population would be all patients >18 years of age undergoing TAVI procedure and who agree to participate in the study in 8 centers in Barcelona.

Read the detailed description

Transcatheter aortic valve replacement (TAVR) has revolutionized the treatment of patients with aortic valve disease. TAVR is a less invasive treatment compared to the conventional surgical approach through median sternotomy. These technological advances have enabled a minimally invasive anesthetic approach that avoids mechanical ventilation, central line insertion, and urinary catheterization in most patients undergoing TAVR.

However, patients selected for this procedure often have a profile associated with multiple comorbidities such as pulmonary disease, ischemic coronary artery disease, and atherosclerosis of the carotid and renal arteries, which predispose them to certain complications.

Acute kidney injury (4%-35%), ischemic stroke (1%-3%), acute heart failure (7%-24%), and hypoxemia with hypercapnia are the most common perioperative complications. The overall 30-day mortality rate is 2.2%.

Because they are considered high-risk (both due to the procedure and the type of patient undergoing this procedure) and due to their duration, TAVI procedures were initially performed under general anesthesia. With improved procedure times and improved anesthetic techniques, the trend is to attempt to perform these procedures under deep sedation. As in many settings, sedation for diagnostic and/or therapeutic procedures can be achieved with a variety of medications, the goal of which is sedation to enable procedural success. The development and advancement of procedures as an alternative to surgery and/or more invasive diagnostic and therapeutic procedures means that the use of less invasive techniques is becoming increasingly common. Depending on the procedure, sedation may be required. However, despite the less invasive nature of these tests, deep sedation is frequently required for these procedures.

Deep sedation techniques have developed alongside technological advances that enable the provision of complex diagnostic and therapeutic procedures, often performed in settings outside the operating room. These settings include procedure rooms, radiology departments, outpatient departments, emergency rooms, surgical facilities, interventional cardiology departments, and so on. Deep sedation is used to support and enable the performance of these procedures. Enthusiasm for providing sedation for these procedures in a non-OR setting was tempered by an increase in mortality in non-OR areas, even leading one author to describe this as the "Wild West" of surgical and anesthetic practice. This required both professionals and regulatory authorities have developed increased oversight to improve the quality of care for out-of-the-operative procedures.

When sedation for these procedures requires deep planes, hypoxia is more likely to occur due to respiratory depression, apnea, or airway obstruction. This is even more common in patients at risk due to obesity, sleep apnea, elevated ASA classification, age >60 years, and combined cardiorespiratory disease. The reported incidence of hypoxia ranges from 10% to 70%, depending on the definition of hypoxia used. The risk of hypoxia further increases with the duration of the procedure.

The risk of periprocedural hypoxia can be reduced by monitoring respiratory and sedation parameters. However, even the most effective monitoring and standards of care may not be sufficient to reverse the respiratory compromise caused by deep sedation. Deep sedation affects the respiratory system through effects on normal cardiorespiratory physiology. These changes include a drop in respiratory rate, tidal volume, and changes in cardiorespiratory dynamics, and these effects are further affected by patient positioning. Subjects with cardiorespiratory diseases, such as pulmonary hypertension and chronic respiratory diseases, are particularly at risk for a critical decline in function.

The provision of supplemental oxygen through nasal cannulae or face masks can prevent the development of hypoxia. Unfortunately, non-humidified nasal oxygen cannot exceed 2-5 L/min without causing damage to the nasal mucosa, and the percentage of oxygen delivered through variable-flow face masks is unpredictable.

High-flow nasal oxygen therapy (HFNO), which is also unique in that it is humidified, was developed to provide flow rates of up to 70 L/min through specially adapted nasal cannulae and reliably delivers oxygen concentrations between 21% and 100%. Many operators are finding that combining deep planes of sedation with HFNC reduces the risk of periprocedural hypoxia. HFNC reduces the work of breathing, physiological dead space and provides an element of positive end-expiratory airway pressure.

HFNO has the potential to reduce procedural hypoxic events, procedural interruptions, and increase therapeutic success. However, although not all trials have concluded that HFNO improves safety compared to standard nasal oxygen therapy, the experience of most operators is positive.

The additional cost of HFNO may be a limiting factor for its use during procedural sedation, but it may be justified in high-risk procedures and patients with risk factors (already discussed), as it improves safety and quality of care. Deep sedation now allows complex diagnostic and therapeutic procedures to be performed outside the operating room in high-risk patients, but it is not without risk, and tools must be developed to mitigate the possibility of such risk.

For all the reasons stated above, TAVI constitutes a risky procedure, presenting a profile of patients undergoing this procedure that can also be considered high risk. The use of HFNC could be justified in this context and could improve the outcomes and safety of these procedures.

The use of HFNC during sedation for TAVI could increase oxygen content and minimize hypercapnia, which frequently occur. This may have two potential benefits: one in terms of facilitating patient tolerance to anesthetic sedation; and the other in optimizing oxygen delivery to organs such as the brain, kidneys, and myocardium. Currently, the profile of patients typically proposed for TAVI is those with aortic disease and significant morbidity and/or older age, who have been ruled out for conventional surgery. These patients are more likely to develop periprocedural complications, being specially sensitive to them.

In a recent study conducted in the United Kingdom, the use of HFNO with a FiO2 of 30% was associated with an 18% reduction in desaturation episodes; however, a decrease in hypoxemia measured by arterial oxygen levels could not be observed.

In a recent randomized clinical trial conducted at the Hospital Clínic in Barcelona (currently under review), the use of HFNO with a FiO2 of 60% was associated with a 31% reduction in desaturation episodes, higher arterial oxygen levels, and improved postoperative renal function, both analytically (measured by creatinine and glomerular filtration rate) and clinically (a 10% reduction in the incidence of renal failure according to VARC criteria).

However, several questions remain to be determined. First, a potential impact (both clinical and analytical) on preventing damage to other target organs (brain and heart). Second, the identification of patient subgroups at higher risk of desaturation and hypoxemia during deep sedation and who, consequently, may benefit more from HFNC treatment. Finally, there is still no data to assess the clinical impact of HFNC on clinical variables such as mortality, hospital stay, and reduction of postoperative complications (stroke, delirium, heart failure, etc.).

The justification for the study would be the use of HFNC, a therapy already available in healthcare centers but not widely used for these procedures. The risks of its use are comparable to those of conventional nasal oxygen therapy. Potential benefits would include a reduction in respiratory complications, a potential improvement in organ-specific biomarker levels, and a potential reduction in clinical cardiological, neurological, and renal complications, as well as an improvement in hospital stay and periprocedural mortality.

The study population would be all patients >18 years of age undergoing TAVI procedure and who agree to participate in the study in 8 centers in Barcelona.

Being tested
Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2), Oxygen therapy during sedation delivered via nasal cannulae at 5L/min
Keywords
Aortic Stenosis, TAVR, Sedation
Medical subject headings
Aortic Valve Stenosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2)Device

    Intervention group: Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2)

  • Oxygen therapy during sedation delivered via nasal cannulae at 5L/minDevice

    Control group: Oxygen therapy during sedation delivered via nasal cannulae at 5L/min

Study groups in NCT07059728
Study groupRoleWhat they receive
HFNO groupExperimentalPatients recieving high flow nasal oxygenation
Receives: Device: Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2)
Control groupActive comparatorPatients recieving standard of care oxygen theraphy (5L/min via nasal cannulae)
Receives: Device: Oxygen therapy during sedation delivered via nasal cannulae at 5L/min

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postoperative complications

    Reduction in complications at 30 days post-procedure). Classic composite variable that includes: 30-day post-procedure mortality, need for hospital readmission due to acute heart failure, incidence of stroke, and incidence of acute kidney injury.

    Measured: From enrollment to 30 days after intervention

  2. Win ratio

    Win ratio analysis for outcomes: 30-day post-procedure mortality, need for hospital readmission for acute heart failure, incidence of acute stroke, incidence of acute kidney injury, and quality of life (measured by the Kansas Questionnaire)

    Measured: From enrollment to 30 days after the intervention ends

Secondary outcomes (12)
  1. Number of Desaturation episodes

    Pulse oximetry values inferior to 93% for a period of more than 10 seconds.

    Measured: From enrollment until end of TAVR procedure

  2. Desaturation incidence

    Probability of presenting at least 1 episode of desaturation

    Measured: From enrollment until the end of TAVR procedure

  3. PaO2

    Arterial partial pressure oxygen

    Measured: At enrollment and at 45 minutes after enrollment

  4. PaCO2

    CO2 arterial partial pressure

    Measured: At enrollment and at 45 minutes after enrollment.

  5. Neuronal Specific Enolase

    Serological Neuronal Specific Enolase levels.

    Measured: At enrollment and at 8 hours after enrollment.

  6. Creatinine

    Creatinine serological levels

    Measured: At enrollment and at 8 hours after enrollment.

  7. Troponin

    Ultra-sensitive Troponin serological levels

    Measured: At enrollment and at 8 hours after enrollment.

  8. NT-proBNP

    NT-proBNP serological levels

    Measured: At enrollment and at 8 hours after enrollment.

  9. Number of patients presenting with respiratory depression

    Any desaturation episode that leads to patient's manual ventilation from responsible anesthesiologyst in order to mantain patients well being.

    Measured: From enrollment until the end of TAVR procedure

  10. Vasopressors

    Drugs used to mantain mean blood pressure levels above 65mmHg. Drug used and dose administered.

    Measured: From enrollment until the end of TAVR procedure.

  11. Propofol and remifentanil

    Drugs used to induce and mantain hypnosis. Total amount of propofol and remifentanil administered during the procedure

    Measured: From enrollment until the end of TAVR procedure

  12. Procedural duration

    Time of duration of sedation

    Measured: Procedure (Time from start of sedation to when sedation drugs are stopped)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jul 2025
  2. Study start1 Jan 2027 (estimated)
  3. Primary completionJul 2028 (estimated)
  4. Study completionDec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
452 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07059728
Sponsor's protocol ID
HCB/2025/0514
Status last verified
Sep 2026
First submitted
18 Jun 2025
Last updated
18 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Scheuermann S, Tan A, Govender P, Mckie M, Pack J, Martinez G, Falter F, George S, A Klein A. High-flow nasal oxygen vs. standard oxygen therapy for patients undergoing transcatheter aortic valve replacement with conscious sedation: a randomised controlled trial. Perioper Med (Lond). 2023 Apr 14;12(1):11. doi: 10.1186/s13741-023-00300-8.

    PubMed 37060038
  • Turnbull D. High-flow nasal oxygen, procedural sedation, and clinical governance. Minerva Anestesiol. 2022 May;88(5):407-410. doi: 10.23736/S0375-9393.21.16078-X. Epub 2021 Sep 16.

    PubMed 34527411
  • Riddell Z, Pressler N, Siau K, Mulder CJJ, Shalmani HM, Downs A, Gait A, Ishaq S. Feasibility of high-flow nasal oxygen therapy and two-stage sedation during endoscopic hypopharyngeal therapy. JGH Open. 2020 May 16;4(4):743-748. doi: 10.1002/jgh3.12348. eCollection 2020 Aug.

    PubMed 32782965
  • Riccio CA, Sarmiento S, Minhajuddin A, Nasir D, Fox AA. High-flow versus standard nasal cannula in morbidly obese patients during colonoscopy: A prospective, randomized clinical trial. J Clin Anesth. 2019 May;54:19-24. doi: 10.1016/j.jclinane.2018.10.026. Epub 2018 Nov 2.

    PubMed 30391445
  • Kim SH, Bang S, Lee KY, Park SW, Park JY, Lee HS, Oh H, Oh YJ. Comparison of high flow nasal oxygen and conventional nasal cannula during gastrointestinal endoscopic sedation in the prone position: a randomized trial. Can J Anaesth. 2021 Apr;68(4):460-466. doi: 10.1007/s12630-020-01883-2. Epub 2021 Jan 6.

    PubMed 33403549
  • Sago T, Harano N, Chogyoji Y, Nunomaki M, Shiiba S, Watanabe S. A nasal high-flow system prevents hypoxia in dental patients under intravenous sedation. J Oral Maxillofac Surg. 2015 Jun;73(6):1058-64. doi: 10.1016/j.joms.2014.12.020. Epub 2014 Dec 30.

    PubMed 25799356
  • Lin Y, Zhang X, Li L, Wei M, Zhao B, Wang X, Pan Z, Tian J, Yu W, Su D. High-flow nasal cannula oxygen therapy and hypoxia during gastroscopy with propofol sedation: a randomized multicenter clinical trial. Gastrointest Endosc. 2019 Oct;90(4):591-601. doi: 10.1016/j.gie.2019.06.033. Epub 2019 Jul 3.

    PubMed 31278907
  • Teng WN, Ting CK, Wang YT, Hou MC, Chang WK, Tsou MY, Chiang H, Lin CL. High-Flow Nasal Cannula and Mandibular Advancement Bite Block Decrease Hypoxic Events during Sedative Esophagogastroduodenoscopy: A Randomized Clinical Trial. Biomed Res Int. 2019 Jul 16;2019:4206795. doi: 10.1155/2019/4206795. eCollection 2019.

    PubMed 31380421
  • Ischaki E, Pantazopoulos I, Zakynthinos S. Nasal high flow therapy: a novel treatment rather than a more expensive oxygen device. Eur Respir Rev. 2017 Aug 9;26(145):170028. doi: 10.1183/16000617.0028-2017. Print 2017 Sep 30.

    PubMed 28794144
  • Wen Z, Wang W, Zhang H, Wu C, Ding J, Shen M. Is humidified better than non-humidified low-flow oxygen therapy? A systematic review and meta-analysis. J Adv Nurs. 2017 Nov;73(11):2522-2533. doi: 10.1111/jan.13323. Epub 2017 May 30.

    PubMed 28440960
  • Wagstaff TA, Soni N. Performance of six types of oxygen delivery devices at varying respiratory rates. Anaesthesia. 2007 May;62(5):492-503. doi: 10.1111/j.1365-2044.2007.05026.x.

    PubMed 17448063
  • Raman V, Raman V, Tobias JD. Dexmedetomidine and Pulmonary Hype- rtension: A Case Report and Review of the Literature. J Med Cases. 2013;4(7):481-484. doi:10.4021/jmc.v4i7.1279

  • Wang CY, Ling LC, Cardosa MS, Wong AK, Wong NW. Hypoxia during upper gastrointestinal endoscopy with and without sedation and the effect of pre-oxygenation on oxygen saturation. Anaesthesia. 2000 Jul;55(7):654-8. doi: 10.1046/j.1365-2044.2000.01520.x.

    PubMed 10919420
  • Bell JK, Laasch HU, Wilbraham L, England RE, Morris JA, Martin DF. Bispectral index monitoring for conscious sedation in intervention: better, safer, faster. Clin Radiol. 2004 Dec;59(12):1106-13. doi: 10.1016/j.crad.2004.04.008.

    PubMed 15556593
  • Saunders R, Struys MMRF, Pollock RF, Mestek M, Lightdale JR. Patient safety during procedural sedation using capnography monitoring: a systematic review and meta-analysis. BMJ Open. 2017 Jun 30;7(6):e013402. doi: 10.1136/bmjopen-2016-013402.

    PubMed 28667196

Questions about this trial

What is this clinical trial studying?

A study testing Oxygen therapy during sedation provided via high nasal cannulae (60L/min at 60% FiO2) and Oxygen therapy during sedation delivered via nasal cannulae at 5L/min in people with Aortic Stenosis Treated With TAVI and Sedation; Aged; Hemodynamics, run by Hospital Clinic of Barcelona at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 18 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postoperative complications (time frame: From enrollment to 30 days after intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07059728, which also lists 27 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2026.

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