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Eisenmenger SyndromeNCT02119442

Transcatheter Valve Implantation in Patients With Dysfunctional Left and Right Sided Heart Valves

A study testing Transcather Valve Implantation in people with Eisenmenger Syndrome, run by University of California, Los Angeles at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A growing body of data, suggests that transcatheter valves are effective when implanted in other locations (mitral, aortic, tricuspid) and in high pressure environments. The investigators plan to offer transcatheter valve implantation as an alternative to high risk surgery in patients who require revision of a… Read more about this study

Who is it for?
Any age
Conditions the study is for
Eisenmenger Syndrome
What is being tested?
Transcather Valve Implantation
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
1 siteUnited States
Study dates
Aug 2013to Feb 2018
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

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 Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Patients will be considered eligible for transcatheter valve implantation if the risk of serious morbidity or mortality with surgical intervention is deemed to be greater than 10 percent by the treating cardiologist and consulting surgeon. The Melody Valve is intended for use in the following clinical conditions:
  • Existence of a full (circumferential) RVOT conduit that was equal to or greater than 16 mm in diameter when originally implanted, AND
  • Dysfunctional RVOT conduits with a clinical indication for intervention, AND EITHER
  • Regurgitation ≥ moderate
  • Stenosis: mean right ventricular outflow tract gradient ≥ 35 mmHg
  • The Edwards Sapien Valve will be used in the aortic position for valves and conduits larger than 23mm in diameter with a landing zone less than 26-27mm, otherwise the melody valve will be considered
  • The Edwards Sapien Vavle will also be considered in other positions that have an adequate landing zone and a large enough circumference
  • The Melody valve may be utilized outside of its approved indications for valve replacement in high risk surgical patients

Who cannot join

  • There are no known contraindications for implantation of the Melody Valve or the Edwards Sapien Valve

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of California Los Angeles

    Los Angeles, California, 90095

Other trials in United States

About this study

A growing body of data, suggests that transcatheter valves are effective when implanted in other locations (mitral, aortic, tricuspid) and in high pressure environments. The investigators plan to offer transcatheter valve implantation as an alternative to high risk surgery in patients who require revision of a stenotic or regurgitant valve in the non-pulmonary position (mitral, aortic, tricuspid). This therapy can provide an alternative to patients who may be considered high risk and may not be able to survive a surgical procedure.The use of the devices on this protocol are for medical treatment and are not part of a clinical trial.

Read the detailed description

Many forms of congenital and structural heart disease require surgical placement of prosthetic valves and conduits. These conditions include many common congenital heart abnormalities such as Tetralogy of Fallot, Double Outlet Right Ventricle, Truncus Arteriosus and patients who require the Ross procedure for aortic stenosis. There are a variety of acquired conditions, including calcific aortic valve stenosis that may require surgical or transcatheter valve treatment. Unfortunately, when valved conduits are placed surgically, they ultimately become narrowed or regurgitant and require periodic replacement. Thus, patients with these conditions often undergo multiple open heart surgeries during their lifetime. Although the risk of mortality with this kind of surgery is low, surgical intervention is associated with significantly longer recovery times and more patient discomfort when compared to transcatheter interventions. Over the last decade, techniques have been developed to palliate these forms of congenital and structural heart disease using catheters inserted through blood vessels in the groin. These transcatheter techniques have allowed patients to delay or avoid open heart surgery.

The Medtronic Melody Trancatheter Valve and the Edwards SAPIEN Transcatheter Heart Valve are both bioprosthetic valves mounted within metal stents. Their entire structure is collapsible, allowing it to be inserted through delivery sheaths and threaded into the heart, typically without the need of surgical cardiopulmonary bypass. Some of these procedures may be performed using a hybrid technique of minimal surgical access and transcatheter valve delivery. The valves can then be expanded into place by inflating a balloon (similar to how stents are placed elsewhere in the heart, like the coronary artery). The Melody Valve received a humanitarian device exemption (HDE) from the FDA and the Edwards Sapien Valve has market approval from the FDA.The investigators plan to offer these transcatheter valves as alternatives to eligible patients who require replacement of a stenotic or regurgitant valve in all left and right sided positions.

The intended role of the Melody Transcatheter Pulmonary Valve is to restore pulmonary valve function in patients with a dysfunctional RVOT conduit and a clinical indication for pulmonary valve replacement. Unlike currently available options for pulmonary valve replacement, the TPV is intended to be placed with a transcatheter delivery system, and thus does not require surgical incisions, open heart surgery, cardiopulmonary bypass, or the various morbidities associated with surgical pulmonary valve replacement. The Edwards Sapien Valve is delivered in the same manner, but was intended for use in the aortic position. The ultimate goals and durability of the TPV may differ among patients with different indications. At a minimum, the intention is that the TPV will improve hemodynamic function, mitigate the adverse impact of valve regurgitation and/or obstruction, and effectively extend the longevity of the existing conduit and defer or obviate the need for conduit replacement. These techniques may decrease the number of open heart surgeries required over the course of a patient's lifetime, thereby decreasing the cumulative morbidity and risk associated with such operations.

With regards to valve replacement in any position with an adequate landing zone, the Melody Valve and Edwards Sapien Valve are presently being utilized at multiple United States centers for valve replacement in all positions in patients who are considered high risk candidates for surgical valve replacement. A recent article published by Zahn et al reported an experience in tricuspid valve implantations at three United States centers and one Austrailian center. Procedural success was achieved in all patients. Tricuspid regurgitation was reduced to mild or none in all patients. Noted complications were consistent with known risks of cardiac catheterization and Melody Valve implantation, regardless of indication. Similarly, an article published by Kenny et al demonstrated the successful implantation of the Sapien valve in the tricuspid position. Gillespie et al, recently published a series of Melody implants in the mitral position in sheep that had undergone annuloplasty ring placement. Other investigators have successfully implanted the Melody valve in the aortic and mitral positions in patients with good immediate and short/intermediate term outcomes (Ben-Gal et al, Hasan et al, Gossl et al). The Edwards Sapien Valve has several reports of positive outcomes when implanted within the aortic position (Thomas et al, Moat et al, Webb et al) and two case series that report encouraging results when placed in the mitral position. (Seiffert et al, Cheung et al)

Being tested
Transcather Valve Implantation
Keywords
Eisenmenger Syndrome, Pulmonary Arterial Hyptertension
Medical subject headings
Eisenmenger Complex

What participants receive

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

  • Transcather Valve ImplantationDevice

    Also called Medtronic Melody Transcatheter Valve; Melody TPV 20 PB1016:Melody TPV 22 PB1018, Edwards SAPIEN Transcatheter Heart Valve

    Transcather Valve Implantation

Study groups in NCT02119442
Study groupRoleWhat they receive
Transcatheter Valve ImplantationOtherIntervention, Transcatheter Valve Implantation with Melody or Sapien bioprosthetic valve Standard of care intervention.
Receives: Device: Transcather Valve Implantation

What is being measured

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

  1. Number of Participants Who Developed Infective Endocarditis

    The investigator will be assessing the efficacy of transcatheter heart valve (THV) by evaluating survival and development of infective endocarditis as an adverse event.

    Measured: 8 years

Timeline

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

  1. First posted21 Apr 2014 (estimated)
  2. Study startAug 2013
  3. Primary completionFeb 2018
  4. Study completionFeb 2018

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
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
90 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02119442
Sponsor's protocol ID
13-001008
Status last verified
Apr 2019
First submitted
8 Apr 2014
Last updated
30 Apr 2019
Data monitoring committee
No

Publications

  • Kondo N, Shuto T, McGarvey JR, Koomalsingh KJ, Takebe M, Gorman RC, Gorman JH 3rd, Gillespie MJ. Melody valve-in-ring procedure for mitral valve replacement: feasibility in four annuloplasty types. Ann Thorac Surg. 2012 Mar;93(3):783-8. doi: 10.1016/j.athoracsur.2011.12.021.

    PubMed 22364973
  • Riede FT, Dahnert I. Implantation of a Melody valve in tricuspid position. Catheter Cardiovasc Interv. 2012 Sep 1;80(3):474-6. doi: 10.1002/ccd.23404. Epub 2012 Mar 14.

    PubMed 22105855
  • Ben-Gal Y, Finkelstein A, Bruckheimer E, Banai S, Keren G, Kramer A, Uretzky G. Transapical implantation of a Melody valve in a degenerated low-diameter prosthetic aortic valve. Circulation. 2013 Apr 23;127(16):e553-6. doi: 10.1161/CIRCULATIONAHA.112.127027. No abstract available.

    PubMed 23609553
  • Cheung AW, Gurvitch R, Ye J, Wood D, Lichtenstein SV, Thompson C, Webb JG. Transcatheter transapical mitral valve-in-valve implantations for a failed bioprosthesis: a case series. J Thorac Cardiovasc Surg. 2011 Mar;141(3):711-5. doi: 10.1016/j.jtcvs.2010.11.026. Epub 2011 Jan 26.

    PubMed 21269643
  • Kenny D, Hijazi ZM, Walsh KP. Transcatheter tricuspid valve replacement with the Edwards SAPIEN valve. Catheter Cardiovasc Interv. 2011 Aug 1;78(2):267-70. doi: 10.1002/ccd.23016. Epub 2011 Jul 15.

    PubMed 21766424

Questions about this trial

What is this clinical trial studying?

A study testing Transcather Valve Implantation in people with Eisenmenger Syndrome, run by University of California, Los Angeles at 1 site in United States.

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 8 inclusion and 1 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: finished, as of the sponsor's last update on 30 Apr 2019. 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 United States. 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?

Yes. Results are posted in the registry (first posted 30 Apr 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants Who Developed Infective Endocarditis (time frame: 8 years). 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 NCT02119442, which also lists 5 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 30 Apr 2019.

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