ClinicalTrials.gg
CompletedNCT02119442Updated Apr 30, 2019Results posted

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

An interventional study of Transcather Valve Implantation in Eisenmenger Syndrome, sponsored by University of California, Los Angeles. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2019-04-30.

Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Not applicable
Sex
All
01

Study 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 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)

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Conditions studied

  • Eisenmenger Syndrome

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Keywords

  • Eisenmenger Syndrome, Pulmonary Arterial Hyptertension
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In context

Eisenmenger Complex

23 studies on the registry are indexed under Eisenmenger Complex; 5 are open to participants now.

This study's enrollment of 90 is above the median of 40 across 15 interventional studies indexed under Eisenmenger Complex.

Browse Eisenmenger Complex studies →

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,170 studies on the registry; 195 are open to participants now.

Of its 95 completed or terminated interventional studies of FDA-regulated products, 70 (74%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • There are no known for implantation of the Melody Valve or the Edwards Sapien Valve
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
90 participants (actual)

Study arms

  • Other
    Transcatheter Valve Implantation

    Intervention, Transcatheter Valve Implantation with Melody or Sapien bioprosthetic valve Standard of care intervention.

    Device: Transcather Valve Implantation

Interventions

  • DeviceTranscather Valve Implantation

    Transcather Valve Implantation

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

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What researchers measure

Primary outcomes

  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.

    Time frame: 8 years

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Results

Posted Apr 30, 2019

Participant flow

Participant flow — Overall Study
MilestoneTranscatheter Valve Implantation
Started90
Completed90
Not completed0

Outcome measures

PrimaryNumber 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.

Time frame:
8 years
Reported as:
Number · participants
Number of Participants Who Developed Infective Endocarditis
participantsTranscatheter Valve Implantation
Number of Participants Who Developed Infective Endocarditis9

Adverse events

Collected over Adverse event data were collected until the latest follow up time point that the patients were seen by a physician. This time point included at least one year of follow up or more.. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Transcatheter Valve Implantation4/90 (4.4%)9/90 (10%)0/90 (0%)
Most frequent serious events
Most frequent serious events
EventTranscatheter Valve Implantation
infective endocarditisCardiac disorders9/90

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Transcatheter Valve Implantation
<=18 years25
Between 18 and 65 years62
>=65 years3
Age, Continuous
Age, Continuous(years)Transcatheter Valve Implantation
Mean25 (3 to 77)
Sex: Female, Male
Sex: Female, Male(Participants)Transcatheter Valve Implantation
Female44
Male46
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)Transcatheter Valve Implantation
Region of Enrollment
Region of Enrollment(participants)Transcatheter Valve Implantation
United States90
08

Study locations

1 site
  • University of California Los Angeles
    Los Angeles, California 90095, United States
09

References and documents

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 ↗

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02119442
Responsible party
Jamil Aboulhosn (Associate Professor of Clinical Medicine, University of California, Los Angeles) — Principal investigator
First posted
Apr 21, 2014
Start date
Aug 2013
Primary completion
Feb 2018
Completion
Feb 2018
Results posted
Apr 30, 2019
Last update
Apr 30, 2019

Study contacts

Jamil A Aboulhosn, MD, FACC
principal investigator · University of California, Los Angeles

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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