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Acute Myocardial InfarctionPhase 4OCTAVIANCT02577965

Optical Coherence Tomography Assessment of Gender diVersity In Primary Angioplasty: The OCTAVIA Trial

A Phase 4 study testing Percutaneous Coronary Intervention and XIENCE PRIME Everolimus Eluting Coronary Stent System in people with Acute Myocardial Infarction, run by A.O. Ospedale Papa Giovanni XXIII.

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

Recent studies suggest important gender differences in the pathophysiology and prognosis of ST-segment elevation myocardial infarction (STEMI). This is the first prospective controlled study to assess gender differences in the mechanism of plaque rupture/erosion and thrombus formation in patients presenting with STEMI… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Myocardial Infarction
What is being tested?
Percutaneous Coronary Intervention and XIENCE PRIME Everolimus Eluting Coronary Stent System
Could I receive a placebo?
No, everyone receives an active treatment
How many people
140 participants
Where
No sites listed yet
Study dates
Mar 2011to Sep 2014
Phase
Phase 4
Are there results?
None posted in the registry

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

  • Acute Myocardial MI with ST segment Elevation, within 6 hours from symptoms onset
  • Native coronary artery disease (no prior stent implant, no prior brachytherapy)
  • Signed patient informed consent

Who cannot join

  • Patients with left main disease
  • infarct lesions in bypass grafts
  • cardiogenic shock
  • renal failure
  • recent major bleeding
  • allergy to aspirin or clopidogrel
  • on anticoagulant therapy
  • no suitable anatomy for OCT (extreme tortuousity, very distal culprit lesion, and large infarct vessel > 4 mm in diameter)

About this study

Recent studies suggest important gender differences in the pathophysiology and prognosis of ST-segment elevation myocardial infarction (STEMI). This is the first prospective controlled study to assess gender differences in the mechanism of plaque rupture/erosion and thrombus formation in patients presenting with STEMI treated with primary angioplasty. Gender-related mechanisms of plaque rupture or erosion will be investigated using a combination of Quantitative Coronary Angiography (QCA), high resolution Optical Coherence Tomography (OCT) of the culprit vessel and histopathology analyses of thrombus aspirates of the infarct related lesion, performed by independent core laboratories, blinded to group (male or female) and clinical variables.

In OCTAVIA; enrollment in a 1:1 ratio according to gender group will be ensured by a computer-assisted matching algorithm for gender and age (< 50, 51-70, and > 70 years). Matching has the purpose to enable enrollment of an even number of male and female patients in balanced age groups. This type of dynamic algorithm is appropriate when the composition of the referral population is not known in advance.

The sample size for the OCTAVIA study was calculated on the basis of per patient stent strut coverage (a continuous variable with right skewed distribution) with mean of 97.0% and standard deviation of 4.0% in men, versus mean of 95.0% and standard deviation of 4.0% in women, following XIENCE PRIME™ Everolimus Eluting Coronary Stent System implantation. Thus, aiming for a 5% 2-tailed superiority alpha, an 80% power, and assuming a 1:1 enrollment according to gender, a total of 64 patients per group should be enrolled. Anticipating a 10% dropout rate due to patients lost to follow-up and inadequate imaging (included major side branch sections), the total enrollment is set at 70 patients per group (total population of 140 subjects).

Read the detailed description

A suboptimal degree of attention has focused on the detection and management of coronary artery disease (CAD) in women until recently. Although many women do not perceive heart disease as a significant health risk, CAD is the leading cause of mortality in women in most developed nations, with mortality primarily driven by acute ST-elevation myocardial infarction (STEMI) and cardiogenic shock (American Heart Association 2005 Heart Disease and Stroke Statistics).

In recent years, literature articles regarding various aspects of heart disease in women significantly increased. These reports have highlighted important sex differences in the pathophysiology, presentation, and treatment of ischemic heart disease and have denounced pervasive sex-related disparities in referral and treatment for heart disease as a major reason for outcome differences between the sexes. Such activities have been useful in driving attention to heart disease in women, an area largely ignored by the scientific community and the public just 20 years ago.

However, we must recognize that to date, limited data substantiate many of these statements; such recognition is important to guide future research efforts. A careful look at recently published literature reveals only modest advancements toward clarifying gender-based differences in the pathophysiology of ischemic heart disease and gender-based differences in outcome. At the same time, key questions concerning strategies for prevention and treatment of heart disease in women remain unanswered, and cardiovascular clinical trials continue to include fewer women than men.

A fundamental question is whether the mechanisms underlying ischemic heart disease in women differ from those in men. This is an important question because if pathophysiology differs in women, such differences can inform strategies for prevention, detection, and treatment that would be most effective for women.

A number of indicators point to a different mechanism in man and women.

  1. More symptoms, but less diseased vessels. Despite having more symptoms and physical limitations, women have less obstructive coronary heart disease than men, as assessed by angiography along the entire spectrum of acute coronary syndromes. Chest pain without apparently severe obstructive coronary artery disease (CAD) is distinctly more common in women than in men.
  2. Disability unrelated to severity of coronary obstructions. Among women, chest pain symptoms and disability do not correlate with severity of coronary stenosis, assessed by angiography.
  3. Higher risk after infarction despite lesser cardiac damage. Women, particularly those who are young or middle-aged (whom one would expect to be most advantaged for coronary disease risk compared with men due to estrogen protective actions), show higher rates of adverse outcomes after acute myocardial infarction (MI) than men of similar age, despite less severe coronary narrowing, smaller infarcts, and more preserved systolic function.

Consequently, the identification of less obstructive atheroma has been put forth as a potentially helpful strategy for the risk stratification of women.

Although this is a compelling theory, to date there is little evidence to suggest that vascular abnormalities in the absence of obstructive atheroma as detected by angiography are more commonly implicated in the pathogenesis of ischemia among women than men.

Recent studies have evaluated gender differences in coronary structure and function using intravascular ultrasound and other types of vascular testing. These studies have found that women had less atheroma volume than men, including both luminal plaque and atheroma within the media, despite older age and more risk factors, and even after accounting for body surface area and vessel size. After adjusting for body size, women also have smaller coronary vessels. However, these studies were unable to identify other vascular abnormalities, like plaque characteristics, that might explain gender differences in clinical presentation.

Presently, we are far from being able to conclude, or even suggest, that these hypothesized abnormalities play a larger etiologic or prognostic role for ischemic heart disease among women than among men.

A general pattern of higher mortality and complication rates in women after acute coronary syndromes (ACS) compared with men has been described for many years. It is important to recognize, however, that gender differences in mortality after ACS do not occur across the board but only in specific patient subgroups.

It is hypothesized that differences by MI type (STEMI versus other types) may be due to the pathophysiology underlying these events. For example, acute occlusion caused by thrombus superimposed on a ruptured or eroded atherosclerotic plaque is believed to play a larger role in trans mural infarctions than other types of ACS. Thus, it is possible that gender differences in vessel size and collateralization put women at greater risk than men after STEMI but not after other types of ACS.

It is also unclear why gender differences in the outcome of MI are seen in young and middle-aged patients but not older patients. One would expect that women younger than 50 years of age, the majority of whom are premenopausal, should be more advantaged rather than less advantaged compared with men of similar age in terms of survival. On the other hand, for coronary disease to occur in younger women, it must be aggressive, driven by multiple risk factors, or caused by secondary or unknown causes.

A less aggressive clinical treatment of women with coronary heart disease relative to men has been documented for years, with a tendency to refer to it as gender bias in health care delivery.

A 2005 Statement from the American Heart Association reviewed gender-specific data on the safety and efficacy of percutaneous coronary intervention and pharmacotherapy. Despite the fact that more women than men die from cardiovascular disease in the United States, and despite the established benefits of Percutaneous Coronary Intervention (PCI) in reducing fatal and nonfatal ischemic complications in patients with acute myocardial infarction, only an estimated 33% of annual PCIs are performed in women. In addition, women experience greater delays to intervention and are referred for diagnostic catheterization less frequently than are men.

Recent advances in angioplasty equipment and technique have improved options for patients with smaller coronary and peripheral (access) arteries. In addition, the increased use of stents and adjunctive pharmacotherapy has improved outcomes in both women and men. Nevertheless, women continue to represent 15% to 38% of the population in studies of PCI, and still relatively few gender- or race-specific data exist.

According to the American Heart Association, better understanding and elimination of this apparent treatment disparity is a priority. One of the areas of interest is to refine treatment pathways and strategies for women with STEMI, in whom mortality rates and bleeding risk remain higher than in men.

To further optimize clinical outcomes of women undergoing PCI, evidence-based evaluation in randomized clinical trials must emphasize increased recruitment of women, with mandates to include gender-specific, ethnic, and racial gender-based results.

Cardiovascular Optical Coherence Tomography (OCT) is an innovative catheter-based imaging technology that utilizes light rather than ultrasound to obtain unique details of the vessels on a microscopic scale. OCT provides high-resolution (10 to 15 micron axial), full tomographic in vivo images and measurements of coronary arteries and deployed stents with a high level of accuracy.(8,9) Applications of this technique include diagnostic assessments of coronary atherosclerosis and guidance of coronary interventions.

After at least a decade of renewed interest in women's cardiovascular health, we are left with more questions than answers. Fundamental questions about the pathophysiology of ischemic heart disease in women remain unanswered. We have gained few clues about the basis for gender differences in coronary heart disease and what is unique about the female vascular system. As a result, we are yet unable to explain gender differences in the epidemiology, presentation, treatment and outcome of coronary heart disease. Key questions remain about why women are protected from cardiovascular disease, why this protection is restricted to the coronary system, and why this protection ends when women have diabetes or an acute MI.

We lack studies that compare biological mechanisms of disease between women and men to better define vascular processes that are unique to women. We lack sufficiently large follow-up studies to link such processes to cardiac end points. How can we increase the inclusion of women in cardiovascular clinical trials? Without an answer to these questions, little can be done to improve the prevention and the treatment of coronary heart disease in women.

In STEMI patients, acute coronary occlusion caused by thrombus superimposed on a ruptured or eroded plaque plays an important role. Nevertheless, no evidence is available concerning the mechanism of plaque rupture, the underlying vascular abnormalities of the infarct related vessel and the biological responses such as vascular remodeling and repair, that are unique to women.

In the OCTAVIA trial, gender-related mechanisms of plaque rupture will be investigated using a combination of Quantitative Coronary Angiography (QCA), OCT and histopathology analyses of thrombus aspirates of the culprit lesion performed by independent core laboratories, blinded to the group assignment.

By combining clinical variables with QCA, OCT and thrombus analysis, it is possible to obtain critical information concerning the relationship between serological biomarker of cardiac damage, clinical and prognostic correlates of coronary plaque morphology and the underlying mechanisms of coronary thrombosis in women.

In addition to assessing gender differences in the mechanism of plaque rupture, OCTAVIA will also evaluate the changes in the vascular territory remote from the infarct related lesion, the local vascular response to primary angioplasty interventions and the correlation with clinical outcomes over one year of follow-up. These data are important to support a gender based differential strategy and can have a substantial impact for the improvement of clinical practice in the treatment of women with STEMI.

Being tested
Percutaneous Coronary Intervention, XIENCE PRIME Everolimus Eluting Coronary Stent System
Keywords
ST segment Elevation Myocardial Infarction, Optical Coherence Tomography, Percutaneous Coronary Intervention, Thrombus histopathology, Gender differences
Medical subject headings
ST Elevation Myocardial Infarction

What participants receive

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

  • Percutaneous Coronary InterventionProcedure or surgery

    Thrombus aspiration and histopathological analysis ,Optical Coherence Tomography assessment of culprit vessel during primary PCI, Primary PCI and Drug Eluting Stent (DES) - XIENCE PRIME Everolimus Eluting Coronary Stent implantation in culprit lesion, coronary angiography and OCT assessment at 9 months follow-up

  • XIENCE PRIME Everolimus Eluting Coronary Stent SystemDevice

    Xience Prime Everolimus Eluting Coronary Stent System implantation to treat Acute Myocardial Infarction

Study groups in NCT02577965
Study groupRoleWhat they receive
Female ArmExperimentalFemale gender diagnosed with ST segment Elevation Myocardial Infarction (STEMI). Interventions: Angiography, thrombus aspiration, optical coherence tomography and percutaneous coronary intervention, implantation of XIENCE PRIME Everolimus Eluting Coronary Stent. Angiography and Optical Coherence Tomography follow up at 9 months.
Receives: Procedure: Percutaneous Coronary Intervention; Device: XIENCE PRIME Everolimus Eluting Coronary Stent System
Male ArmActive comparatorMale Gender with diagnose of ST segment Elevation Acute Myocardial Infarction (STEMI). Interventions: Angiography, thrombus aspiration, optical coherence tomography and percutaneous coronary intervention, implantation of XIENCE PRIME Everolimus Eluting Coronary Stent. Angiography and Optical Coherence Tomography follow up at 9 months.
Receives: Procedure: Percutaneous Coronary Intervention; Device: XIENCE PRIME Everolimus Eluting Coronary Stent System

What is being measured

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

  1. percentage of ruptured or eroded plaques at infarct related lesion as assessed by OCT before PCI

    To assess gender differences in the percentage of ruptured or eroded plaques at infarct related lesion as assessed by OCT before PCI.

    Measured: within 6 hours from symptoms onset

Secondary outcomes (7)
  1. Minimal Fibrous Cap Thickness (µm) at infarct-related lesion.

    To assess gender differences in Minimal Fibrous Cap Thickness at infarct related lesion.

    Measured: within 6 hours from symptoms onset

  2. Presence and type of thrombus at culprit site

    To assess gender differences in thrombus type at culprit site

    Measured: within 6 hours from symptoms onset

  3. Number of Thin Cat Fibroatheroma (TCFA) (<65 µM) in the scanned segment.

    To assess gender difference in TCFA number in culprit site

    Measured: within 6 hours from symptoms onset

  4. percent of incompletely apposed-uncovered struts

    to assess gender difference in % incompletely apposed/uncovered struts at 9 months follow up by OCT

    Measured: 9 months

  5. percent net volume obstruction

    To assess gender difference in % of stent volume obstruction by OCT at 9 months follow up

    Measured: 9 months

  6. percent abnormal intraluminal tissue

    To assess gender difference in % of abnormal intraluminal tissue by OCT at 9 months follow up

    Measured: 9 months

  7. percent of covered stent struts by OCT

    To assess gender differences in the percentage of covered stent struts by OCT at 9 months follow up.

    Measured: 9 months

Timeline

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

  1. First posted16 Oct 2015 (estimated)
  2. Study startMar 2011
  3. Primary completionJun 2012
  4. Study completionSep 2014

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 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
140 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02577965
Sponsor's protocol ID
5/01/2011-2
Acronym
OCTAVIA
Status last verified
Oct 2015
First submitted
15 Sep 2014
Last updated
16 Oct 2015
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Percutaneous Coronary Intervention and XIENCE PRIME Everolimus Eluting Coronary Stent System in people with Acute Myocardial Infarction, run by A.O. Ospedale Papa Giovanni XXIII.

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 3 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: finished, as of the sponsor's last update on 16 Oct 2015. Status can change between updates, so confirm with the study contact before making plans.

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.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

percentage of ruptured or eroded plaques at infarct related lesion as assessed by OCT before PCI (time frame: within 6 hours from symptoms onset). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 16 Oct 2015.

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