Routine Coronary Catheterization in Low Extremity Artery Disease Undergoing Percutaneous Transluminal Angioplasty (PIROUETTEPTA)
Primary Purpose
Peripheral Artery Disease, Coronary Artery Disease
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Systemic Strategy
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Artery Disease focused on measuring coronary artery disease, peripheral artery disease, percutaneous transluminal angioplasty, coronary angiography, revascularization, gene polymorphisms, microRNAs
Eligibility Criteria
Inclusion Criteria:
- Known LEAD (documented by previous angiography or sonography performed by the operators) admitted for elective PTA
Exclusion Criteria:
- Known CAD or unstable angina within past 3 months
- Acute myocardial infarction within past 6 months
- Known CAD status posterior percutaneous coronary intervention or bypass surgery within past 6 months
- Planning to do bypass surgery for known LEAD\
- Pregnancy
- Documented active malignancy
- Needing emergency PTA
Sites / Locations
- National Cheng Kung University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
No Intervention
Active Comparator
Arm Label
Selective Strategy
Registry
Systemic Strategy
Arm Description
non-invasive evaluation of possible myocardial ischemia by using DSE or dTS followed by coronary angiography if the test is positive for ischemia
Clinical decisions are reached by consensus of operators, patients and family as usual care
Routine coronary angiography before PTA without a previous non-invasive stress test
Outcomes
Primary Outcome Measures
Time to Composite of Major Adverse Cardiac Event (MACE)
cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and any unplanned coronary revascularization
Secondary Outcome Measures
MACE between the Screening and 30 days after PTA
cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and any unplanned coronary revascularization
Time to Composite of major coronary events
fatal or nonfatal myocardial infarction, recurrent angina pectoris, and any unplanned coronary revascularization
Full Information
NCT ID
NCT02169258
First Posted
June 19, 2014
Last Updated
September 23, 2015
Sponsor
National Cheng-Kung University Hospital
Collaborators
Tainan Municipal Hospital, E-DA Hospital, Kaohsiung Medical University, National Taiwan University Hospital, Buddhist Tzu Chi General Hospital, Far Eastern Memorial Hospital, University of Alberta
1. Study Identification
Unique Protocol Identification Number
NCT02169258
Brief Title
Routine Coronary Catheterization in Low Extremity Artery Disease Undergoing Percutaneous Transluminal Angioplasty
Acronym
PIROUETTEPTA
Official Title
Prognostic Impact of ROUtine Coronary CathETerization in Low Extremity ArTEry Disease Undergoing Percutaneous Transluminal Angioplasty (PIROUETTE-PTA Study)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cheng-Kung University Hospital
Collaborators
Tainan Municipal Hospital, E-DA Hospital, Kaohsiung Medical University, National Taiwan University Hospital, Buddhist Tzu Chi General Hospital, Far Eastern Memorial Hospital, University of Alberta
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The prevalence of significant and complex obstructive coronary artery disease (CAD) is high in patients who have low extremity artery disease (LEAD).
Long-term prognosis of LEAD undergoing percutaneous transluminal angioplasty (PTA) remains poor and CAD is an independent predictor of total mortality after PTA.
This prospective randomized controlled trial will evaluate the prognostic effects of routine versus selective coronary angiography before PTA for LEAD and elucidate the potential mechanism.
Detailed Description
participants
eligible participants are randomly assigned to systemic strategy or selective strategy
participants allocated to systemic strategy will receive routine coronary angiography before PTA without a previous non-invasive stress test
subjects allocated to selective strategy will undergo non-invasive evaluation of possible myocardial ischemia by using dobutamine stress echocardiography (DSE) or dipyridamole thallium 201 myocardial perfusion scintigraphy (dTS) followed by coronary angiography if the test is positive for ischemia
participants who are not willing to be randomized will be included in the registration group
revascularization
a staged approach (myocardial revascularization first followed by PTA) and simultaneous approach (percutaneous coronary intervention immediately followed by PTA at the same time if clinically suitable) are both allowed
the duration from revascularization to PTA should be within 60 days
percutaneous coronary intervention is performed at the time of coronary angiography, using bare metal or drug-eluting stents
blood sampling, genotyping, and measurement of biomarkers and microRNA
a. bood samples (20 mL) are obtained from peripheral arteries in all study subjects before PTA and 10 mL after PTA and are prepared and stored for enzyme-linked immunosorbent assay (ELISA), genotyping and measurement of microRNAs in plasma and peripheral blood mononuclear cells
outcome follow-up a. clinical outcomes are obtained by chart review if the patient is still in the hospital and followed up by clinic visit, telephone call or direct contact with participants or subjects' family at 30 days after indexed PTA if the patient has been discharged from the hospital and every 6 months thereafter
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Artery Disease, Coronary Artery Disease
Keywords
coronary artery disease, peripheral artery disease, percutaneous transluminal angioplasty, coronary angiography, revascularization, gene polymorphisms, microRNAs
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
700 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Selective Strategy
Arm Type
Placebo Comparator
Arm Description
non-invasive evaluation of possible myocardial ischemia by using DSE or dTS followed by coronary angiography if the test is positive for ischemia
Arm Title
Registry
Arm Type
No Intervention
Arm Description
Clinical decisions are reached by consensus of operators, patients and family as usual care
Arm Title
Systemic Strategy
Arm Type
Active Comparator
Arm Description
Routine coronary angiography before PTA without a previous non-invasive stress test
Intervention Type
Procedure
Intervention Name(s)
Systemic Strategy
Other Intervention Name(s)
Routine Coronary Angiography before PTA
Intervention Description
Significant CAD needing further revascularization is defined as patients who have luminal stenosis > 70% of the major epicardial vessels and bypass graft vessel or their major branches (> 50% for left main trunk or in-stent restenotic lesion) with reference vessel larger than 2.5 mm in diameter and moderate area of vulnerable myocardium for ischemia. Intermediate stenotic lesions should be determined if they are hemodynamic significant by fractional flow reserve (FFR) (<=0.8). The choice of revascularization procedure, either percutaneous coronary intervention or coronary artery bypass surgery, depends on operator's or cardiovascular team's suggestion and patient's decision.
Primary Outcome Measure Information:
Title
Time to Composite of Major Adverse Cardiac Event (MACE)
Description
cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and any unplanned coronary revascularization
Time Frame
up to 48 months
Secondary Outcome Measure Information:
Title
MACE between the Screening and 30 days after PTA
Description
cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and any unplanned coronary revascularization
Time Frame
30 days after indexed PTA
Title
Time to Composite of major coronary events
Description
fatal or nonfatal myocardial infarction, recurrent angina pectoris, and any unplanned coronary revascularization
Time Frame
Up to 48 months
Other Pre-specified Outcome Measures:
Title
Time to death from any cause
Description
total mortality
Time Frame
Up to 48 months
Title
Time to congestive heart failure requiring hospitalization
Description
congestive heart failure requiring hospitalization
Time Frame
Up to 48 months
Title
Time to any coronary revascularization
Description
planned or unplanned coronary revascularization
Time Frame
Up to 48 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Known LEAD (documented by previous angiography or sonography performed by the operators) admitted for elective PTA
Exclusion Criteria:
Known CAD or unstable angina within past 3 months
Acute myocardial infarction within past 6 months
Known CAD status posterior percutaneous coronary intervention or bypass surgery within past 6 months
Planning to do bypass surgery for known LEAD\
Pregnancy
Documented active malignancy
Needing emergency PTA
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ting-Hsing Chao, MD
Phone
886-6-2353535
Ext
2382
Email
chaoth@mail.ncku.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ting-Hsing Chao, MD
Organizational Affiliation
National Cheng-Kung University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cheng Kung University Hospital
City
Tainan
ZIP/Postal Code
704
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ting-Hsing Chao, MD
Phone
886-6-2353535
Ext
2382
Email
chaoth@mail.ncku.edu.tw
First Name & Middle Initial & Last Name & Degree
Cheng-Han Lee, MD/PhD
12. IPD Sharing Statement
Citations:
PubMed Identifier
24357434
Citation
Chang SH, Tsai YJ, Chou HH, Wu TY, Hsieh CA, Cheng ST, Huang HL. Clinical predictors of long-term outcomes in patients with critical limb ischemia who have undergone endovascular therapy. Angiology. 2014 Apr;65(4):315-22. doi: 10.1177/0003319713515544. Epub 2013 Dec 19.
Results Reference
background
PubMed Identifier
19729114
Citation
Monaco M, Stassano P, Di Tommaso L, Pepino P, Giordano A, Pinna GB, Iannelli G, Ambrosio G. Systematic strategy of prophylactic coronary angiography improves long-term outcome after major vascular surgery in medium- to high-risk patients: a prospective, randomized study. J Am Coll Cardiol. 2009 Sep 8;54(11):989-96. doi: 10.1016/j.jacc.2009.05.041.
Results Reference
background
PubMed Identifier
20207271
Citation
Duran NE, Duran I, Gurel E, Gunduz S, Gol G, Biteker M, Ozkan M. Coronary artery disease in patients with peripheral artery disease. Heart Lung. 2010 Mar-Apr;39(2):116-20. doi: 10.1016/j.hrtlng.2009.07.004.
Results Reference
background
PubMed Identifier
26927298
Citation
Chen IC, Lee CH, Chao TH, Tseng WK, Lin TH, Chung WJ, Li JK, Huang HL, Liu PY, Chao TK, Chu CY, Lin CC, Hsu PC, Lee WH, Lee PT, Li YH, Tseng SY, Tsai LM, Hwang JJ. Impact of routine coronary catheterization in low extremity artery disease undergoing percutaneous transluminal angioplasty: study protocol for a multi-center randomized controlled trial. Trials. 2016 Feb 29;17(1):112. doi: 10.1186/s13063-016-1237-0.
Results Reference
derived
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Routine Coronary Catheterization in Low Extremity Artery Disease Undergoing Percutaneous Transluminal Angioplasty
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