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Rapid Inflation/Deflation Compared With Prolonged High-Pressure Balloon Inflation (INFLATION/DE)

Primary Purpose

Coronary Artery Disease, Coronary Stent Occlusion

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Prolonged inflation
Rapid inflation
Sponsored by
Central Arkansas Veterans Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring stents, angioplasty, balloon, coronary, coronary artery stenosis, optical coherence tomography

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients >18 years old with coronary disease with clinical indication for single stent placement in a lesion with a 2.5-3.5 mm diameter and who require OCT for determination of effective stent placement .

Exclusion Criteria:

1. ST segment elevation myocardial infarction 2. Chronic total occlusion 3. Bifurcation lesion or major side branch (>2.5 mm) within the stented area 4. Need for overlapping stents 5. Clinical instability including cardiogenic shock 6. Inability to give informed consent 7. Chronic kidney disease with serum creatinine >1.8 mg/dL 8. Unprotected left main stenosis

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Sites / Locations

  • John L. McClellan Memorial Veterans Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Rapid

Prolonged

Arm Description

The rapid inflation method will consist of reaching an operator determined high-pressure (16 atm) with the stent-deployment balloon and maintaining it the duration of time determined by the operator but <30 sec if the balloon is fully inflated and longer only if the balloon requires a longer duration to become fully inflated.

Prolonged inflation will be performed at high pressure(16 atm)and maintained for 30 sec with <0.3 atm drop during that period.

Outcomes

Primary Outcome Measures

Number of unapposed stent struts
Minimal luminal stent area
Minimal lumen stent diameter

Secondary Outcome Measures

Number of unapposed stent struts/mm of stent
% of patients with complete stent apposition
Symptomatic ischemia requiring balloon deflation
Serious arrhythmia

Full Information

First Posted
September 18, 2013
Last Updated
February 9, 2023
Sponsor
Central Arkansas Veterans Healthcare System
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1. Study Identification

Unique Protocol Identification Number
NCT01952873
Brief Title
Rapid Inflation/Deflation Compared With Prolonged High-Pressure Balloon Inflation
Acronym
INFLATION/DE
Official Title
Rapid Inflation/Deflation Compared With Prolonged High-Pressure Balloon Inflation on the Results of Stent Deployment
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2024 (Anticipated)
Primary Completion Date
December 2028 (Anticipated)
Study Completion Date
December 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Central Arkansas Veterans Healthcare System

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
It is universally accepted that high-pressure balloon inflation is required to most effectively deploy a coronary balloon-expandable stent. However, there is not consensus nor are there any guidelines regarding the method of balloon inflation, particularly the duration of inflation. Underexpansion and strut malapposition after stent deployment are among the most powerful predictors for adverse vessel outcomes. High-pressure inflation for stent deployment is effective to optimally expand the stent, but unlike in vitro testing in air, there are poorly distensible plaque elements that may not instantaneously yield to the balloon pressure. However, these elements may ultimately yield to prolonged inflation. Most clinical interventional cardiologists inflate for a relatively short period (15-30 sec). The investigators have noted that when balloon pressure is maintained at a certain pressure level it tends to decrease over time, and may require 60-180 or more seconds to maintain pressure stability. This finding implies that plaque elements are yielding slowly over time to the increased pressure, thus increasing expansion, and suggests that a prolonged inflation until balloon pressure stabilizes is more effective than a rapid inflation/deflation sequence to fully expand and appose the stent to the vessel wall. At present there is no consensus on stent deployment strategy. It is our hypothesis that prolonged inflation is superior to the more commonly used strategy of rapid inflation/deflation. Optimal coherence tomography (OCT), a novel technology that measures near-infrared light reflections and translates them into a 2D image, has an axial resolution nearly 10-times that of intravascular ultrasound (IVUS). Thus it is possible to examine the extent of stent apposition and stent expansion using this modality. The current randomized trial tests the hypothesis that prolonged balloon inflation until a stable balloon pressure is maintained is more effective than a rapid inflation/deflation sequence when performed to the same balloon inflation pressure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Coronary Stent Occlusion
Keywords
stents, angioplasty, balloon, coronary, coronary artery stenosis, optical coherence tomography

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rapid
Arm Type
Active Comparator
Arm Description
The rapid inflation method will consist of reaching an operator determined high-pressure (16 atm) with the stent-deployment balloon and maintaining it the duration of time determined by the operator but <30 sec if the balloon is fully inflated and longer only if the balloon requires a longer duration to become fully inflated.
Arm Title
Prolonged
Arm Type
Experimental
Arm Description
Prolonged inflation will be performed at high pressure(16 atm)and maintained for 30 sec with <0.3 atm drop during that period.
Intervention Type
Other
Intervention Name(s)
Prolonged inflation
Intervention Description
Prolonged inflation will be performed at high pressure(16 atm)and maintained for 30 sec with <0.3 atm drop during that period.
Intervention Type
Other
Intervention Name(s)
Rapid inflation
Intervention Description
The rapid inflation method will consist of reaching an operator determined high-pressure (16 atm) with the stent-deployment balloon and maintaining it the duration of time determined by the operator but <30 sec if the balloon is fully inflated and longer only if the balloon requires a longer duration to become fully inflated.
Primary Outcome Measure Information:
Title
Number of unapposed stent struts
Time Frame
Day 1 Within first hour after after stent deployment
Title
Minimal luminal stent area
Time Frame
Day 1 Within first hour after after stent deployment
Title
Minimal lumen stent diameter
Time Frame
Day 1 Within first hour after after stent deployment
Secondary Outcome Measure Information:
Title
Number of unapposed stent struts/mm of stent
Time Frame
Day 1 Within first hour after stent deployment
Title
% of patients with complete stent apposition
Time Frame
Day 1 Within first hour after stent deployment
Title
Symptomatic ischemia requiring balloon deflation
Time Frame
Intra-procedure
Title
Serious arrhythmia
Time Frame
Intra-procedure and first hour post-PCI

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients >18 years old with coronary disease with clinical indication for single stent placement in a lesion with a 2.5-3.5 mm diameter and who require OCT for determination of effective stent placement . Exclusion Criteria: 1. ST segment elevation myocardial infarction 2. Chronic total occlusion 3. Bifurcation lesion or major side branch (>2.5 mm) within the stented area 4. Need for overlapping stents 5. Clinical instability including cardiogenic shock 6. Inability to give informed consent 7. Chronic kidney disease with serum creatinine >1.8 mg/dL 8. Unprotected left main stenosis -
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kristin Miller, RN
Phone
501-257-5893
Email
kristin.miller4@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barry F Uretsky, M.D.
Organizational Affiliation
Central Arkansas Veterans' Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
John L. McClellan Memorial Veterans Hospital
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72205
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kristin Miller, RN
Phone
501-257-5893
Email
kristin.miller4@va.gov
First Name & Middle Initial & Last Name & Degree
Barry F Uretsky, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
23436559
Citation
Cook JR, Mhatre A, Wang FW, Uretsky BF. Prolonged high-pressure is required for optimal stent deployment as assessed by optical coherence tomography. Catheter Cardiovasc Interv. 2014 Mar 1;83(4):521-7. doi: 10.1002/ccd.24724. Epub 2013 Feb 21.
Results Reference
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Rapid Inflation/Deflation Compared With Prolonged High-Pressure Balloon Inflation

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