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Image Fusion of SPECT MPI and Fluoroscopy Venography to Guide LV Lead Placement for Improved CRT Response (GUIDE-CRT II) (GUIDE-CRT)

Primary Purpose

Chronic Heart Failure

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Image fusion of SPECT MPI and fluoroscopy venography
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Heart Failure focused on measuring cardiac resynchronization therapy, chronic heart failure, image fusion-guided implantation, SPECT, venogram

Eligibility Criteria

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

Inclusion Criteria:

  • Patient has signed informed consent
  • moderate to severe HF (NYHA Class II, III or IV)
  • LVEF ≤35%
  • QRS duration ≥130 ms
  • sinus rhythm

Exclusion Criteria:

  • Patient is under a minimum age requirement (<18 years old)
  • Patient has mechanical right heart valve
  • Patient has experienced unstable angina, acute MI, CABG or PCI within the past 3 months
  • Patient is on continuous or intermittent (i.e., more than two infusions per week) intravenous inotropic drug therapy
  • Patient known to have chronic permanent atrial arrhythmias (i.e., cases of long-standing atrial fibrillation of greater than 1 year, including those in which cardioversion has not been indicated or attempted).
  • Patient is enrolled in any other study
  • Patient has a life expectancy of less than 12 months
  • Women who are pregnant, or with child-bearing potential and who are not on a form of birth control
  • Patient with CRT device implanted previously
  • Patient has had a heart transplant
  • Patient has third degree AVB with normal cardiac function

Sites / Locations

  • Anhui Provincial HospitalRecruiting
  • The Affiliated Hospital of Xuzhou Medical UniversityRecruiting
  • Northern Jiangsu Province People's HospitalRecruiting
  • The First Affiliated Hospital of Dalian Medical UniversityRecruiting
  • The General Hospital of Shenyang MilitaryRecruiting
  • West China HospitalRecruiting
  • First Affiliated Hospital,Zhejiang UniversityRecruiting
  • First People's Hospital of HangzhouRecruiting
  • Sir Run Run Shaw HospitalRecruiting
  • Fu Wai HospitalRecruiting
  • Shanghai Chest HospitalRecruiting
  • Zhongshan HospitalRecruiting
  • First Affiliated Hospital Xi'an Jiaotong UniversityRecruiting
  • Xijing HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

GUIDED group

Control group

Arm Description

Image fusion of SPECT MPI and fluoroscopy venography to guide LV lead placement for improved CRT response in the guided group.

No Image fusion of SPECT MPI and fluoroscopy venography to guide LV lead placement for improved CRT response.

Outcomes

Primary Outcome Measures

Changes in LVESV
Changes in LVESV between baseline and 6-month follow-up (a continuous variable): LVESV will be assessed by echocardiography (Simpson's rule). Changes in LVESV will be compared between the two groups.

Secondary Outcome Measures

CRT response rate
The proportion of the positive CRT response in each group. A positive CRT response is defined as reduction in LVESV by ≥15% and/or LVEF increase by ≥10% at 6-month follow-up as compared to the baseline.
Changes in LVEF
LVEF will be assessed by echocardiography (Simpson's rule) and compared between the baseline and 6-month follow-up. Changes in LVEF will be compared between the two groups.
Composite clinical response rate
A positive response is defined as decrease by ≥1 NYHA class and/or improvement in 6MWD by ≥10% and/or decrease in QOL score by ≥ 9 points at 6-month follow-up. NYHA class: Changes in NYHA class at 6-month follow-up as compared to the baseline will be compared between the two groups. 6MWD: Changes in 6MWD at 6-month follow-up as compared to the baseline will be compared between the two groups. QOL: Changes in QOL score at 6-month follow-up as compared to the baseline will be compared between the two groups.
All-cause mortality and composite clinical endpoints
All-cause mortality,all-cause death and heart failure re-hospitalization by the end of study.

Full Information

First Posted
April 14, 2017
Last Updated
September 24, 2023
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Collaborators
Fu Wai Hospital, Beijing, China, Shanghai Zhongshan Hospital, Shanghai Chest Hospital, First Affiliated Hospital Xi'an Jiaotong University, Xijing Hospital, First Affiliated Hospital of Zhejiang University, Sir Run Run Shaw Hospital, First People's Hospital of Hangzhou, Anhui Provincial Hospital, The Affiliated Hospital of Xuzhou Medical University, Northern Jiangsu Province People's Hospital, West China Hospital, The First Affiliated Hospital of Dalian Medical University, General Hospital of Shenyang Military Region, Nanjing Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03125720
Brief Title
Image Fusion of SPECT MPI and Fluoroscopy Venography to Guide LV Lead Placement for Improved CRT Response (GUIDE-CRT II)
Acronym
GUIDE-CRT
Official Title
Image Fusion of SPECT MPI and Fluoroscopy Venography to Guide LV Lead Placement for Improved CRT Response (GUIDE-CRT II)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 14, 2017 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
November 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital with Nanjing Medical University
Collaborators
Fu Wai Hospital, Beijing, China, Shanghai Zhongshan Hospital, Shanghai Chest Hospital, First Affiliated Hospital Xi'an Jiaotong University, Xijing Hospital, First Affiliated Hospital of Zhejiang University, Sir Run Run Shaw Hospital, First People's Hospital of Hangzhou, Anhui Provincial Hospital, The Affiliated Hospital of Xuzhou Medical University, Northern Jiangsu Province People's Hospital, West China Hospital, The First Affiliated Hospital of Dalian Medical University, General Hospital of Shenyang Military Region, Nanjing Medical University

4. Oversight

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

5. Study Description

Brief Summary
CRT response will be significantly better using image fusion of SPECT MPI and fluoroscopy venogram to guide LV lead placement at the latest activation segment without scar than standard-of-care implantation.
Detailed Description
Chronic heart failure (CHF) is final phase of a variety of cardiovascular diseases. Epidemiological data revealed that the morbidity of CHF is 0.9% in China, and there are 300,000 new CHF patients are diagnosed each year. Moreover, the total number of CHF patients exceeded 5.5 million throughout the country. Therefore, CHF has become a seriously social and public health problem in China. Although medical treatment for CHF has achieved considerable progress, prognosis is still poor and mortality is high among end-stage HF patients. Since the 1990s, cardiac resynchronization therapy(CRT) has been applied to treat CHF, a large number of evidence-based medicine has shown that CRT brings great clinical effects; CRT mainly aims at delayed activation of left ventricular(LV) and stimulates LV in advance to restore the inter- and intra-ventricular synchrony. As a result, cardiac function, symptoms and quality of life in CHF patients improved, meanwhile mortality rate also decreases. At present, CRT is recommended in quite a number of CHF patients as class I indication. And yet, approximately 30%-40% of patients did not show response to CRT. Non-response to CRT has become a significant problem that must be solved. In recent years, researchers have tried LV multipoint pacing (MPP), transseptal left ventricular endocardial pacing and MitraClip to get some achievements. But these new techniques and CRT itself have two main failings:(1) Up to now, there is no specific suggestions about whether the patient's myocardium has too severe myocardial fibrosis and scar burden to be fit for CRT.(2)The LV mechanical dysynchronization will influence CRT effects. So far, screening CRT indications is primarily based on QRS morphology and duration on surface electrocardiogram.QRS duration≥120ms represents the presence of electrical dysynchronization, however, electrical dysynchronization is not equal to mechanical dysynchronization. The key point of CRT is to solve the mechanical dysynchronization, so estimating cardiac mechanical dysynchrony is important for predicting the CRT response; In addition, LV lead implantation site also exerts an effect on CRT response. The standard-of-care of LV lead implantation technique now just relays on coronary vein angiography showing the appropriate branch vein. This approach cannot guarantee LV lead is implanted in the latest activation site and the non-scar segment. Therefore, the following two issues are very important: how to evaluate the myocardiac scar and LV mechanical dyssynchronization using an objective, accurate, simple and economic method? and how to explore a new image which can guide LV lead to position at the latest activation and non-scar segment conveniently and accurately during procedure for improving CRT response rate? Myocardial perfusion image-phase analysis technique(MPI-PA) is a new non-invasive method to evaluate LV desynchronization,the latest activation site and myocardial scar burden. In recent years,Henneman MM and Adelstein EC reported PA technique detecting LV systolic desynchronization and LV scar burden influencing on CRT response respectively. Their study showed that the low CRT response is associated with the mild LV dyssynchrony and severe scar burden.The past five years,our center has completed a prospective, randomized, multi-center study of"SPECT guided LV Lead Placement for Incremental Benefits to CRT Efficacy"(GUIDE-CRT).We found that the CRT efficacy in SPECT-Guided group at 6 months after CRT implantation was better than that in standard-of-care implantation group(control group):the reduction in LVESV at 6 months in guided group is much more than that in control group(control 28.2ml vs guided group 48.2ml,P=0.029). The CRT response rate, defined as reduction in LVESV more than 15%, in guided group was 55.8% is higher than 47.8% in control group,but there was no statistic difference between two groups.The guiding mothodology of implanting LV lead in our previous study (GUIDE-CRT) was as following: implanter chose the branch vein to implant LV lead based on the recommended site by MPI-PA. Under this guidance, still much percentage of LV lead did not located in the recommended site. Therefore, in order to further improve the accuracy of SPECT guiding LV lead placement, our present study will use automatic fusion of coronary venogram with SPECT images to guide the implantation of LV lead precisely, and bringing incremental benefits to CRT efficacy. This new study(GUIDE-CRT II) is a prospective, randomized, multi-center trial. Applying the new image fusion of SPECT MPI and coronary venogram to guide LV lead placement at the recommended optimal position, to achieve the precise localization, to avoid blindness of standard of care implantation methods and to improve response to CRT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Heart Failure
Keywords
cardiac resynchronization therapy, chronic heart failure, image fusion-guided implantation, SPECT, venogram

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GUIDED group
Arm Type
Experimental
Arm Description
Image fusion of SPECT MPI and fluoroscopy venography to guide LV lead placement for improved CRT response in the guided group.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
No Image fusion of SPECT MPI and fluoroscopy venography to guide LV lead placement for improved CRT response.
Intervention Type
Other
Intervention Name(s)
Image fusion of SPECT MPI and fluoroscopy venography
Intervention Description
In this study, MPI-Fluoro Fusion tool is used to help the implanting physicians to precisely implant LV lead to the optimal/suboptimal venous segments in the guided group.
Primary Outcome Measure Information:
Title
Changes in LVESV
Description
Changes in LVESV between baseline and 6-month follow-up (a continuous variable): LVESV will be assessed by echocardiography (Simpson's rule). Changes in LVESV will be compared between the two groups.
Time Frame
6-month follow-up
Secondary Outcome Measure Information:
Title
CRT response rate
Description
The proportion of the positive CRT response in each group. A positive CRT response is defined as reduction in LVESV by ≥15% and/or LVEF increase by ≥10% at 6-month follow-up as compared to the baseline.
Time Frame
6-month follow-up
Title
Changes in LVEF
Description
LVEF will be assessed by echocardiography (Simpson's rule) and compared between the baseline and 6-month follow-up. Changes in LVEF will be compared between the two groups.
Time Frame
6-month follow-up
Title
Composite clinical response rate
Description
A positive response is defined as decrease by ≥1 NYHA class and/or improvement in 6MWD by ≥10% and/or decrease in QOL score by ≥ 9 points at 6-month follow-up. NYHA class: Changes in NYHA class at 6-month follow-up as compared to the baseline will be compared between the two groups. 6MWD: Changes in 6MWD at 6-month follow-up as compared to the baseline will be compared between the two groups. QOL: Changes in QOL score at 6-month follow-up as compared to the baseline will be compared between the two groups.
Time Frame
6-month follow-up
Title
All-cause mortality and composite clinical endpoints
Description
All-cause mortality,all-cause death and heart failure re-hospitalization by the end of study.
Time Frame
6-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient has signed informed consent moderate to severe HF (NYHA Class II, III or IV) LVEF ≤35% QRS duration ≥130 ms sinus rhythm Exclusion Criteria: Patient is under a minimum age requirement (<18 years old) Patient has mechanical right heart valve Patient has experienced unstable angina, acute MI, CABG or PCI within the past 3 months Patient is on continuous or intermittent (i.e., more than two infusions per week) intravenous inotropic drug therapy Patient known to have chronic permanent atrial arrhythmias (i.e., cases of long-standing atrial fibrillation of greater than 1 year, including those in which cardioversion has not been indicated or attempted). Patient is enrolled in any other study Patient has a life expectancy of less than 12 months Women who are pregnant, or with child-bearing potential and who are not on a form of birth control Patient with CRT device implanted previously Patient has had a heart transplant Patient has third degree AVB with normal cardiac function
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiangang Zou, MD,Ph.D
Phone
86-25-13605191407
Email
jgzou@njmu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiangang Zou, MD,Ph.D
Organizational Affiliation
The First Affiliated Hospital with Nanjing Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Anhui Provincial Hospital
City
Hefei
State/Province
Anhui
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ji Yan, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Ji Yan, MD,Ph.D
Facility Name
The Affiliated Hospital of Xuzhou Medical University
City
Xuzhou
State/Province
Jiangsu
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhirong Wang, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Zhirong Wang, MD,Ph.D
Facility Name
Northern Jiangsu Province People's Hospital
City
Yangzhou
State/Province
Jiangsu
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiang Gu, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Xiang Gu, MD,Ph.D
Facility Name
The First Affiliated Hospital of Dalian Medical University
City
Dalian
State/Province
Liaoning
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yunlong Xia, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Yunlong Xia, MD,Ph.D
Facility Name
The General Hospital of Shenyang Military
City
Shenyang
State/Province
Liaoning
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanchun Liang, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Yanchun Liang, MD,Ph.D
Facility Name
West China Hospital
City
Chengdu
State/Province
Sichuan
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xingbin Liu, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Xingbin Liu, MD,Ph.D
Facility Name
First Affiliated Hospital,Zhejiang University
City
Hangzhou
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liangrong Zheng, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Liangrong Zheng, MD,Ph.D
Facility Name
First People's Hospital of Hangzhou
City
Hangzhou
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yizhou Xu, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Yizhou Xu, MD,Ph.D
Facility Name
Sir Run Run Shaw Hospital
City
Hangzhou
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guosheng Fu, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Guosheng Fu, MD,Ph.D
Facility Name
Fu Wai Hospital
City
Beijing
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Keping Chen, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Keping Chen, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Xiaohan Fan, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Wei Hua, MD,Ph.D
Facility Name
Shanghai Chest Hospital
City
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruogu Li, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Ruogu Li, MD,Ph.D
Facility Name
Zhongshan Hospital
City
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yangang Su, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Yangang Su, MD,Ph.D
Facility Name
First Affiliated Hospital Xi'an Jiaotong University
City
Xi'an
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaolin Xue, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Xiaolin Xue, MD,Ph.D
Facility Name
Xijing Hospital
City
Xi'an
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bing Liu, MD,Ph.D
First Name & Middle Initial & Last Name & Degree
Bing Liu, MD,Ph.D

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22405632
Citation
Khan FZ, Virdee MS, Palmer CR, Pugh PJ, O'Halloran D, Elsik M, Read PA, Begley D, Fynn SP, Dutka DP. Targeted left ventricular lead placement to guide cardiac resynchronization therapy: the TARGET study: a randomized, controlled trial. J Am Coll Cardiol. 2012 Apr 24;59(17):1509-18. doi: 10.1016/j.jacc.2011.12.030. Epub 2012 Mar 7.
Results Reference
result
PubMed Identifier
25440593
Citation
Zhou W, Hou X, Piccinelli M, Tang X, Tang L, Cao K, Garcia EV, Zou J, Chen J. 3D fusion of LV venous anatomy on fluoroscopy venograms with epicardial surface on SPECT myocardial perfusion images for guiding CRT LV lead placement. JACC Cardiovasc Imaging. 2014 Dec;7(12):1239-48. doi: 10.1016/j.jcmg.2014.09.002. Epub 2014 Nov 5.
Results Reference
result

Learn more about this trial

Image Fusion of SPECT MPI and Fluoroscopy Venography to Guide LV Lead Placement for Improved CRT Response (GUIDE-CRT II)

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