- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02292030
Cardioversion of Atrial Fibrillation Accompanied by Chronic Heart Faliure
November 12, 2014 updated by: Wei Liu, Harbin Medical University
Cardioversion of Atrial Fibrillation Accompanied by Chronic Heart Faliure With or Without HTEA
The purpose of this study is to explore the efficacy of low energy cardioversion on atrial fibrillation accompanied with chronic heart failure treated with HTEA or usual medicine.
Study Overview
Detailed Description
The purpose of this study is to explore the efficacy of low energy (30J) cardioversion on atrial fibrillation accompanied with chronic heart failure treated with HTEA or usual medicine.
Study Type
Observational
Enrollment (Anticipated)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Heilongjiang
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Harbin, Heilongjiang, China, 150001
- Recruiting
- The First Affiliated Hospital of Harbin Medical University
-
Contact:
- Xiaohui Ren
- Phone Number: 86-451-85552320
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Harbin, Heilongjiang, China, 150001
- Recruiting
- Ren Xiaohui
-
Contact:
- Xiaohui Ren
- Phone Number: 86-85552320
- Email: renxiaohui2004@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
congestive heart failure.
Description
Inclusion Criteria:
- congestive heart failure accompanied by atrial fibrillation.
Exclusion Criteria:
- Valvular heart diseases.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
cardioversion+HTEA
Heart failure patients accompanied by atrial fibrillation receive the treatment of cardioversion+HTEA.
|
usually high thoracic epidural anesthesia
Other Names:
|
|
only cardioversion
Heart failure patients accompanied by atrial fibrillation receive the treatment of cardioversion, but not with HTEA.
|
usually high thoracic epidural anesthesia
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
recurrence of atrial fibrillation
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2014
Primary Completion (Anticipated)
October 1, 2015
Study Completion (Anticipated)
October 1, 2015
Study Registration Dates
First Submitted
November 9, 2014
First Submitted That Met QC Criteria
November 12, 2014
First Posted (Estimate)
November 17, 2014
Study Record Updates
Last Update Posted (Estimate)
November 17, 2014
Last Update Submitted That Met QC Criteria
November 12, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- dong hao
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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