Evaluation for Restoration of Erectile Dysfunction After Cardioversion Treatment Trial

NCT ID: NCT02742896

Last Updated: 2024-04-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2013-12-31

Study Completion Date

2019-10-01

Brief Summary

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Erectile and Cognitive function by using the questionnaire and assessment form before sinus conversion

Detailed Description

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Sinus conversion by electrical cardioversion increase cardiac output and systemic perfusion. According to recent reports, maintenance of sinus rhythm increase systemic perfusion which leads to improve renal function. Therefore, we hypothesized that sinus conversion of patients with atrial fibrillation will increase systemic perfusion which might improve the erectile dysfunction and cognitive dysfunction.

Conditions

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Erectile Dysfunction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Restoration of Erectile dysfunction

The changes of erectile function by using official questionnaire-The International Index of Erectile Function (IIEF)-5 1 year after conversion to sinus rhythm.

Erectile dysfunction

Intervention Type OTHER

The changes of erectile function by using official questionnaire-The International Index of Erectile Function (IIEF)-5 1 year after conversion to sinus rhythm.

The changes of cognitive function by using validated assessment form-The Montreal Cognitive assessment (MoCA) 1 year after conversion to sinus rhythm.

Interventions

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Erectile dysfunction

The changes of erectile function by using official questionnaire-The International Index of Erectile Function (IIEF)-5 1 year after conversion to sinus rhythm.

The changes of cognitive function by using validated assessment form-The Montreal Cognitive assessment (MoCA) 1 year after conversion to sinus rhythm.

Intervention Type OTHER

Other Intervention Names

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official questionnaire

Eligibility Criteria

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Inclusion Criteria

* Patients scheduled to electrical cardioversion

Exclusion Criteria

* Patients have taken any medication for erectile dysfunction or who have got any operation already or are scheduled to do.
* More than moderate degree of cognitive dysfunction
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yong Seog Oh

OTHER

Sponsor Role lead

Responsible Party

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Yong Seog Oh

professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Yong Seog Oh, MD

Role: PRINCIPAL_INVESTIGATOR

Seoul St Mary hospital

Locations

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Seoul St Mary's Hospital

Seoul, Seo Ch-gu, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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ERECT

Identifier Type: -

Identifier Source: org_study_id

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