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The Effect of Catheter Ablation on Sexual Dysfunctio

Not Applicable
Conditions
Atrial Fibrillation
Erectile Dysfunction
Premature Ejaculation
Female Sexual Dysfunction
Reproductive Health and Childbirth - Other reproductive health and childbirth disorders
Cardiovascular - Other cardiovascular diseases
Registration Number
ACTRN12624000994583
Lead Sponsor
Alfred Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
346
Inclusion Criteria

All patients with persistent or paroxysmal AF referred for either catheter ablation or medical therapy.
AF documented at least once in the past 6 months.

Exclusion Criteria

Severe medical comorbidity the limits life expectancy to < 6 months

Unwilling or unable to consent.

Unwilling to unable to complete follow-up.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in Sexual Quality of Life[Change in Overall Sexual QoL Baseline (pre-intervention), and 6 months]
Secondary Outcome Measures
NameTimeMethod
Change in Sexual Quality of Life[The Sexual Health Inventory for Men Baseline (pre-intervention), and 6 months];Change in AF severity [NYHA functional class Baseline pre ablation and at 6 months];Change in AF severity[Canadian Cardiovascular Society AF Score Baseline pre ablation and 6 months post];Psychological Mood[The Depression, Anxiety, Stress Scale (DASS - 21) Baseline Pre Ablation and 6 months post];Change in Sexual Quality of Life[The Female Sexual Function Index Score baseline (pre intervention), and 6 months];Change in Sexual Quality of Life[The Sexual Quality of LIfe - Female Questionnaire Baseline (pre intervention), and 6 months];Change in Sexual Quality of Life[The Sexual Quality of life - Male score baseline (pre-intervention), and 6 months. ];Change in Sexual Quality of Life[the International Index of erectile dysfunction score Baseline (pre-intervention), and 6 months];Change in Sexual Quality of Life[The Premature Ejaculation Diagnostic Tool Baseline (pre-intervention), and 6 months]
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