Discontinuation of Dapoxetine Treatment in Patients With Premature Ejaculation

Sponsor
Pusan National University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03018743
Collaborator
(none)
200
1
36
5.6

Study Details

Study Description

Brief Summary

Premature ejaculation (PE) has been known as one of the most common male sexual dysfunction.

Until now dapoxetine is the only approved medical treatment option and there is no second line therapy in case of no-response or refuse to dapoxetine, a comprehensive evaluation of the factors that lead to dropout is needed especially in a real-practice setting.

With this background, investigators are going to assesse the discontinuation rate of dapoxetine treatment in patients with PE and the reasons for discontinuation in a clinical setting throughout a follow-up period of 2 years.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Premature ejaculation (PE) has been known as one of the most common male sexual dysfunction. PE can deteriorate sexual satisfaction and quality of life of the patients and their partners. Recently, the International Society for Sexual Medicine (ISSM) gave a definition that PE is a 'male sexual dysfunction characterized by ejaculation that always or nearly always occurs prior to or within 1 min of vaginal penetration from the first sexual experience (lifelong PE), or a clinically significant reduction in latency time, often to about 3 min or less (acquired PE)' . Until now, several treatment modalities for PE have been introduced. Psychological/behavioral; pharmacologic therapies, including selective serotonin reuptake inhibitors (SSRIs), tricyclic antidepressants, tramadol, phosphodiesterase 5 inhibitor, alpha 1-andreoreceptor antagonists; topical anaesthetics, and even surgical treatments have been used for PE in practice. Dapoxetine is the first oral pharmacological agent developed for the treatment of PE and the only SSRI approved in more than 60 countries for PE. The introduction of dapoxetine was accompanied with high expectation because of the optimal efficacy/ safety profile showed in the phase 3 trials. However, several clinical studies using depoxetine confirmed the efficacy in increasing IELT, it reveals significant dropout rate likely which was shown in the treatment using off-label SSRIs. Despite high efficacy and safety, discontinuation rate of dapoxetine is high compared to PDE5 inhibitors in patients with erectile dysfunction (ED).

Until now dapoxetine is the only approved medical treatment option and there is no second line therapy in case of no-response or refuse to dapoxetine, a comprehensive evaluation of the factors that lead to dropout is needed especially in a real-practice setting. With this background, investigators will assesse the discontinuation rate of dapoxetine treatment in patients with PE and the reasons for discontinuation in a clinical setting throughout a follow-up period of 2 years.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Discontinuation of Dapoxetine Treatment in Patients With Premature Ejaculation: a 2-year Prospective Observational Study
Study Start Date :
Jan 1, 2017
Anticipated Primary Completion Date :
Jan 1, 2019
Anticipated Study Completion Date :
Jan 1, 2020

Arms and Interventions

Arm Intervention/Treatment
dapoxetine treatment group

Consecutive patients who seek medical treatment for PE will be enrolled in the study.

Drug: Dapoxetine
Patients receive dapoxetine (taken 1-3 hours before sexual intercourse) 30mg as needed. A dose escalation to 60mg will be consented after 1 month in case of low efficacy. Patients will be re-evaluated 1, 3, 6, 12, and 24 months after initiating therapy regarding the treatment status and the reasons for treatment discontinuation in the case of discontinuation. If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.
Other Names:
  • Priligy
  • Outcome Measures

    Primary Outcome Measures

    1. Discontinuation rate of dapoxetine treatment [1 month after initiating therapy]

      Patients will be evaluated 1 month after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    2. Discontinuation rate of dapoxetine treatment [3 months after initiating therapy]

      Patients will be evaluated 3 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    3. Discontinuation rate of dapoxetine treatment [6 months after initiating therapy]

      Patients will be evaluated 6 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    4. Discontinuation rate of dapoxetine treatment [12 months after initiating therapy]

      Patients will be evaluated 12 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    5. Discontinuation rate of dapoxetine treatment [24 months after initiating therapy]

      Patients will be evaluated 24 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    Secondary Outcome Measures

    1. Reasons of discontinuation of dapoxetine treatment [1 month after initiating therapy]

      Patients will be evaluated 1 month after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. The secondary outcome measures are the reasons of discontinuation of dapoxetine treatment (ex, high cost, low efficacy, side effects, etc) If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    2. Reasons of discontinuation of dapoxetine treatment [3 months after initiating therapy]

      Patients will be evaluated 3 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. The secondary outcome measures are the reasons of discontinuation of dapoxetine treatment (ex, high cost, low efficacy, side effects, etc) If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    3. Reasons of discontinuation of dapoxetine treatment [6 months after initiating therapy]

      Patients will be evaluated 6 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. The secondary outcome measures are the reasons of discontinuation of dapoxetine treatment (ex, high cost, low efficacy, side effects, etc) If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    4. Reasons of discontinuation of dapoxetine treatment [12 months after initiating therapy]

      Patients will be evaluated 12 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. The secondary outcome measures are the reasons of discontinuation of dapoxetine treatment (ex, high cost, low efficacy, side effects, etc) If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    5. Reasons of discontinuation of dapoxetine treatment [24 months after initiating therapy]

      Patients will be evaluated 24 months after initiating therapy regarding the treatment status (whether they treat or drop-out) for treatment discontinuation in the case of discontinuation. The secondary outcome measures are the reasons of discontinuation of dapoxetine treatment (ex, high cost, low efficacy, side effects, etc) If patients missed any visits, they will be contacted by telephone or mail to collect their treatment data.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years to 65 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • men without history of dapoxetine treatment;

    • 19 years old; and involvement in a stable,

    • monogamous relationship with a female sexual partner

    Exclusion Criteria:
    • penile anatomical deformity;

    • spinal cord injury;

    • radical prostatectomy;

    • pelvic organ surgery;

    • diagnosis of another sexual disorder except ED;

    • an uncontrolled psychiatric disorder;

    • history of major hematological, renal, or hepatic abnormalities;

    • a history of alcoholism or substance abuse;

    • organic illness causing limitations in assuming SSRIs

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Urology, Pusan National University Hospital Busan Korea, Republic of 602-739

    Sponsors and Collaborators

    • Pusan National University Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Hyun Jun Park, Associate Professor, Pusan National University Hospital
    ClinicalTrials.gov Identifier:
    NCT03018743
    Other Study ID Numbers:
    • PNU-Dapoxetine
    First Posted:
    Jan 12, 2017
    Last Update Posted:
    Jan 12, 2017
    Last Verified:
    Jan 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 12, 2017