The Efficacy and Safety of Dapoxetine/Sildenafil Combination Therapy (DAP-SPEED)

Neutec Ar-Ge San ve Tic

Status and phase

Completed

Phase 4

Conditions

Erectile Dysfunction

Premature Ejaculation

Treatments

Drug: Dapoxetine/Sildenafil 30/50 mg film coated tablet

Study type

Interventional

Funder types

Industry

Identifiers

NCT02939495

16-NEU-1 (Other Identifier)

NEU-16.12

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy and safety of Dapoxetine/Sildenafil 30/50 mg film-coated tablet in the treatment of men with premature ejaculation and erectile dysfunction.

Full description

During 4-weeks treatment period, patients will take one Dapoxetine/Sildenafil 30/50 mg film coated tablet 1-3 hours before sexual intercourse.

Study drug should not be used more than 1 tablet every 24 hours during the treatment.

Enrollment

75 patients

Sex

Male

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

18-64 years old men,
Participants must be heterosexual males and in a stable monogamous sexual relationship with a female partner for at least 6 months and will continue throughout the study,
Clinical diagnosis of erectile dysfunction, IIEF score ≤21,
Premature Ejaculation Diagnostic Tool (PEDT) score must be ≥11
Patients with life-long PE and acquired PE according to the description of International Society for Sexual Medicine (ISSM) ,
The patient and his partner must have sexual intercourse twice a week for the duration of the study,
Commitment to comply with the study protocol,
Patients who sign informed consent form (ICF).

Exclusion criteria

History of medical events such as surgical interventions or neurologic conditions (e.g., multiple sclerosis), trauma, or infections that are associated with the development of symptoms of premature ejaculation (PE) and considered a potential cause of PE,
Having genital abnormalities, except penile curvature unless not prevent sexual intercourse,
Developed ED or PE due to drug use or quit taking drugs,
Any conditions that prevent sexual intercourse with partners
History of epilepsy,
Severe renal insufficiency,
Liver disease,
History of in last 6 months stroke, myocard infarction, cardiac insufficiency (New York Cardiovascular Associates (NYCA) phase II-IV), AV block or message disorder such as sick sinus syndrome, severe ischemic cardiac disease, syncope, unstable angına, life-threatening arrhythmia or hypotension,
Non-Arteritic Anterior ischemic optic neuropathy,
Patients who are not eligible to have sexual intercourse due to existing health problems,
Autonomic neuropathy, retinitis pigmentosa, blood diseases, active peptic ulcer, abnormalities in ECG, severe systemic disease that cannot be controlled,
Systolic/Diastolic blood pressure at rest <90/50mmHg and 170/100mmHg<
History of allergy to Selective Serotonine Reuptake Inhibitor (SSRI) and phosphodiesterase inhibitor drugs,
Continuing to use or quitted in last 3 months of Monoamine oxidase inhibitor (MAOI), Thioridazine, Serotonine Reuptake Inhibitor (SSRI), Selective-Norepinephrin Reuptake Inhibitor (SNRI), Serotonergic drug/herbal product, tricyclic antidepressant and atypical antipsychotic drugs,
Use of nitrates, alfa blockers, vasodilators, ketoconazole, itraconazole, ritonavir, saquinavir, telithromycin, nefazodone, nelfinavir, atazanavir, cimetidine, erithromicin, clarithromycin, fluconazole, amprenavir, fosamprenavir, aprepitant, verapamil, diltiazem, any kind of vasodilator, antiplatelet, anticoagulant, dapoxetine, PDE5 inhibitor, alcohol and stimulant drug,
Patients on a different therapy (behavioral therapy or other drugs that are applied locally) for PE treatment
During the study, the possibility of taking medication which may affect the study drug's pharmacokinetic/pharmacodynamic properties
Patients who are defining symptoms of prostatitis clinically
Thyroid hormone disorders