IX-01 Effect on Intravaginal Ejaculatory Latency Time (IELT) & Patient

See also
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Completed	`NCT01184105` - A Safety and Tolerability of PSD502 (a Topical Anesthetic) in the Treatment of Premature Ejaculation	Phase 1
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Completed	`NCT02939495` - The Efficacy and Safety of Dapoxetine/Sildenafil Combination Therapy	Phase 4
Completed	`NCT02572037` - Research and Clinical Value of New Classification for Premature Ejaculation: Multi-Center Research
Recruiting	`NCT02581826` - Safety and Efficacy of Silodosin in the Treatment of Premature Ejaculation	Phase 2
Terminated	`NCT00983736` - Study to Evaluate Efficacy and Safety in Male Subjects With Premature Ejaculation	Phase 3
Completed	`NCT00556478` - Efficacy, Safety and Tolerability of PSD502 (a Topical Anesthetic) in the Treatment Premature Ejaculation	Phase 2/Phase 3
Completed	`NCT00549211` - A First Time in Human Study in Healthy Male Volunteers for Compound GSK557296.	Phase 1
Not yet recruiting	`NCT05556083` - Sildenafil Added Effect in Dapoxetine Non-responding Mono-symptomatic Premature Ejaculation (PE)	Phase 2
Completed	`NCT03304808` - Efficacy of a New Behavioral Treatment for Premature Ejaculation Using a Masturbation Aid Device: Star-Stop 3.0	N/A
Completed	`NCT00861484` - Proof of Mechanism in ELT	Phase 1
Completed	`NCT02984592` - Effect of Exercise on Premature Ejaculation	N/A
Recruiting	`NCT02571101` - A Phase 2 Study of On-demand Therapy With Clomipramine and Sildenafil Combination in Premature Ejaculation	Phase 2
Completed	`NCT03174470` - Safety Demonstration of Increasing Intensities of Electrical Stimulation Delivered to The Bulbospongiosus Muscle	N/A
Completed	`NCT02794454` - A Study to Evaluate Efficacy of Investigational Product HeezOn Ultra -1/ HeezOn Ultra-2 on Male Sexual Health	N/A
Completed	`NCT02297152` - A New Treatment for Premature Ejaculation?	N/A
Not yet recruiting	`NCT00656552` - Safety and Efficacy of Escitalopram in the Treatment of Premature Ejaculation	Phase 0
Recruiting	`NCT04703127` - Effectiveness and Tolerability of the On-demand Use of Combined Dapoxetine With Tadalafil and Combined Dapoxetine With Lidocaine 5% Spray in Treatment of Patients With Lifelong Premature Ejaculation and Non-responding to Dapoxetine Alone.	Phase 3

NCT number	NCT02232425
Study type	Interventional
Source	Ixchelsis Limited
Contact
Status	Completed
Phase	Phase 2
Start date	September 2014
Completion date	October 2015

IX-01 Effect on Intravaginal Ejaculatory Latency Time (IELT) and Patient Reported Outcomes in Men With Premature Ejaculation (PE)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms