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Premature Ejaculation clinical trials

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NCT ID: NCT02378779 Terminated - Clinical trials for Premature Ejaculation

Consultations Reason for Genital, Urinary or Psychological Humans in General Practice

GETUP
Start date: April 22, 2016
Phase: N/A
Study type: Interventional

Many male patients complain about their ejaculation: 21-30% of men aged between 18 and 59 have admitted suffering from a decrease in, or loss of control of, their ejaculation. The quality of life of patients and their partners is impaired compared to men not suffering from premature ejaculation. Economically, the impact of the disease are significant. In the year preceding the detection of premature ejaculation patients visit twice their physician. The majority of men interviewed anonymously, in their General Practitioner's ( GP's) waiting room, considered it important to talk with their GP about their sexual concerns. Almost half of them preferred that their GP initiate any discussions about sexuality. More than two thirds of the respondents would have liked their GP to signal his or her open-mindedness by directly addressing sexual topics during the consultation. In 2008 a qualitative study brought to the fore the strategies used by GPs to initiate the discussion on premature ejaculation . GPs who mentioned premature ejaculation with their patient described three attitude-related strategies and three investigative strategies.

NCT ID: NCT01917006 Terminated - Clinical trials for Premature Ejaculation

A Safety and Efficacy Study of OnabotulinumtoxinA in Premature Ejaculation

Start date: August 7, 2013
Phase: Phase 2
Study type: Interventional

This is a safety and efficacy study of OnabotulinumtoxinA for the treatment of premature ejaculation (PE) in male participants.

NCT ID: NCT00983736 Terminated - Clinical trials for Premature Ejaculation

Study to Evaluate Efficacy and Safety in Male Subjects With Premature Ejaculation

Start date: October 2009
Phase: Phase 3
Study type: Interventional

The purpose of this clinical trial is to test an experimental drug therapy called Tramadol Hydrochloride (HCl) Orally Disintegrating Tablets (ODT) ("Tramadol HCl ODT" or the "study drug"). The patient and the patient's partner are being asked to be in this clinical trial because they have a condition called Premature Ejaculation.

NCT ID: NCT00983151 Terminated - Clinical trials for Premature Ejaculation

Study to Evaluate Efficacy and Safety in Males Subjects With Premature Ejaculation

Start date: August 2009
Phase: Phase 3
Study type: Interventional

The purpose of this clinical trial is to test an experimental drug therapy called Tramadol Hydrochloride (HCl) Orally Disintegrating Tablets (ODT) ("Tramadol HCl ODT" or the "study drug"). The subject and his partner are being asked to be in this clinical trial because they have a condition called premature ejaculation.

NCT ID: NCT00449709 Terminated - Clinical trials for Premature Ejaculation

A Study To Assess The Pharmacokinetics Of Different Modified Release Formulations Of GSK221149 In Healthy Adult Subjects

Start date: March 2007
Phase: Phase 1
Study type: Interventional

PreTerm Labor (prior to 37 weeks gestation) is the largest single cause of infant morbidity and mortality and is frequently associated with long-term disability. Oxytocin is a hormone produced by the body during labor. GSK221149 is an experimental drug that will be used to block the effects of oxytocin, and therefore pause or prevent contractions. In this study, the pharmacokinetics of various modified release formulations of GSK221149 will be investigated in healthy non-pregnant adult subjects.