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Sexual Dysfunction clinical trials

View clinical trials related to Sexual Dysfunction.

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NCT ID: NCT01312259 Recruiting - Sexual Dysfunction Clinical Trials

Clinical Efficacy of Changing the InterStim® Parameters in Patients With Interstitial Cystitis/Painful Bladder Syndrome

Start date: April 2011
Phase: Phase 4
Study type: Interventional

Purpose: 1. To demonstrate better symptoms control (pain, urinary urgency and frequency) with sacral neuromodulation (SNM) in patients with interstitial cystitis /painful bladder syndrome (IC/PBS) using a stimulation frequency of 40 hertz (experimental) compared to a frequency of 14 hertz (standard). 2. The evaluate the efficacy of the two frequency settings on the other associated conditions that often coexist in patients with IC/PBS, such as female sexual dysfunction (FSD), bowel dysfunction, high tone pelvic floor dysfunction (HTPFD, painful spasm of the pelvic floor muscles), Vulvodynia (pain at the opening of the vagina).

NCT ID: NCT01252576 Active, not recruiting - Sexual Dysfunction Clinical Trials

Linguistic and Cultural Validation in Italian of Female Sexual Function Index (FSFI) Questionnaire

Start date: December 2010
Phase: N/A
Study type: Observational

300 italian women will be enroll for linguistic and cultural validation in italian of Female sexual function index (FSFI). This questionnaire is used in most countries to investigate female sexual function. To date there are not validate questionnaires in italian on female sexual function. We decided to start the validation process to give a validated tool to italian investigators.

NCT ID: NCT01238705 Recruiting - Hypertension Clinical Trials

Combined Antihypertensive Therapy and Sexual Dysfunction

Start date: April 2008
Phase: Phase 4
Study type: Interventional

This randomized,active controlled study aimed to compare the effects on sexual function of treatment with combined antihypertensive drugs. The researchers hypothesize that: 1. Both felodipine-irbesartan combination and felodipine-metoprolol combination are effective in lowing blood pressure in patients with essential hypertension. 2. Felodipine-metoprolol combination induces a worse sexual function and a reduction of sex hormone,whereas felodipine-irbesartan combination does not impair sexual function and does not change hormone levels. 3. Oxidative stress decline after both combination regimens. Felodipine-irbesartan combination has a greater impact on oxidative stress indicators than felodipine-metoprolol combination.

NCT ID: NCT01230762 Completed - Clinical trials for Erectile Dysfunction

An Open-Label Study of the Long-Term Safety of Dapoxetine HCl in the Treatment of Rapid Ejaculation

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the long-term safety of dapoxetine in men with rapid ejaculation.

NCT ID: NCT01189825 Completed - Sexual Dysfunction Clinical Trials

Efficacy of Exercise for Sexual Side Effects of Antidepressants

Start date: June 2009
Phase: N/A
Study type: Interventional

The major aim of the this study is to replicate findings of previous research that examined the effects of acute exercise on sexual arousal in women in a novel population, namely, women taking antidepressants of the selective serotonin reuptake inhibitors (SSRI) or selective serotonin and norepinephrine reuptake inhibitors (SNRI) class. In previous studies it has been found that acute, moderate-intensity exercise facilitated physiological sexual arousal responses in healthy, sexually functional women. However, it is known that antidepressants may induce sexual dysfunction, and thus in the present study, the investigators are examining whether acute exercise may facilitate sexual responses in women with taking antidepressants, including women with antidepressant-related sexual dysfunction.

NCT ID: NCT01159678 Completed - Sexual Dysfunction Clinical Trials

Online Psychoeducation for Sexual Dysfunction in Cancer Survivors

OPES
Start date: October 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to test an online psychoeducational intervention for men and women with sexual difficulties after surgery for colorectal (men and women) or gynecological (women only) cancer. A psychoeducational intervention is a brief, educational treatment that encourages participants to also pay attention to, and modify, their thoughts, feelings, and behaviour.

NCT ID: NCT01097980 Completed - Sexual Dysfunction Clinical Trials

Trazodone for SSRI-sexual Dsyfunction

T-SSRI-SD
Start date: April 2010
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the efficacy of trazodone in the treatment of selective serotonin reuptake inhibitor(s) associated sexual dysfunction. The secondary domains assessed were the relationship between 5-HT2A polymorphism and treatment efficacy.

NCT ID: NCT01086007 Completed - Sexual Dysfunction Clinical Trials

Pain Related Sexual Dysfunction After Laparoscopic Inguinal Hernia Repair

Start date: February 2010
Phase: N/A
Study type: Observational

Previous studies have reported that about 3 % of patients who have had open inguinal herniorrhaphy had a visceral, ejaculatory-related pain. The investigators want to assess this problem among patients after laparoscopic inguinal hernia repair with(self-administered questionnaire study).

NCT ID: NCT01063855 Completed - Clinical trials for Erectile Dysfunction

Concomitant Use of PriLigy in Men Treated for Erectile Dysfunction

COUPLE
Start date: April 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of dapoxetine compared to placebo in men with premature ejaculation and erectile dysfunction who are currently being treated with a phosphodiesterase-5 inhibitor (ie, sildenafil, vardenafil, or tadalafil) for erectile dysfunction.

NCT ID: NCT00988130 Recruiting - Prostate Cancer Clinical Trials

High-Intensity Focused Ultrasound Focal Ablation in Treating Patients With Progressive Prostate Cancer

Start date: July 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: High-intensity focused ultrasound focal ablation uses high-energy sound waves to kill tumor cells. PURPOSE: This phase II trial is studying the side effects of high-intensity focused ultrasound focal ablation and to see how well it works in treating patients with progressive prostate cancer.