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Pelvic Pain clinical trials

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NCT ID: NCT00672087 Completed - Clinical trials for Painful Bladder Syndrome

Diagnostic Challenges in IC (and Male CPPS)

Start date: September 2003
Phase:
Study type: Observational

The etiology and pathogenesis of interstitial cystitis (IC) and its related condition in men, chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) has remained elusive. This has hampered development of mechanistic treatment strategies for these common, chronic and distressing medical conditions. We believe that IC and perhaps CP/CPPS are a spectrum of complex but inter-related genetic and acquired diseases resulting from the interaction of several genes regulating immune/inflammatory and neurogenic parameters and environmental factors/circumstances or exposure, culminating in the combination of pain, frequency, urgency and sexual specific symptoms. New research has delineated the dynamic and powerful association of the immune and neurogenic system in pain activation. An immune-modulated neurogenic model of IC illuminating the action of immune derived substances and pain related substances might be important in discovering the determinants of pain, voiding dysfunction and gender specific sexual problems. This inter-related dynamic model of IC disease pathogenesis could be explored for potential avenues leading to novel diagnostic and treatment strategies. We plan to identify and evaluate the sensitivity and specificity of several novel nerve and inflammation related markers in the diagnosis and follow up of IC (and CP/CPPS). By correlating the levels of urine immune and pain related substances to disease mechanisms, severity and progression, we may be able to create a human disease specific model for diagnosis and treatment.

NCT ID: NCT00590811 Completed - Pelvic Pain Clinical Trials

Prevalence of Menstrual Cycle Related Pain Complains in Adolescents and Young Adults

Start date: January 2008
Phase: N/A
Study type: Observational

The aim of this study is to determine the prevalence of menstrual cycle related pain complains in adolescents and young adults.

NCT ID: NCT00554320 Completed - Fibromyalgia Clinical Trials

Effect of Repetitive Transcranial Direct Current Stimulation (tDCS) on Chronic Pelvic Pain

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

We will rigorously test whether modulation of the motor cortex by transcranial direct current stimulation (tDCS) is an effective treatment for patients with chronic pelvic pain through the following specific aims: A) The primary aim of this study is to determine whether transcranial direct current stimulation applied to the motor cortex in patients with chronic pelvic pain induces a significant decrease in the pain or symptoms as compared with sham tDCS. We will also measure changes in the clinical symptom scores of multiple pelvic organs, drug intake (narcotic), anxiety, depression, traumatic stress, as well as overall improvement in the quality of life to assess the effects of this treatment. B) Determine the duration of the clinical effects of tDCS. We will therefore compare the amelioration of pain and related symptoms between active and sham tDCS for one year following treatment. C) Determine whether tDCS changes the threshold for pain detection as compared with sham tDCS. Patients with chronic pelvic pain have a lower threshold for pain as compared to healthy subjects and we hypothesized that this threshold will increase after stimulation with tDCS. D) Finally, we will examine whether 5 days of tDCS treatment is safe for use in chronic pelvic pain patients. Safety will be assessed through neuropsychological tests and adverse event reporting.

NCT ID: NCT00475189 Completed - Pelvic Pain Clinical Trials

Study of Loestrin 24(24 Days of "Real" Pills) Fe Versus Loestrin 1/20 (21 "Real" Pills)

Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of this research study is to assess hormone withdrawal symptoms in women while taking an oral contraceptive in the novel 24/4 (24 days of "real" pills) manner in comparison to taking pills in the standard 21/7 (21 "real" pills) manner. It is hypothesized that the 24/4 method will reduce common hormone withdrawal symptoms compared to the standard 21/7 regimen. It is further hypothesized that women using the 24/4 regimen will report greater satisfaction scores.

NCT ID: NCT00455845 Completed - Endometriosis Clinical Trials

The Effectiveness of Lng IUD for Treatment of the Patient Undergone Conservative Surgery for Pelvic Endometriosis

Start date: April 2007
Phase: Phase 3
Study type: Interventional

this study is to determine whether the frequency and severity of pelvic pain or dysmenorrhea are reduced in women with symptomatic endometriosis in whom a Lng IUD is inserted after operative laparoscopy compare with those treated with laparoscopic surgery only

NCT ID: NCT00444730 Completed - Prostate Cancer Clinical Trials

Urology Database for Outcomes Research

Start date: January 2007
Phase: N/A
Study type: Observational

The purpose of initiating the urology database is to collect relevant retrospective data via chart review related to patients undergoing radical prostatectomy via the retropubic, perineal, laparoscopic, and robotic assisted laparoscopic approaches and InterStim implantation. This data will be utilized to evaluate the health benefits and outcomes of each of these procedures to enhance care and treatment.

NCT ID: NCT00440505 Completed - Pelvic Pain Clinical Trials

Effect of Nicotine on Chronic Pelvic Pain

Start date: February 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test whether transdermal nicotine reduces pain among women with chronic pelvic pain.

NCT ID: NCT00434343 Completed - Clinical trials for Interstitial Cystitis

Physical Therapy Trial for Pelvic Pain

UPPCRN-RCT#1
Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a randomized trial of physical therapy for pelvic pain is feasible.

NCT ID: NCT00420550 Completed - Pelvic Pain Clinical Trials

Study of Biomarkers and the Relaxation Response Using Guided Imagery in Women With IC

Start date: January 2007
Phase: Phase 2
Study type: Interventional

Interstitial cystitis (IC) affects more than one million women in the United States. It has been thought that IC patients who have been unable to obtain adequate relief from medical remedies would value a psychotherapeutic intervention that could diminish some of their pain. There are currently no studies using biomarkers with the use of a relaxation technique called guided imagery in IC patients. Many guided imagery intervention studies in areas such as cancer, post-operative pain, and arthritis reported that guided imagery resulted in improvements in the psychological or physiological outcomes examined. If this is also true in IC patients, this intervention may prevent the use of unnecessary medications and procedures that are currently being used.

NCT ID: NCT00379002 Completed - Sexual Dysfunction Clinical Trials

The Women's Urology Center/WISH Database Project

Start date: July 2006
Phase:
Study type: Observational

Comprehensive database from the Women's Urology Center/WISH (Women's Initiative for Pelvic Pain and Sexual Health) program at Beaumont.