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Somatoform Disorders clinical trials

View clinical trials related to Somatoform Disorders.

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NCT ID: NCT00377468 Recruiting - Clinical trials for Complex Regional Pain Syndromes

Effect of Delta-9-Tetrahydrocannabinol on the Prevention of Chronic Pain in Patients With Acute CRPS (ETIC-Study)

Start date: September 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether application of low dose Delta9-Tetrahydrocannabinol can prevent the development of chronic pain in patients with acute CRPS.

NCT ID: NCT00371033 Active, not recruiting - Clinical trials for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

Efficacy & Safety Study of Pregabalin to Treat Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

CPCRN RCT#2
Start date: March 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether pregabalin is an effective treatment for Chronic Prostatitis/Chronic Pelvic Pain Syndrome.

NCT ID: NCT00368212 Completed - Clinical trials for Somatoform Disorders

Integrated Treatment Program for Hypochondriasis in Primary Care Settings

Start date: May 2005
Phase: Phase 3
Study type: Interventional

This study will evaluate the effectiveness of an integrated three-part treatment program in improving the quality of care and treatment outcomes of people with hypochondriasis in primary care settings.

NCT ID: NCT00276887 Completed - Clinical trials for Somatoform Disorders

Cognitive Behavior Therapy for Somatization Disorder

Start date: September 1999
Phase: Phase 2
Study type: Interventional

This study will examine the long-term effects of cognitive behavioral therapy on the physical symptoms, functioning, and health care utilization of people with multiple medically unexplained physical symptoms.

NCT ID: NCT00246142 Completed - Clinical trials for Myofascial Pain Syndromes

A Study of the Combination of Electrical Stimulation and Dysport® in Myofascial Pain Syndrome.

Start date: April 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether electrical stimulation enhances the effect of botulinum toxin type A (Dysport®) on myofascial pain syndrome.

NCT ID: NCT00217243 Completed - Clinical trials for Complex Regional Pain Syndromes

Evoked Fields After Median and Ulnar Stimulation

Start date: June 2005
Phase: N/A
Study type: Observational

In order to be able to study the effects of evoked fields with magnetoencephalography (MEG) in two groups of patients, comparison is made with a group of healthy volunteers.

NCT ID: NCT00194623 Terminated - Clinical trials for Chronic Male Pelvic Pain Syndrome

Botox as a Treatment for Chronic Male Pelvic Pain Syndrome

Start date: August 2003
Phase: Phase 4
Study type: Interventional

Chronic pelvic pain syndrome (CPPS) is thought to affect approximately 8% of men aged 18 and older. Patients with this condition experience pain in the perineum, the genitalia, and the rectum. As well, there is associated voiding, sexual, and ejaculatory dysfunction. The impact of patient well-being is thought to be equivalent to patients with congestive heart failure. The etiology of this condition is unknown, thus making treatment very difficult. Researchers have pursued an infectious cause for the disease; however, studies have failed to substantiate this theory. Despite this, the main treatment offered to patients is long-term antibiotic therapy. Results from this treatment modality have been unsatisfactory. Other groups have postulated that the symptoms of CPPS may be secondary to neuromuscular factors. Some studies have demonstrated increases in pelvic muscular tone. Maneuvers such as prostate massage and levator massage have shown some benefit in relieving symptoms. Treatment with alpha-blockers to relax prostate smooth muscle has brought about improvement in a portion of patients. Use of generalized muscle relaxants has produced mediocre results. However, many of these neuromuscular treatments are generalized and do not target the perineal musculature directly. It is theorized that spasm of the perineal muscles triggered by an unknown noxious stimuli (e.g. infection) cause the pain and symptoms of CPPS. At our center, we have performed pilot studies using botulinum toxin A. Four patients were treated with Botox". 100 U were injected in three locations in the midline of the bulbocavernosus muscle. The bulbocavernosus muscle is easily accessible and shares innervation with the pelvic musculature. Patient's response to medication was measured by the NIH Prostatitis pain scale and as well as the University of Washington prostatitis pain scale. All patients reported resolution of symptoms. Remission lasted for duration of 10-12 weeks. No patients reported adverse events. HYPOTHESIS Botulinum toxin A is effective in the treatment of chronic pelvic pain syndrome in men.

NCT ID: NCT00166452 Completed - Clinical trials for Complex Regional Pain Syndrome, Type 1

A Study of the Effect of Lenalidamide on Complex Regional Pain Syndrome Type 1

Start date: July 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if lenalidomide is a safe and effective treatment for complex regional pain syndrome type 1 (CRPS).

NCT ID: NCT00149799 Completed - Anxiety Disorders Clinical Trials

Effectiveness of Escitalopram in the Treatment of Body Dysmorphic Disorder

Start date: May 2005
Phase: Phase 3
Study type: Interventional

This study's primary aim is to compare time to relapse and relapse rates in responders to acute escitalopram who are then randomized to placebo versus continuation treatment with escitalopram.

NCT ID: NCT00149760 Completed - Clinical trials for Somatization Disorder

Effectiveness of Cognitive-Affective Behavior Therapy for the Treatment of Somatization Disorder

Start date: August 2003
Phase: Phase 2
Study type: Interventional

This study will examine the long-term effect of cognitive-affective behavior therapy on the physical symptoms, functioning, and health care utilization of people with somatization disorder.