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Myofascial Pain Syndromes clinical trials

View clinical trials related to Myofascial Pain Syndromes.

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NCT ID: NCT01203865 Recruiting - Fibromyalgia Clinical Trials

Prevalence of Fibromyalgia in Israel

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

The prevalence of fibromyalgia syndrome in the Israeli population is of importance fro planning resource allocation of medical expenditure as well as for identifying demographic and ethnic differences of this unique population compared with other western samples. In the current study the investigators aim at estimating the prevalence of fibromyalgia in this population. For this purpose a two - stage process will be used. First, a population survey will be conducted by telephone, screening for widespread pain and fatigue in the general population. This survey will use the London Fibromyalgia Epidemiology Study Screening Questionnaire. Second, a sample of patients attending the rheumatology clinic will be surveyed with this tool and will be examined in order to determine the actual proportion of patients fulfilling ACR criteria for fibromyalgia. This will enable us to calculate the positive predictive value of the London Fibromyalgia Epidemiology Study Screening Questionnaire in our population and hence to calculate the prevalence of fibromyalgia in the population.

NCT ID: NCT01189994 Recruiting - Fibromyalgia Clinical Trials

Trial of Acupuncture in the Treatment of Fibromyalgia

Start date: September 2010
Phase: N/A
Study type: Interventional

Fibromyalgia is a medical condition characterized by musculoskeletal pain, fatigue, sleep disturbances and depression. It affects population at a socioeconomically active age and represents a burden for the patients and the health care system due to its personal and functional implications. At this moment, there is no completely effective treatment for fibromyalgia, and acupuncture has been a promising alternative. This trial aims to evaluate if addition of acupuncture to standard care represents an improvement in comparison with standard care only. Thus, patients enrolled in this trial will be randomly allocated into one of two groups: group A, who besides standard treatment will receive 12 sessions of acupuncture; and group B, who will receive standard care with monthly orientation sessions for the same period. Patients will be evaluated at baseline, after completion of acupuncture treatment or orientation, and after an additional 12-week follow up. Evaluation will be based on diaries of pain and medication, and standard scales of pain, quality of life and disability.

NCT ID: NCT01151163 Recruiting - Fibromyalgia Clinical Trials

Peripheral Arterial Tonometry (PAT) Evaluation of Sleep in Fibromyalgia

Start date: January 2011
Phase: N/A
Study type: Observational

Fibromyalgia syndrome (FMS) is characterized by the presence of widespread pain, chronic fatigue and typical sleep disturbances. The purpose of the current study is to investigate the nature of sleep disturbance in FMS, using a novel technology. Peripheral arterial tonometry is a method by which peripheral arterial tone is measured non - invasively using in an ambulatory setup during sleep. The information collected reflects autonomic nervous system function and respiratory changes during sleep. We intend to utilize this technique in order to improve our understanding of the interrupted patterns of sleep in FMS and as a possible biomarker which may be used in the future to follow up FMS patients and their response to treatment.

NCT ID: NCT01149018 Recruiting - Fibromyalgia Clinical Trials

Efficacy Trial of Oral Tetrahydrocannabinol in Patients With Fibromyalgia

Start date: June 2010
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate the effectiveness of oral tetrahydrocannabinol in patients suffering from Fibromyalgia

NCT ID: NCT01026077 Recruiting - Fibromyalgia Clinical Trials

The Savella Pregnancy Registry

SPR
Start date: November 2009
Phase:
Study type: Observational [Patient Registry]

The Savella Pregnancy Registry is a US based registry designed to monitor pregnancies exposed to Savella (milnacipran HCI). This is an observational, exposure-registration and follow-up registry designed primarily to estimate the prevalence of major congenital anomalies, and secondarily to estimate the prevalence of recognized spontaneous abortions, stillbirths, induced abortions, minor congenital anomalies, and any serious adverse pregnancy outcomes among pregnancies exposed to Savella as well as adverse outcomes observed during the first year of life in off-springs born from these exposed pregnancies. Live offspring are followed from birth until age one. The Savella Pregnancy Registry is sponsored by AbbVie (formerly Actavis PLC, Forest Laboratories Inc., and Allergan) and managed by Syneos Health.

NCT ID: NCT00947622 Recruiting - Fibromyalgia Clinical Trials

Occipital Transcranial Direct Current Stimulation in Fibromyalgia

Start date: July 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to investigate whether transcranial direct current stimulation is effective in the treatment of fibromyalgia related pain. The study provides a placebo arm and the design is a cross-over design.

NCT ID: NCT00755521 Recruiting - Fibromyalgia Clinical Trials

Study Assessing the Efficacy of Etoricoxib in Female Patients With Fibromyalgia

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

The main of the proposed study is to assess whether the use of the Cox-2 inhibitor Etoricoxib is beneficial for the use in fibromyalgia. We intend to seek whether this medication may improve psychiatric and rheumatologic parameters of the disease.

NCT ID: NCT00498264 Recruiting - Fibromyalgia Clinical Trials

Effectiveness of Physical Exercise in Women With Fibromyalgia

Start date: January 2005
Phase: Phase 2
Study type: Interventional

Fibromyalgia (FMS) is a syndrome expressed by chronic widespread body pain which leads to reduced physical function and frequent use of health care services. Exercise training is commonly recommended as a treatment. The purpose of this study is to determine whether a supervised resistance muscular exercise (RME) and walking program (WP) are effective in the treatment of FMS on decrease of pain. The practical of the RME reduces the pain of participants with FMS.

NCT ID: NCT00222209 Recruiting - Fibromyalgia Clinical Trials

Clinical Study on Implicit Learning, Comorbidity and Stress Vulnerability in Chronic Functional Pain

Start date: September 2005
Phase: N/A
Study type: Interventional

The project investigates on the role of pain avoidance, comorbidity and stress response for the development of chronic somatic and visceral pain. We, the researchers at University Hospital Mannheim, assume that implicit operant learning of pain sensitization is a central mechanism of the process of pain becoming chronic, which is augmented by fear and by avoidance behaviour. Somatic and psychological comorbidity as well as stress factors are further promoting factors in chronic pain development.