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Fibromyalgia clinical trials

View clinical trials related to Fibromyalgia.

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NCT ID: NCT05008042 Recruiting - Fibromyalgia Clinical Trials

Evaluation of the Efficiacy of Mecobalamine in the Treatment of Long-term Pain in Women Diagnosed With Fibromyalgia

Start date: February 6, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Fibromyalgia causes long term pain where mostly women are affected. It is not entirely clear how vitamin B12 affects the human pain system, there are however many primary studies that indicate different interesting approaches. Considering that the receptor of NMDA is involved in both long-term pain and vitamin B12 deficiency its of most importance to evaluate whether vitamin B12 decreases the pain sensitivity and the experience of pain i.e hyperalgesia and allodynia, at persons with fibromyalgia.The aim of this study is therefore to evaluate the effect of Mecobalamin (vitamin B12), and describe lived experiences of pain, health, suffering and well-being in women with diagnosed fibromyalgia.

NCT ID: NCT04998630 Recruiting - Clinical trials for Myofascial Pain Syndrome

Comparison of Focused ESWT by Frequency for Patients With Myofascial Pain Syndrome

Start date: June 22, 2021
Phase: N/A
Study type: Interventional

To investigate the efficacy and safety according to the frequency of focused ESWT in patients with myofascial pain syndrome.

NCT ID: NCT04985149 Recruiting - Fibromyalgia Clinical Trials

Evaluation of the Sural Nerve With Ultrasonography and Electromyography in Patients With Fibromyalgia

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

By evaluating the ultrasonographic and electromyographic measurements of the sural nerve in patients with and without a diagnosis of fibromyalgia; to determine the relationship of these measures to each other and to the FIQ, neuropathic pain questionnaire-Clinical, single-blind, prospective, controlled study.

NCT ID: NCT04950426 Recruiting - Clinical trials for Posttraumatic Stress Disorder

Impact of Post-Traumatic Stress Disorder Treatment by Reconsolidation Therapy on Fibromyalgia Syndrome

PTSD-FMS
Start date: August 13, 2021
Phase: Phase 2
Study type: Interventional

The aim of the study is to demonstrate a significant improvement in quality of life specific to patients with fibromyalgia syndrome in patients with fibromyalgia syndrome with comorbid posttraumatic stress disorder, treated with reconsolidation blockade. Patients receive a treatment with propranolol associated with reconsolidation blockade of traumatic story once a week during 6 weeks, with evaluation at inclusion and at 3 months.

NCT ID: NCT04949100 Recruiting - Fibromyalgia Clinical Trials

Microcurrent for Fibromyalgia

Start date: October 25, 2021
Phase: N/A
Study type: Interventional

Explore the use of microcurrent therapy for fibromyalgia patients and evaluate its effect on generalized pain and quality of life. Determine if microcurrent therapy be effectively self-administered by the patient as an adjunct to medical pain management.

NCT ID: NCT04942444 Recruiting - Depression Clinical Trials

Effectiveness of Dry Needling in Fibromyalgia Patients

Start date: January 10, 2011
Phase: N/A
Study type: Interventional

Patients with fibromyalgia (FM) complain of widespread chronic pain from deep tissues including muscles. Previous research highlights the relevance of impulse input from deep tissues for clinical FM pain. Deep dry needle stimulation is an invasive treatment modality used in the management of musculoskeletal pain. Its efficacy has been confirmed in the management of myofascial trigger points, so the purpose of the study is to determine if blocking abnormal impulse input with deep dry needling stimulation of tender point may decrease hyperalgesia, clinical pain and associated symptoms such as anxiety, depression, fatigue and improve the quality of life in FM patients.

NCT ID: NCT04941118 Recruiting - Clinical trials for Efficacy of Dextrose Prolotherapy in Myofascial Pain Syndrome

Myofascial Pain Syndrome and Dextrose Prolotherapy

Start date: July 15, 2021
Phase: Phase 4
Study type: Interventional

Myofascial pain syndrome is characterized by the presence of hypersensitive points called trigger points that cause pain, tenderness, spasm, stiffness, limitation of movement, weakness, taut band within the muscle, and pain reflected by pressing in a muscle group or a single muscle. Prolotherapy is a regenerative treatment method in the treatment of chronic musculoskeletal pain, in which an irritating solution is injected, often hypertonic dextrose, into painful ligament and tendon attachments and adjacent joint spaces. In this study, it was aimed to examine the effect of prolotherapy application on pain, neck range of motion and neck disability in women with myofascial pain syndrome.

NCT ID: NCT04939922 Recruiting - Fibromyalgia Clinical Trials

China Headache Registry Study

CHRS
Start date: June 12, 2017
Phase:
Study type: Observational [Patient Registry]

In the Chinese Headache and Vertigo Registration Study, patients aged 4-99 years with headache (primary headache and secondary headache such as migraine and tension type headache), vertigo (vertigo diseases such as vestibular migraine) and chronic pain (fibromyalgia and other diseases) were collected. The biomarkers, imaging features, right-to-left shunt of the heart (lung), genetic characteristics, treatment, and outcome (in relation to other diseases) of headache-related diseases were studied, and long-term follow-up was planned.

NCT ID: NCT04938713 Recruiting - Fibromyalgia Clinical Trials

Comparison of Ketamine and Esketamine in Patients Suffering From Fibromyalgia Syndrome.

KESK-FIQ
Start date: July 1, 2021
Phase: N/A
Study type: Interventional

Ketamine and Esketamine intravenous perfusions can modulate chronic pain. The purpose of this study is to determine if Ketamine or Esketamine are favorable for outpatients suffering from fibromyalgia.

NCT ID: NCT04890964 Recruiting - Fibromyalgia Clinical Trials

Montage of HTDCS in Psycho-cognitive Functions in FM

HFTDCS
Start date: February 1, 2021
Phase: N/A
Study type: Interventional

This study aims to map the impact of anodic transcranial direct current stimulation (tDCS) for prolonged home use applied to the primary motor cortex and the left dorsolateral prefrontal córtex (DLPFC), compared to the respective treatments simulated in fibromyalgia.