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Active clinical trials for "Myofascial Pain Syndromes"

Results 651-660 of 1012

Study to Evaluate the Efficacy of Botulinum Toxin Serotype A Injections for Cervicobrachial Myofascial...

Cervicobrachial NeuralgiaMyofascial Pain Syndromes

Several studies have previously examined the use of botulinum toxin serotype A for myofascial pain of the neck and shoulders (cervicobrachial syndrome). These studies have suffered from: inclusion of confounding conditions in the proband group, and inability to identify predictors of response. This study attempts to define the characteristics of responders to botulinum serotype A for myofascial pain of the neck and shoulders (cervicobrachial syndrome).

Completed14 enrollment criteria

Effects of Myofascial Induction Therapy on Pressure Pain and Ankle Range of Motion.

FasciaTrigger Point Pain3 more

In this study, it will be assessed if there are changes in ankle dorsiflexion and pressure pain after performing the myofascial induction technique in the calf.

Completed6 enrollment criteria

Fibromyalgia: Interventions for Pain and Mood Regulation

Fibromyalgia

This study compares the impact of cognitive-behavioral therapy for pain (CBT-P), mindful awareness and acceptance treatment (M), and arthritis education as an active control condition (E) on mental and physical health outcomes among adults with chronic pain due to fibromyalgia (FM).

Completed6 enrollment criteria

Prospective Evaluation of Reduced Impedance Noninvasive Cortical Electrostimulation (RINCE) to Reduce...

Fibromyalgia

The purpose of this open label study is to provide up to 24 active treatments of noninvasive cortical electrostimulation therapy only to those fibromyalgia patients who experienced inadequate pain reduction in a sham controlled double blinded lead in study, NPT-201 (NCT01825954). The therapy will be provided by the NeuroPoint device using the same protocol as that used in active treatment arms of NPT-201. The study's primary outcome measure will be the patient's change from baseline in self-reported 24-hour average pain intensity. The study will provide active treatment to those participants who received sham therapy in NPT-201, and will test whether or not additional therapy applications might further improve pain in those participants who previously received active therapy, but did not achieve adequate pain relief.

Completed11 enrollment criteria

Benefits of Dry Needling in Trigger Points on Autonomic Nervous System and Corporal Composition...

FibromyalgiaTrigger Points

This study evaluates the benefits of dry needling in trigger points on autonomic nervous system, photoelectric plethysmography, body composition in patients with fibromyalgia syndrome.

Completed15 enrollment criteria

TD-9855 Mass Balance Study

ADHDFibromyalgia

The purpose of the study is to evaluate the absorption, distribution, metabolism, and excretion (ADME) of a single oral dose of [14C]TD-9855

Completed7 enrollment criteria

Changes on Pain and Range of Motion by the Use of Kinesio Taping in Subjects With Myofascial Trigger...

Mobility LimitationMyofascial Trigger Point Pain

The aim of this study is to demonstrate that the application of Kinesio Taping on a myofascial trigger point in the trapezius muscle able to cause a decrease of the trigger point pain and an increase of the cervical range of motion in asymptomatic subjects

Completed13 enrollment criteria

Serious Game for Fibromyalgia Patients

Fibromyalgia

Aim: To check the applicability of LitEmotion© in people with Fibromyalgia. Design: randomized clinical trial, with pre, post and follow-up evaluation. Researchers and outcome evaluator blinded. Method: The experimental group will play during three weeks to LitEmotion© videogame. The control group will not play.

Completed3 enrollment criteria

Treatment of CFS & Fibromyalgia With Recovery Factors

FibromyalgiaChronic Fatigue Syndrome

The study will explore if Recovery Factors improve symptoms in fibromyalgia and chronic fatigue syndrome

Completed3 enrollment criteria

Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia

Fibromyalgia

The study is designed as a prospective, randomized, double-blind, single center study with a 6 month duration post permanent system implantation. Forty patients will be implanted. During trial stimulation, patients will be randomized into one of two study arms for two weeks. Crossover will occur at the 2 week study visit to the opposite group. After completion of these two arms, every patient will subsequently complete participation in the third study arm. After completion of the third arm, patients will be evaluated to determine if they are a positive responder responder. If so, the patient will have the option of obtaining the permanent implant.

Completed18 enrollment criteria
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