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Complex Regional Pain Syndromes clinical trials

View clinical trials related to Complex Regional Pain Syndromes.

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NCT ID: NCT03203772 Completed - Neuropathic Pain Clinical Trials

Immersive Virtual Reality for Neuropathic Pain

Start date: August 14, 2016
Phase: N/A
Study type: Interventional

Investigating how neuropathic limb pain, including phantom limb pain or complex regional pain syndrome, is affected by virtual reality. While several studies have looked into virtual reality for treating this type of pain, few have used the latest immersive virtual reality hardware combined with motion control for an engaging virtual mirror therapy experience. The investigators are interested in studying the use of virtual reality as an alternative treatment option for these conditions.

NCT ID: NCT03174249 Completed - Clinical trials for Complex Regional Pain Syndromes

Exposure Therapy Combined With Cortical Interventions for CRPS-II

ETHICS
Start date: September 1, 2012
Phase: N/A
Study type: Interventional

Consecutive patients with long-standing complex regional pain syndrome II in a lower limb are treated with graded exposure therapy in vivo in combination with methods targeting cortical reorganisation.

NCT ID: NCT03111225 Completed - Clinical trials for Complex Regional Pain Syndromes

Thoracic Paraspinal Soft Tissue Mobilizations in Treatment of Patients With Upper Limb Complex Regional Pain Syndrome

Start date: June 6, 2016
Phase: N/A
Study type: Interventional

This study examines the prevalence of trigger points in muscles in the thorax in upper limb Complex Regional Pain Syndrome (CRPS) patients, compared to healthy subjects. In addition, we will examine if adding treatment to muscles in the thoracic area (to the regular physical therapy treatment) will alleviate some of the sensitivity in the upper limb in CRPS patients.

NCT ID: NCT02972359 Completed - Clinical trials for Complex Regional Pain Syndrome

Safety of Intravenous Neridronic Acid in CRPS

Start date: December 20, 2016
Phase: Phase 3
Study type: Interventional

The aim of this trial was to investigate the safety of intravenous neridronic acid in patients with complex regional pain syndrome (CRPS). The trial was divided into 3 periods: a 60-day enrollment period, a treatment period consisting of 4 infusions over 10 days, and a follow-up period of approximately 50 weeks (with visits at Week 2, Week 6, Week 12, Week 26, Week 39, and Week 52).

NCT ID: NCT02912975 Completed - Phantom Limb Pain Clinical Trials

A Clinical Trial of Mirror Treatment for Phantom Pain

Start date: March 2016
Phase: N/A
Study type: Interventional

A randomized controlled clinical to examine the effect of mirror therapy on phantom pain and residual limb pain in patients with traumatic transtibial amputations in Cambodia. The study will be conducted with a semi-crossover design using self-rated pain and function as the main result variables.

NCT ID: NCT02901002 Completed - Clinical trials for Complex Regional Pain Syndromes

Body Perception and Complex Regional Pain Syndrome

SDRC
Start date: January 6, 2017
Phase: N/A
Study type: Observational

In CRPS, perturbation of body image and pseudo-neglect syndrome of the body part affected are frequently found. Pain and sensory perturbation seems to modify the way patients perceived their body part affected. Does a local body image perturbation can affect the balanced of the global self-awareness?

NCT ID: NCT02837822 Completed - Chronic Pain Clinical Trials

Effects of Spinal Cord Stimulation on Sensory Perceptions of Chronic Pain Patients

Start date: October 2015
Phase: N/A
Study type: Interventional

It's well known that Spinal cord stimulation (SCS) changes the perception of chronic pain in the area stimulated by epidural electrodes. However, we don't know the effect of this type of stimulation on the perception of external sensations (temperature, touch, pressure, and vibration) and sharp pain. Quantitative sensory testing (QST) is used to quantify somatosensory phenotype. This QST battery tests different subtypes of nerve fibres (Aβ, Aδ and C) involved in the transduction of sensory information from the periphery to the spinal cord. The purpose of this study is to evaluate the effects of the SCS on sensory perceptions of patients with chronic pain (CRPS, FBSS). Sensorial perception tests will be carried out in accordance with a standardized procedure (Rolke et al. Pain, 2006). For non-implanted patients, an initial visit will be conducted before the operation. For all participants, two other visits will take place at least 6 months after the operation to perform the tests with and without stimulation.

NCT ID: NCT02817880 Completed - Algoneurodystrophy Clinical Trials

Comparison of the Analgesic Effect Between the Motor Cortex Stimulation and the Trans-spinal Stimulation in the Algoneurodystrophy.

ALGOSTIM
Start date: July 25, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the analgesic effectiveness of two motor cortex neurostimulations (tDCS and rTMS) and the trans-spinal neurostimulation (tsDCS ) in the algoneurodystrophy.

NCT ID: NCT02753101 Completed - Sciatica Clinical Trials

[18F]FTC-146 PET/MRI in Healthy Volunteers and in CRPS and Sciatica

Start date: February 9, 2016
Phase: Early Phase 1
Study type: Interventional

Chronic pain can result from injured or inflamed nerves, as occurs in people suffering from sciatica and CRPS. These nerve injuries or regions of nerve irritation are often the cause of pain in these conditions, but the current diagnostic tools are limited in pinpointing the area of origin. Several studies have implicated involvement of sigma-1 receptors in the generation and perpetuation of chronic pain conditions, others are investigating anti sigma-1 receptor drugs for the treatment of chronic pain. Using the sigma-1 receptor (S1R) detector and experimental radiotracer [18F]FTC-146 and positron emission tomography/magnetic resonance imaging (PET/MRI) scanner, the researchers may potentially identify the source of pain generation in patients suffering from complex regional pain syndrome (CRPS) and chronic sciatica. The ultimate goal is to assist in the optimization of pain treatment regimens using an [18F]FTC-146 PET/MRI scan. The study is not designed to induce any physiological/pharmacological effect.

NCT ID: NCT02663284 Completed - Clinical trials for Complex Regional Pain Syndrome

Evaluation of the Physiodoloris Pain Monitor in Patients With Complex Regional Pain Syndrome

ANI-ALGO
Start date: April 2012
Phase: N/A
Study type: Interventional

A French University team (M. Jeanne, MD, and M. LOGIER, Ph D) have developed a pain assessment tool based on the analysis of the variability heart rate which evaluates the Analgesia Nociception Index (ANI). This index is intended to give a quantification of pain. The aim of the present study is to assess the validity of the ANI parameter in patients with Complex Regional Pain Syndrome treated with a nerve block (reversible pain).