Algoneurodystrophy Clinical Trial
— ALGOSTIMOfficial title:
Comparison of the Analgesic Effect Between the Motor Cortex Stimulation (tDCS and rTMS) and the Trans-spinal Stimulation (tsDCS ) in the Algoneurodystrophy of Members. A Randomised Clinical Trial. tDCS : Transcranial Direct-current Stimulation rTMS : Repetitive Transcranial Magnetic Stimulation tsDCS : Transcutaneous Spinal Direct Current Stimulation
Verified date | May 2022 |
Source | University Hospital, Grenoble |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
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.
Status | Completed |
Enrollment | 36 |
Est. completion date | February 22, 2022 |
Est. primary completion date | June 11, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Patient's written consent - Patient suffering from an algoneurodystrophy for more than a year. - Diagnosis of algoneurodystrophy confirmed by an osseous scintigraphy - Stable treatment for at least 1 month - Patient non-responsive to pharmacological treatments - VNS > 3 at the time of screening Exclusion Criteria: - Drug addiction - History of epilepsy, head trauma, Psychiatric pathology likely to hamper the progress of the study. - Intracranial ferromagnetic material or an implanted stimulator - MRI contraindication - Algoneurodystrophy due to a nervous lesion - Pregnant women, parturient women, breast-feeding mother. Lack of effective contraception |
Country | Name | City | State |
---|---|---|---|
France | Service de Physiologie - Explorations Fonctionnelles, Hôpital Henri Mondor | Créteil | Ile De France |
France | Centre de la douleur, CHU Grenoble Alpes | Grenoble | Isere |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Grenoble |
France,
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* Note: There are 41 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Visual numeric scale of pain between the three groups | Baseline to 1 month | ||
Secondary | The Clinical Global Impression scale (CGI) between the three groups | Baseline, 3 months after the beginning of the treatment (day 90), and 1 month after the end of the treatment (Day 180) | ||
Secondary | The SF12 quality of life questionnaire between the three groups | Baseline, 3 months after the beginning of the treatment (day 90), and 1 month after the end of the treatment (Day 180) | ||
Secondary | The Hospital Anxiety and Depression scale (HAD) between the three groups | Baseline, 3 months after the beginning of the treatment (day 90), and 1 month after the end of the treatment (Day 180) | ||
Secondary | The Neuropathic Pain Symptom Inventory scale (NPSI) between the three groups | Baseline, 3 months after the beginning of the treatment (day 90), and 1 month after the end of the treatment (Day 180) | ||
Secondary | Evolution of the conductance of feet and hands by using Sudoscan | The body conductance will be used to assess the evolution of the Impact of the neurostimulation on the sympathetic nervous system and on the small fiber neuropathy. | Baseline, 3 months after the beginning of the treatment (day 90), and 1 month after the end of the treatment (Day 180) | |
Secondary | Modifications of the sensori-motor cortical cards by using a MRI | Baseline, and 1 month after the end of the treatment (Day 180) |