Clinical trial Recruiting at 1 site Interventional Ages 18 and up

tDCS for CRPS: see if a non‑invasive brain stimulation helps reduce pain

Official title: Study of the Effectiveness of Transcranial Direct Current Stimulation (tDCS) in the Management of Complex Regional Pain Syndrome

Run by Polyclinique de l'Europe · NCT07361692 · Data updated 2026-11-12

This trial tests whether transcranial direct current stimulation can lessen pain and improve mood and function for people with complex regional pain syndrome.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment32 (estimated)
SponsorPolyclinique de l'Europe
Academic / other
Locations1 site (Saint-Nazaire)
StatusRecruiting
StartedApril 1, 2026
Main results expectedJune 1, 2027
Study endsJune 2027
Registry record updatedJune 18, 2026
Trial IDNCT07361692 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with active CRPS meeting Budapest criteria, confirmed by scintigraphy, and who are affiliated with a social security scheme.

Probably not a fit

Patients who do not respond to tDCS or who experience no meaningful pain reduction may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will compare a real tDCS treatment to a sham control in CRPS patients over one month of treatment and one month afterward. They will measure pain levels, anxiety and depression, functional impact of pain, central sensitization, and record any adverse effects. The study uses a non-invasive, low-risk stimulation approach already explored in other chronic pain conditions. Outcomes will indicate if tDCS provides meaningful relief beyond placebo. The trial is conducted at Polyclinique de l'Europe in Saint-Nazaire and targets adults with active CRPS who meet Budapest criteria.

Why it matters

Potential benefit: If successful, participants may experience reduced pain and improved quality of life and functioning.

How similar studies have gone: Previous studies in other chronic pain conditions suggest tDCS can be beneficial; applicability to CRPS is being explored.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Major
* Clinically active or active complex regional pain syndrome (CRPS) with positive Budapest criteria
* Scintigraphy showing signs consistent with CRPS
* Being affiliated with or a beneficiary of a social security scheme

Exclusion Criteria:

* Algodystrophy no longer meeting the Budapest criteria
* Relative contraindication to tDCS: psychosis (including treated psychosis), uncontrolled epilepsy, large scalp scar, intracerebral/intracranial metallic body
* Pregnant or breastfeeding women
* Minors
* Persons under legal protection (guardianship, conservatorship, and protective supervision)
* Persons deprived of their liberty by judicial or administrative order
* Unwilling individuals who cannot give their consent or cannot return for scheduled visits according to the protocol

Where it's running

  • Polyclinique de l'Europe
    Saint-Nazaire, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.