Actively Recruiting
Evaluation of the Relationship Between the Duration of the Evolution of the Complex Regional Pain Syndrome Type 1 (CRPS 1) and Effectiveness of the Continuous Peripheral Nerve Block (CPNB) Associated With an Intensive Rehabilitation Program
Led by Pôle Saint Hélier · Updated on 2025-04-09
30
Participants Needed
1
Research Sites
257 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study evaluates the relationship between the duration of evolution of SDRC1 and the efficacy of continuous peripheral nerve block (c-PNB) associated with an intensive rehabilitation program to improve the therapeutic strategy of SDRC1. The main hypothesis of this study is that if c-PNB is proposed earlier, the recovery, measured with a scale achievement of objectives, will be better.
CONDITIONS
Official Title
Evaluation of the Relationship Between the Duration of the Evolution of the Complex Regional Pain Syndrome Type 1 (CRPS 1) and Effectiveness of the Continuous Peripheral Nerve Block (CPNB) Associated With an Intensive Rehabilitation Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent
- Diagnosis of CRPS type 1 in an upper or lower limb according to BUDAPEST criteria
- Affiliated with a social security scheme (beneficiary or entitled person)
- Justification for Continuous Peripheral Nerve Block due to pain not responding to physical and medicinal treatments, fixed dystonia, kinesiphobia, or lack of progress in rehabilitation requiring specialized technical platform
You will not qualify if you...
- Diagnosis of CRPS Type 2
- Contraindication to analgesics used (bupivacaine, ropivacaine, levobupivacaine)
- Severe psychiatric decompensation
- Under legal protection measures
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Pôle Saint Hélier
Rennes, Brittany Region, France, 35000
Actively Recruiting
Research Team
P
Philippe Gallien, Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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