Could a day hospital visit ease chronic pain?
NCT ID NCT04913051
First seen Jul 01, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This trial investigates whether a multidisciplinary day hospital program can improve quality of life for adults with chronic regional pain syndrome (CRPS), a painful condition that affects movement and daily function. Participants receive coordinated care from a team of specialists in a single day. The study measures changes in pain, limb function, and overall well-being using standard questionnaires.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- multidisciplinary day hospital program
- What this could lead to
- If effective, this approach could offer a structured, non-drug way to improve daily life and reduce pain for people with CRPS.
- What could go wrong
- This is a small, early-stage study with only 36 participants, so results may not apply to everyone. The program may not provide lasting benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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36 people
The number who actually took part.
- Started
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Jun 2021
- Finished
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Oct 2022
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with Chronic Regional Pain Syndrome referred to the Chronic Pain Facility for the first time
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient volunteers over 18 years of age * Diagnosis of CRPS according to the Budapest criteria * Referred to pain assessment and treatment center Exclusion Criteria: * Patients unable to express their wishes or understand the protocol * Diagnosis of CRPS not meeting Budapest criteria * Patients previously seen at pain assessment and treatment center for the care of CRPS
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre Hospitalier Du Mans
Le Mans, 72000, France