Epidemiology of Chronic Pain as Part of the Post-intensive Care Syndrome
NCT ID: NCT04817696
Last Updated: 2022-02-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1079 participants
OBSERVATIONAL
2021-04-25
2022-01-25
Brief Summary
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Detailed Description
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The aim of this study is to perform a multi-center nationwide epidemiologic study of chronic pain symptoms after a critical care unit admission. The investigators intend to describe the incidence of chronic pain assessed with a Simple Verbal Score ≥ 3, 3 months after the ICU admission. The investigators also intend to describe the incidence of painful symptoms, at ICU discharge as well as the type of pain symptoms (ie neuropathic pain) at discharge and at 3 months using the ID-Pain scale. The evaluation at 3 months will be performed during a physical follow-up or self-assessed by the patient. The investigators intend to explore the risk factors associated with chronic pain, as an exploratory analysis.
The investigators are performing a nation-wide multicentric study. At this point 24 centers are participating to this study and the investigators expect to include 700 patients with a 3 months follow-up.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Patients without chronic pain symptoms
Verbal score \< 3 at 3 months
Patients with chronic pain symptoms
Verbal score ≥ 3 at 3 months
Eligibility Criteria
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Inclusion Criteria
* ICU length-of-stay ≥ 48 hours
* No major cognitive impairment that could prevent pain evaluation
Exclusion Criteria
* Patient under guardianship
* Patient unable to communicate or quantify pain with a Verbal Score and ID-Pain score
* Refusal to participate
18 Years
ALL
No
Sponsors
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Nantes University Hospital
OTHER
Responsible Party
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Locations
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CHU de Nantes
Nantes, , France
Countries
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References
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Bourdiol A, Legros V, Vardon-Bounes F, Rimmele T, Abraham P, Hoffmann C, Dahyot-Fizelier C, Jonas M, Bouju P, Cirenei C, Launey Y, Le Gac G, Boubeche S, Lamarche E, Huet O, Bezu L, Darrieussecq J, Szczot M, Delbove A, Schmitt J, Lasocki S, Auchabie J, Petit L, Kuhn-Bougouin E, Asehnoune K, Ingles H, Roquilly A, Cinotti R; ALGO-REA study group; Atlanrea Group; Societe Francaise d'Anesthesie-Reanimation-SFAR Research Network. Prevalence and risk factors of significant persistent pain symptoms after critical care illness: a prospective multicentric study. Crit Care. 2023 May 25;27(1):199. doi: 10.1186/s13054-023-04491-w.
Other Identifiers
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RC21_0020
Identifier Type: -
Identifier Source: org_study_id
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