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Longitudinal Follow-up Study About Complex Regional Pain Syndrome (CRPS) Patients

NCT04703647 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 110

Last updated 2024-08-22

No results posted yet for this study

Summary

Complex regional pain syndrome (CRPS) is a post-traumatic chronic pain condition characterized by pain and other symptoms typically affecting a distal limb. Relatively little is known about the prognosis of the course of CRPS .Currently there is no specific test to diagnose CRPS.

The primary objective of the study is to investigate prospectively the evolution of CRPS and the impact of the psychosocial factors on health status, recovery, quality of life, and working status of CRPS patients.

The secondary objective of the study is to measure blood parameters in CRPS patients to investigate their evolution during the course of CRPS, and maybe to identify distinctive biomarkers associate with CRPS and that could be potential candidate for diagnosis.

Conditions

  • Complex Regional Pain Syndrome Type I

Interventions

OTHER

Administration of questionnaires for prospective group

Questionnaires: administration at T0, T1,T2,T3 and T4 of Short Form Health Survey (SF-36),Brief Pain Inventory (BPI),Disabilities of the Arm, Shoulder and Hand (DASH) for upper limb,Foot and Ankle Ability Measure (FAAM) for lower limb,Hospital Anxiety And Depression Scale (HADS),Tampa Scale of Kinesiophobia (TSK),Pain Catastrophizing Scale (PCS),Pattern Of Activity Measure - Pain (POAM-P) .

OTHER

Blood samples for prospective group

Blood samples at T0,T1,T2 and T3.

OTHER

Blood samples for control group

Blood samples just one time

Sponsors & Collaborators

  • Clinique Romande de Readaptation

    lead NETWORK

Principal Investigators

  • Bertrand Léger, PhD · institut de recherche en réadaptatation

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-14
Primary Completion
2024-12-01
Completion
2025-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04703647 on ClinicalTrials.gov