Status:
COMPLETED
Effectiveness of Energy Resonance by Skin Stimulation in the Management of Anxious Patients Who Require Scheduled Orthopaedic Surgery
Lead Sponsor:
Centre Hospitalier Universitaire Dijon
Conditions:
Patient Requiring Scheduled Conventional Orthopedic Surgical Intervention of the Upper or Lower Limb
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
The need for a surgical procedure may cause a patient to experience reactive anxiety. This reaction is appropriate if it is of low to moderate intensity. On the other hand, various studies have shown ...
Eligibility Criteria
Inclusion
- Patient who has given oral consent
- Adult patient requiring scheduled conventional orthopedic surgery of the upper limb (wrist, elbow, shoulder) or lower limb (ankle, foot, knee, hip)
Exclusion
- Patient not affiliated to a national health insurance system,
- Patient subject to a legal protection measure (curatorship, guardianship)
- Patient subject to a justice protection measure
- Pregnant, parturient or breastfeeding woman
- Patient unable to give consent
- Minor
- Patient with a pace maker
- Patient with cognitive problems: Alzheimer's, senile dementia
- Patient who has already received ERCS as part of surgery
- Patient who does not speak or understand French
- Patient with psychiatric disorders: major depression, bipolar disorder, addictive disorders, psychotic disorders (psychosis, schizophrenia, acute delirium)
Key Trial Info
Start Date :
April 5 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 12 2023
Estimated Enrollment :
86 Patients enrolled
Trial Details
Trial ID
NCT03773198
Start Date
April 5 2019
End Date
May 12 2023
Last Update
December 7 2023
Active Locations (1)
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1
Chu Dijon Bourogne
Dijon, France, 21000