Actively Recruiting
Evaluation of the Effectiveness of Hypnosis Support on Patient Perception of Outpatient Surgery Under Local Anaesthesia
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2026-05-13
66
Participants Needed
1
Research Sites
400 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Many clinical trials assessing the effectiveness of hypnosis have been conducted in recent years, some of which show that hypnosis reduces pain perception better than drug treatments administered to control groups, and that it is at least as effective as other complementary therapies (such as massage, acupuncture, yoga). However, their conclusions are limited by a significant risk of bias, and further studies with rigorous methodology remain necessary. The hypothesis of this study is that hypnosis support methods can reduce anxiety in patients requiring facial surgery under local anaesthesia, and thus improve their medical management. The purpose of this study is to evaluate the effectiveness of hypnosis support on the patient's state of anxiety before and after outpatient surgery under local anaesthesia in the Maxillofacial Surgery Department.
CONDITIONS
Official Title
Evaluation of the Effectiveness of Hypnosis Support on Patient Perception of Outpatient Surgery Under Local Anaesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient treated under local anaesthesia in the Maxillo Facial Surgery department with ultra-short circuit
- Patient undergoing face surgery
- Patient who has received appropriate information and has provided informed consent
- Adult patient 9 18 years old
- Patient with a score of 9 36 on the initial anxiety self-assessment questionnaire
You will not qualify if you...
- Patient under general anaesthesia
- Patients treated in conventional inpatient care or in the traditional ambulatory circuit
- Patient under guardianship or trusteeship
- Minor patient < 18 years of age
- Patient who has not provided informed consent or who cannot submit to the study protocol
- Patient suffering from cognitive disorders (ex: Alzheimer's disease)
- Patients who are deaf or hearing-impaired
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Amiens Picardie
Amiens, France, 80000
Actively Recruiting
Research Team
M
Martine Gosset, ORN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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