Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT03926403

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

CHU Amiens Picardie

Amiens, France, 80000

Actively Recruiting

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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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