Status:
COMPLETED
Interventional Study on the Impact of the Hypnosis Used as Sedation or Relaxation in the Breast Oncologic Surgery
Lead Sponsor:
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Conditions:
Breast Neoplasm
Eligibility:
FEMALE
18-100 years
Phase:
NA
Brief Summary
The aims of the study are to compare the recovering period between a group of patients with conventional sedation, a group using hypnosis as sedation during the surgery and a third group using hypnosi...
Detailed Description
Hypnosis has already demonstrated benefits among breast cancer patients undergoing oncologic surgery. Different side effects were measured during the post operative period and at each follow up visit ...
Eligibility Criteria
Inclusion
- Patient over 18 years old
- Signed informed consent form
- Patient has to be in possession of her administrative laws and affiliated to the social security insurance.
- The patient must have a diagnosis of resectable breast cancer (in situ or invasive breast cancer). . Surgical procedure must include evaluation of the axillary area (sentinel lymph node biopsy and or axillary dissection)
Exclusion
- Patient under 18 years old
- No signed informed consent form
- Patients who haven't her social security insurance and prisoners are not eligible.
- No evaluation of the axillary area.
- Breast cancer in men
Key Trial Info
Start Date :
November 15 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 31 2019
Estimated Enrollment :
284 Patients enrolled
Trial Details
Trial ID
NCT03330717
Start Date
November 15 2017
End Date
December 31 2019
Last Update
June 24 2021
Active Locations (2)
Enter a location and click search to find clinical trials sorted by distance.
1
Hôpital de Jolimont
Haine-Saint-Paul, Hainaut, Belgium, 7100
2
Cliniques Universitaires Saint-Luc
Brussels, Belgium, 1200