Breast Neoplasm
Conditions
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 hypnosis as a relaxation method and preparation but enjoying a classic sedation for their surgery. Comparaison of pain ( different types of pain), consumption of pain killers ,anxiety and fatigue on day0,1, 8 after surgery and every. 3 months during the first 2 years of follow up. Comparisons are also performed in substudies defined by treatments modalités. Inflammatory parameters s ( CRP\_ C reactive protein, NLR- ( neutrophils to lymphocyte ratio) are measured on Day 0, 1, 8 and also salivary Immunoglobulins and different endocannabinoids.
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 by physicians in order to carefully compare side effects in the 3 armes of patients.. Our hypothesis was that hypnosis sedation generates less perioperative inflammatory reaction. A substudy of 50 patients was also dedicated to the investigation ofsalivary immunoglobulins and dosage of differents endocannabinoids
Interventions
PROCEDUREGeneral anesthesia
Patients will undergo oncologic breast surgery on general anesthesia.
PROCEDUREHypnosis sedation
Patients will undergo oncologic breast surgery on hypnosis sedation.
PROCEDUREGeneral anesthesia with preoperative session of hypnosis
Patients will undergo surgery on general anesthesia but will have a preoperative session of hypnosis relaxation.
Sponsors
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* 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 criteria
* 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of the days spent at the hospital post-surgery between the three groups | Day 0, 1, 8 and every 3 months for 2 years after surgery | The aim of the study is to compare the recovering period hospitalisation and the different side effects (pain, anxiety, fatigue and consumption of pain killers ) during the post opérative period ( day 0, 1, 8- and at each follow up visit) between a group of patients with conventional sedation, a group using hypnosis as sedation during the surgery and a third group using hypnosis as a relaxation method and preparation but enjoying a classic sedation for their surgery |
| Comparaison of inflammatory parameters measured on day 0,1,8: CRP ( c reactive protein) and NLR ( neutrophils to lymphocyte ratio) | Day 0, 1, 8 | Blood test performed |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Substudy evaluation of salivary immunoglobulins and endocannabinoids among 50 patients (25 under general anesthesia and 25 under hypnosis sedation | Simples collected on Day 0, 1 and 8 for endocannabinoids and salivary simples collected on Day 0 and 8 | Blood and salivary simples to observe if hypnosis modifies salivary parameters and endocannabinoids system |
Countries
Belgium
Outcome results
None listed