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Observational Trial on the Impact of Hypnose Used as a Sedation in Oncology Surgery in Breast Cancer

NCT03003611 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2017-11-13

No results posted yet for this study

Summary

The investigators will compare the operated patients for a beginning breast cancer in the Hypnose arm and the patient in the classical general anesthesia arm. It is a Observational study as we cannot randomized patient, (they need to be compliant with Hypnose).

Patient will be informed that some parameters, about his recovery, will be collected from their medical file. They will not have another particular treatment because they are in the study. It is just a prospective data collection.

The patient will be compared on several items after the surgery ( as pain and pain killer intake, the heal process of the scar, etc...) Also the investigators will compare the impact of hypnose on the other treatments the patient received.

The investigators need approximately 150 patients (Half in each arm).

Conditions

  • Early Stage Breast Carcinoma

Interventions

PROCEDURE

hypnose sedation

Patient will be anesthetized with an hypnose sedation and a complement with light anesthesia

PROCEDURE

general anesthesia

Patient will be anesthetized with a classical general anesthesia

Sponsors & Collaborators

  • Cliniques universitaires Saint-Luc- Université Catholique de Louvain

    lead OTHER

Principal Investigators

  • Martine Berlière, MD PhD · Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03003611 on ClinicalTrials.gov