Alcoholism, Cancer of the Upper Aero-digestive Tract
Conditions
Keywords
alcohol addiction
Brief summary
The aim of the study is to compare the hospitalisation period in ORL surgery for two groups of patients. One of them will be treated for alcohol addiction to weaning them before the surgery ORL. The other group will be treated with usual methods.
Detailed description
Alcohol, associated or not associated with tobacco, is known to increase the incidence of ORL cancer. So, in fact many patients perform their ORL surgery operation in spite of their alcohol addiction. Many studies showed that a post surgery weaning syndrome increases morbidity and mortality. So our study will focuses on the benefits of pre surgery medical weaning program. The protocol is an open randomised, prospective study. The patient will be divided in two groups. In one hand, the first group is designed as treated will get alcohol weaning in the hospital alcohol department. The patient will be hospitalized during one week before the ORL surgery. During this hospitalisation, the patient will receive medicinal treatment, medical follow-up and psychological counselling. In the other hand, the second group designed as control group will be hospitalized directly in ORL surgery department. The patient will be received a treatment for alcohol weaning according to their symptom. After their hospitalisation, the treated group will be followed-up regularly for their alcohol addiction either in support group or in individual counselling. The control group will be followed-up with the usual method in the ORL surgery department. The expected result is to improve the care for patients with alcohol addiction and who must have an ORL surgery reducing the hospitalisation duration, the level of post operative complication and increasing the abstinence level. 115 patients will be included in this study.
Interventions
PROCEDUREHospitalization for a week
Patient in hospital a week before the date of surgery for the treatment of their addiction to alcohol (alcohol weaning)
Sponsors
National Cancer Institute, France
Department of Clinical Research and Innovation
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Age 18-80 years, male or female * Clinically and histologically verified ORL cancer required surgery * Patient with alcohol addiction * Men must consume 21 glasses of wine a week * Women must consume 14 glasses of wine a week * CPAM affiliation * Able to give written informed consent to participate in the study
Exclusion criteria
* Inability to give informed consent * Patient with regulatory authority or private patient freedom
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The primary endpoint of the study will be to compare the duration of post surgery hospitalisation between the patients who benefit with an alcohol weaning and the patient treated with usual methods. | two weeks | time between the surgery and the exit of the hospital |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objective is to note: the presence of weaning syndrome, the diagnostic of Delirium tremens, the occurrence of post surgeries complications. | two years |
Countries
France
Contacts
Primary ContactEve GELSI, MD
Backup ContactAlbert TRAN, PhD
Outcome results
None listed