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Spots Global Cancer Trial Database for Alcohol Addiction and Otorhinolaryngology Cancer

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Trial Identification

Brief Title: Alcohol Addiction and Otorhinolaryngology Cancer

Official Title: Impact for Care for Patients With Alcohol Addiction and Treated for ORL Cancer

Study ID: NCT00825448

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Fédération des maladies de l'appareil digestif - Hôpital ARCHET, Nice, , France

Contact Details

Name: Albert TRAN, PhD

Affiliation: Centre Hospitalier Universitaire de Nice

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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