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Efficacy of an Oral Immunomodulatory Nutrient on Survival During Postoperative Concomitant Chemoradiotherapy in Head and Neck Cancer
Sponsor: Institut du Cancer de Montpellier - Val d'Aurelle
Summary
The investigators designed a prospective randomized double-blind trial to determine if the oral immunomodulating formula could improve the disease-free survival rate in high-risk locally-advanced head and neck Squamous Cell Carcinoma patients treated with Chemoradiotherapy.
Official title: Double-blind Multicenter Phase III Trial Evaluating the Efficacy of an Oral Immunomodulatory Nutrient on Survival During Postoperative Concomitant Chemoradiotherapy in Head and Neck Squamous Cell Carcinoma (HNSCC)
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
27
Start Date
2019-03-14
Completion Date
2026-05
Last Updated
2025-02-12
Healthy Volunteers
No
Conditions
Interventions
Immunomodulating oral supplementation
Per os administration, 3 times / day, 5 days before each cycle of chemotherapy.
Sip feed control
Per os administration, 3 times / day, 5 days before each cycle of chemotherapy.
Locations (2)
Centre Léon Bérard
Lyon, France
Institut du Cancer de Montpellier
Montpellier, France