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ACTIVE NOT RECRUITING
NCT04001543
NA

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

View on ClinicalTrials.gov

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

Interventions

DIETARY_SUPPLEMENT

Immunomodulating oral supplementation

Per os administration, 3 times / day, 5 days before each cycle of chemotherapy.

DIETARY_SUPPLEMENT

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