Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06840704

Immunonutrition Reduces Acute Esophagitis After Thoracic Radiotherapy in Lung Cancer

Immunonutrition in Reducing Acute Esophagitis After Thoracic Radiotherapy in Lung Cancer: a Prospective, Randomized, Controlled, Open-label Clinical Trial

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
121 (estimated)
Sponsor
Hunan Cancer Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate the efficacy of immunonutrition in reducing acute esophagitis after thoracic radiotherapy in lung cancer.

Detailed description

This is a prospective, randomized, controlled, open-label clinical trial, which aimed to explore the efficacy and safety of oral immunonutrition therapy in reducing acute esophagitis after thoracic radiotherapy in lung cancer patients.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOral immunonutritionOral immunonutrition (Oral Impact®, Nestlé), 250 ml per bottle, with a dosage of 2 bottles per day, starting on the day of radiotherapy and continuing for three weeks after radiotherapy.

Timeline

Start date
2025-02-25
Primary completion
2026-06-30
Completion
2026-12-30
First posted
2025-02-21
Last updated
2026-04-02

Locations

6 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06840704. Inclusion in this directory is not an endorsement.