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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Oral immunonutrition | Oral 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.