Esomeprazole and Radiation Induced Esophagitis

Part of paid clinical trials in Chicago, Illinois.

Sponsor
Rush University Medical Center
Study ID
NCT06120803
Phase
PHASE2
Status
Recruiting

Conditions

  • Locally Advanced Lung Carcinoma
  • Radiation Esophagitis

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Esomeprazole 40 mg — DRUG
    Enrolled patients will receive 40 mg of esomeprazole (two pills of 20 mg strength of esomeprazole) once daily before breakfast for the entire duration of TRT (including the weekends and any interim gap period) and for two weeks after completion of thoracic radiation therapy.

Study Details

Thoracic radiation therapy combined with chemotherapy (with or without immunotherapy) is the cornerstone of management in patients with locally advanced non-small cell lung cancer (NSCLC).

Key Dates

Start date
Mar 1, 2024
Status verified
Apr 2025
Primary completion
Dec 30, 2027
Completion
Jun 30, 2028

Study Design

Enrollment
48 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Esomeprazole 40 mg daily with thoracic radiation therapy and concomitant chemotherapy
    Enrolled patients will receive 40 mg of esomeprazole (two pills of 20 mg strength of esomeprazole) once daily before breakfast for the entire duration of TRT (including the weekends and any interim gap period) and for two weeks after completion of thoracic radiation therapy (TRT). TRT will be delivered as per the discretion of the treating physicians.

Primary Outcome Measure

Grade 2 or higher radiation induced esophagitis [ Time Frame: At 2 weeks after completion of thoracic radiation therapy and at 3 months since start of radiation therapy ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Rush University Medical CenterChicagoIllinois60612
Soumyajit Roy, MD
312-942-5655

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