drugset / Trial / NCT03370367

Double Blind Phase III Trial of Effects of Low Dose 13-Cisretinoic Acid on Prevention of Second Primaries in Stages I-II Head and Neck Cancer

NCT03370367

Phase 3 Completed 189 enrolled Eastern Cooperative Oncology Group
RandomizedParallel-groupSingle-blindPrevention

Summary

In this trial the investigators propose to utilize 13-cRA to prevent dysplastic changes and second malignancies in patients with squamous cell carcinoma of the head and neck regions who have a high probability of cure from their primary cancer. Comparisons between patients treated by 13-cRA and patients receiving placebo will include: 1. The time to diagnosis of second primary for the treatment versus control groups. 2. Survival time for the treatment versus control groups. 3. Secondarily, the cost-benefit ratio for 13-cRA will be analyzed by assessing the toxicities of 13-cis retinoic acid treated patients in comparison to those experienced by placebo treated patients.

Timeline

Start
1989-05-15
Primary completion
1999-01-15
Completion
2015-04-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Isotretinoin Other / unclassified 3.75 mg
Subject Isotretinoin Other / unclassified 5 mg