drugset / Trial / NCT03751111

Treatment of Chronic Itch in Patients Under Arsenic Exposure With Naloxone

NCT03751111

Phase 1/2 Completed 126 enrolled Xiangya Hospital of Central South University
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the efficacy and safety of sublingual naloxone in the treatment of chronic itch in patients under arsenic exposure.

Timeline

Start
2019-02-13
Primary completion
2019-03-01
Completion
2019-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Naloxone Small molecule 0.4 mg Subcutaneous

Indications

No indication recorded.