Status:
COMPLETED
Treatment of Chronic Itch in Patients Under Arsenic Exposure With Naloxone
Lead Sponsor:
Xiangya Hospital of Central South University
Conditions:
Chronic Pruritus
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief 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.
Detailed Description
This study aims to determine the efficacy and safety of sublingual naloxone in the treatment of chronic, refractory itch in patients under long-term arsenic exposure. In this study, 120 subjects with ...
Eligibility Criteria
Inclusion
- Aged 18 years or over and without diseases except arsenic-related pruritus
- Ability to study protocol and to give informed consent by himself/herself voluntarily
- The number of male or female subjects is required more than 1/3 of the total number of subjects
- Numeric Rating Sscale≥3 at the baseline
- Subjects taking hormone-containing medications must be on a stable dose for 6 months prior to study start to avoid any confounding influence on sensory and pain perception
Exclusion
- Use of oral anti-inflammatory medications for 2 weeks prior to the study start.
- Use of oral anti-histamines for 2 weeks prior to the study start.
- Use of topical or oral anti-pruritic agents for 2 weeks prior to the study start.
- Use of oral neuromodulatory agents for 2 months prior to study start.
- Current use of chronic pain medications (including opioids, antidepressants and anti-epileptic drugs).
- Use of nicotine-containing products for the past 6 months prior to study start.
- History of basic itchy dermatological diseases before such as eczema wich may influence the judgement of drug efficacy.
- Unstable thyroid function within the past 6 months prior to study start to exclude thyroid-related neuropathy.
- Known history of central or peripheral nervous system dysfunction.
- History of acute hepatitis, chronic liver disease or end stage liver disease.
- History of human immunodeficiency virus (HIV) or acquired immune deficiency syndrome.
- History of neuropathy associated with chronic obstructive pulmonary disease, diabetes mellitus, documented exposure to organophosphates or heavy metals or polychlorinated biphenyls.
- Known nutritional deficiency (vitamin B12, vitamin D, iron or zinc) within 3 months prior to the study start.
- Use of illicit drugs within the past 6 months prior to study start.
- Lyme disease, porphyria, rheumatoid arthritis, Hansen's disease (leprosy) or use of antineoplastic chemotherapeutic agents.
- Patients considered by researchers that are not suitable to the study.
Key Trial Info
Start Date :
February 13 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 30 2019
Estimated Enrollment :
126 Patients enrolled
Trial Details
Trial ID
NCT03751111
Start Date
February 13 2019
End Date
March 30 2019
Last Update
April 20 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Xiangya Hospital
Changsha, Hunan, China, 410008