Evaluation the efficacy of topical naloxane on Controlling of Chronic Prupritus Induced By Chemical Injuries

Phase 2

• Conditions: Chronic Prupritus Induced By Chemical Injuries.; Irritant contact dermatitis; Pruritus; L24; L29

• Registration Number: IRCT201702221165N17
• Lead Sponsor: Baghiyatallah University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

1. self-satisfiction form should be filled by the patient; 2. the patients shouled be between 25-65 years old; 3. the Rx of pruritus induced by chemical gas shouled be diagnosed; 4. the patients shouldn’t have any other skin disorders; 5. the patients don’t use any topical steroids; 6. the patients shouldn’t be addict; 7. the patients be accessible; 8. the patients don’t leave the treatment more than one week; 9. the patients don’t have allergy to drug; 10. if the disease become uncontrolabe.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pruritus sevsrity. Timepoint: at the bigging off intervention,at the end of intervention. Method of measurement: standard questionaries.;Pruritus distribion. Timepoint: at the bigging off intervention,at the end of intervention. Method of measurement: standard questionaries.

Secondary Outcome Measures

Name	Time	Method
Pruritus frequency. Timepoint: at the bigging off intervention,at the end of intervention. Method of measurement: standard questionaries.;Pruritus period. Timepoint: at the bigging off intervention,at the end of intervention. Method of measurement: standard questionaries.;Quality of sleeping. Timepoint: at the bigging off intervention,at the end of intervention. Method of measurement: standard questionaries.