Assessment of a topical retinoid effect in the treatment of a cutaneous side effect of chemotherapeutic agents
Phase 1
- Conditions
- hand-foot syndrome.localized skin eruption due to drugs and medicaments
- Registration Number
- IRCT201707163106N33
- Lead Sponsor
- Pharmaceutical Sciences branch, Islamic Azad University(a part of hanieh pourmousavi's PharmD thesis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Patients with hand-foot syndrome; Patients who 30 to 80 years old. Exclusion criteria: Skin infections; Skin cancer; Sensitivity to compounds of formula; Patient dissatisfaction
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of hand-foot syndrome. Timepoint: Beginning of the study, every 14 days, End of the study. Method of measurement: Common Terminology Criteria for Adverse Events.
- Secondary Outcome Measures
Name Time Method Skin Sensitivity. Timepoint: Beginning of the study, every 14 days, End of the study. Method of measurement: Observational.