Evaluation of L-carnitine effect on prevention of chemotherapy-induced oral mucositis , A prospective, randomized, double-blind, controlled trial
Not Applicable
Recruiting
- Conditions
- mucositis.Oral mucositis (ulcerative)
- Registration Number
- IRCT201102265914N1
- Lead Sponsor
- Vice chancellor for research, Urmia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Exclusion criteria: the risk of side effects such as nausea or whenever the patient refuse to participate in the study
Inclusion criteria of the study: bedridden in Oncology unit, consent to participate in the study, without using drugs or any vitamin and mineral carnitine in the past 8 weeks, aged over 18 years
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oral mucositis. Timepoint: weekly. Method of measurement: observation.;CBC. Timepoint: weekly. Method of measurement: blood sample.
- Secondary Outcome Measures
Name Time Method